each independently is a monovalent, divalent or trivalent hydrocarbon radical possessing from one to sixty carbon atoms other than from 2 to 8 carbon atoms.Priority:
Inventor: DUFFY JANET [US]; NICHOLSON JOHN [US]; WAHL ROY U R [US]
Application No.: US20070160549A1 Published: 12/Jul/2007Title: UV-radiation protectant compositions
Applicant/Assignee:
Application No.: 11/642492 Filing Date: 20/Dec/2006
Abstract:A substantially aqueous composition comprising one or more particle encapsulated sunscreen active agents, at least one volatile additive, and at least one UV-radiation scattering agent, whereby the composition provides an SPF greater than 30.
Priority: US20050752638P Applic. Date: 2005-12-21
Inventor: HUNT SHERI A [US]; FOWLER KEVIN C [US]; MEYER THOMAS A [US]
Application No.: US20070160551A1 Published: 12/Jul/2007Title: PENETRATING CARRIER, ANTI-FUNGAL COMPOSITION USING THE SAME AND METHOD FOR TREATMENT OF DERMATOPHYTES
Applicant/Assignee:
Application No.: 11/684869 Filing Date: 12/Mar/2007
Abstract:A liquid carrier for topical administration is provided that contains a mineral oil, turpentine and, optionally, camphor, and optionally other terpenoid components containing pinene, and its use to provide an antifungal composition a mixture of antifungal essential oils and the carrier system, wherein the mixture of antifungal essential oils includes an effective amount of each of eucalyptus globulus, peppermint, cedarwood, and Manuka
along with the use of this composition in the topical treatment of fungal infection, particularly of the nail.
Priority: US2004-956073 Applic. Date: 2004-10-04
Inventor: SELNER MARC [US]
Application No.: US20070160553A1 Published: 12/Jul/2007Title: Use of agents for the cosmetic treatment of keratin-containing material
Applicant/Assignee: WELLA AG
Application No.: 10/587278 Filing Date: 12/Jan/2005
Abstract:The object of the present invention is the use of a compound of formula and of the salts thereof in an agent for repairing, strengthening and restructuring keratin-containing material and protecting such material from mechanical and chemical damage.
Priority: DE200410013798 Applic. Date: 2004-03-20; WO2005EP01442 Applic. Date: 2005-02-12
Inventor: KRIPP THOMAS [DE]; GRASSER BEATE [DE]; SALLWEY ANETTE [DE]
Application No.: US20070160559A1 Published: 12/Jul/2007Title: Skin disinfectant composition and methods for using
Applicant/Assignee:
Application No.: 11/331410 Filing Date: 12/Jan/2006
Abstract:A skin disinfectant composition is provided according to the invention. The skin disinfectant composition comprises an effective amount of a disinfectant active component to provide disinfectant properties to skin tissue, an effective amount of a skin bonding polymer component to hold the disinfectant active component to skin tissue so that the disinfectant active component becomes available on skin tissue to provide disinfectant properties, and water. A method of using a skin disinfectant composition is provided.
Priority:
Inventor: ROSZELL JAMES A [US]
Application No.: US20070160576A1 Published: 12/Jul/2007Title: IL-17A/F heterologous polypeptides and therapeutic uses thereof
Applicant/Assignee: GENENTECH, INC
Application No.: 11/606192 Filing Date: 29/Nov/2006
Abstract:The present invention is directed to a novel naturally occurring human cytokine that is comprised of a heterodimer of interleukin-17 and interleukin-17F designated herein as interleukin 17A/F (IL-17A/F). Also provided herein are vectors and host cells comprising those nucleic acid sequences, chimeric polypeptide molecules comprising the polypeptides of the present invention fused to heterologous polypeptide sequences, specific antibodies which bind to the polypeptides of the present invention and to methods for producing the polypeptides of the present invention. Further provided herein are methods for treating degenerative cartilaginous disorders and other inflammatory diseases.
Priority: US2004-860824 Applic. Date: 2004-06-02; WO2004US17581 Applic. Date: 2004-06-02; US2001-000157 Applic. Date: 2001-10-30; US2001-874503 Applic. Date: 2001-06-05; US20030485599P Applic. Date: 2003-07-08; US20030486457P Applic. Date: 2003-07-11
Inventor: ARNOTT DAVID P [US]; BALAZS MERCEDESZ [US]; GHILARDI NICO [US]; GURNEY AUSTIN L [US]; HASS PHILIP E [US]; HYMOWITZ SARAH [US]; LEE JAMES M [US]; OUYANG WENJUN [US]; STAROVASNIK MELISSA A [US]; WU YAN [US]
Application No.: US20070160586A1 Published: 12/Jul/2007Title: Methods for extending the replicative lifespan of cells
Applicant/Assignee: CHILDREN'S MEDICAL CENTER CORPORATION
Application No.: 11/453283 Filing Date: 14/Jun/2006
Abstract:The present invention is directed to methods for enhancing the replicative capacity of cells, by culturing the cells in the presence of an active agent or compound which inhibits SIRT1. One method provides expanding stem cells by culturing the cells in the presence of a SIRT1 inhibitor. The resulting cultured cells can be used for a variety of applications including cell-based therapies such as bone marrow transplants, gene therapies, tissue engineering, and in vitro organogenesis.
Priority: US20050690609P Applic. Date: 2005-06-15
Inventor: ALT FREDERICK W [US]; LOMBARD DAVID B [US]; CHUA KATRIN F [US]; MOSTOSLAVSKY RAUL [US]; CHENG HWEI-LING [US]
Application No.: US20070160653A1 Published: 12/Jul/2007Title: Hemostatic textile
Applicant/Assignee:
Application No.: 11/650670 Filing Date: 08/Jan/2007
Abstract:The present invention is directed to a hemostatic textile, comprising: a material comprising a combination of glass fibers and one or more secondary fibers selected from the group consisting of silk fibers
ceramic fibers
raw or regenerated bamboo fibers
cotton fibers
rayon fibers
linen fibers
ramie fibers
jute fibers
sisal fibers
flax fibers
soybean fibers
corn fibers
hemp fibers
lyocel fibers
wool
lactide and/or glycolide polymers
lactide/glycolide copolymers
silicate fibers
polyamide fibers
feldspar fibers
zeolite fibers, zeolite-containing fibers, acetate fibers
and combinations thereof
the hemostatic textile capable of activating hemostatic systems in the body when applied to a wound. Additional cofactors such as thrombin and hemostatic agents such as RL platelets, RL blood cells
fibrin, fibrinogen, and combinations thereof may also be incorporated into the textile. The invention is also directed to methods of producing the textile, and methods of using the textile to stop bleeding.
Priority: US20060758261P Applic. Date: 2006-01-11
Inventor: FISCHER THOMAS H [US]; ESKRIDGE E S JR [US]; MALLOY WILLIAM M JR [US]; EVANS MALLOY [US]
Application No.: US20070161526A1 Published: 12/Jul/2007Title: SOLUBILIZING SYSTEMS FOR FLAVORS AND FRAGRANCES
Applicant/Assignee: FIRMENICH SA
Application No.: 11/689635 Filing Date: 22/Mar/2007
Abstract:The present invention provides compositions and clear oil-in-water microemulsion containing up to 80% w/w of an oil, a surfactant system, a w/w oil/surfactant system ratio between 1 and 3, and a solubilizing-aid ingredient which is not a surfactant neither a VOC compound, the latter being present in an amount sufficient to ensure that the ratio oil/(surfactant+solubilizing-aid) is between 0.1 and 5. The present invention concerns also the articles and products associated with such compositions and microemulsions, and the methods to manufacture them.
Priority: EP20040105185 Applic. Date: 2004-10-20; WO2005IB03329 Applic. Date: 2005-10-19; US20040620557P Applic. Date: 2004-10-20
Inventor: VLAD FLORIN J [US]; MOUNIER REMY [FR]; WONG KENNETH [CH]; DAUGERON AUDE [FR]; HERD THOMAS [US]
Application No.: US20070161527A1 Published: 12/Jul/2007Title: Dispersions
Applicant/Assignee: DISPERSE LIMITED
Application No.: 10/586328 Filing Date: 18/Jan/2005
Abstract:A solid composition comprising oil core aphrons dispersed in a solid surfactant.
Priority: GB20040001101 Applic. Date: 2004-01-19; WO2005GB00162 Applic. Date: 2005-01-18
Inventor: MERCURIO ANTHONY F [US]; WHEELER DEREK A [GB]
Application No.: US20070161543A1 Published: 12/Jul/2007Title: N-(PHOSPHONOALKYL)-AMINO ACIDS, DERIVATIVES THEREOF AND COMPOSITIONS AND METHODS OF USE
Applicant/Assignee:
Application No.: 11/621287 Filing Date: 09/Jan/2007
Abstract:The present invention relates to an N-(phosphonoalkyl)-amino acid, a related compound or a derivative thereof, the N-(phosphonoalkyl)-amino acid, related compound or derivative thereof being in a form as a free acid, salt, partial salt, lactone, amide or ester, or in stereoisomeric or non-stereoisomeric form, other than N-(phosphonomethyl)-glycine or N,N-bis(phosphonomethyl)-glycine.
Also included is a composition including an N-(phosphonoalkyl)-amino acid, a related compound or a derivative thereof in a form as a free acid, salt, partial salt, lactone, amide or ester, or in stereoisomeric or non-stereoisomeric form, and a cosmetically or pharmaceutically acceptable vehicle for topical or systemic administration to a mammalian subject, as well as a method of administering an effective amount of such a composition for alleviating or improving a condition, disorder, symptom or syndrome associated with at least one of a nervous, vascular, musculoskeletal or cutaneous system.
Priority: US20060757614P Applic. Date: 2006-01-10
Inventor: YU RUEY J [US]; VAN SCOTT EUGENE J [US]
Application No.: US20070161552A1 Published: 12/Jul/2007Title: Use of low-dosage erythropoietin for stimulation of endothelial progenitor cells, for organ regeneration and for slowing the progression of end-organ damage
Applicant/Assignee:
Application No.: 10/586896 Filing Date: 22/Jan/2005
Abstract:The present invention relates to the use of low-dosage erythropoietin for stimulation of physiological mobilization, proliferation and differentiation of endothelial progenitor cells, for stimulation of vasculogenesis, for therapy of diseases related to a dysfunction of endothelial progenitor cells, and for production of pharmaceutical compositions for treatment of such diseases as well as pharmaceutical compositions that include erythropoietin and other suitable active ingredients for stimulation of endothelial progenitor cells.
Priority: DE200410004509 Applic. Date: 2004-01-23; WO2005EP00618 Applic. Date: 2005-01-22
Inventor: BAHLMANN FERDINAND H [DE]; HALLER HERMANN [DE]
Application No.: US20070161645A1 Published: 12/Jul/2007Title: Thiazole inhibitors targeting resistant kinase mutations
Applicant/Assignee: TARGEGEN, INC
Application No.: 11/591252 Filing Date: 31/Oct/2006
Abstract:A compound is provided, having the general structure (A): wherein A is an aryl or heteroaryl group, Y is a hydrophbic linking moiety, and L is a substitutent. The compound (A) can be used for treatment of various angiogenic-associated or hematologic disorders, such as myeloproliferative disorders in patients who do not respond to kinase-inhibition therapy that comprises administering currently used medications.
Priority: US20050733115P Applic. Date: 2005-11-02
Inventor: NORONHA GLENN [US]; CAO JIANGUO [US]; ZENG BINQI [US]; MAK CHI C [US]; MCPHERSON ANDREW [US]; RENICK JOEL [US]; PATHAK VED P [US]; CHOW CHUN [US]; PALANKI MOORTHY [US]; SOLL RICHARD M [US]; LOHSE DANIEL L [US]; HOOD JOHN D [US]; DNEPROVSKAIA ELENA [US]
Application No.: US20070161681A1 Published: 12/Jul/2007Title: ETHER DERIVATIVES USEFUL AS INHIBITORS OF PDE4 ISOZYMES
Applicant/Assignee: PFIZER PRODUCTS INC
Application No.: 11/668915 Filing Date: 30/Jan/2007
Abstract:Compounds useful as inhibitors of PDE4 in the treatment of diseases regulated by the activation and degranulation of eosinophils, especially asthma, chronic bronchitis, and chronic obstructive pulmonary disease, of the formula: wherein the substituents are as defined in the specification.
Priority: US2004-918820 Applic. Date: 2004-08-13; US2002-066503 Applic. Date: 2002-01-31; US20010265304P Applic. Date: 2001-01-31
Inventor: MARFAT ANTHONY [US]; CHAMBERS ROBERT J [US]; MAGEE THOMAS V [US]
Application No.: US20070161696A1 Published: 12/Jul/2007Title: Methods of using and compositions comprising selective cytokine inhibitory drugs for treatment, modification and management of pain
Applicant/Assignee:
Application No.: 10/576139 Filing Date: 23/Apr/2004
Abstract:Methods of treating, preventing, modifying and managing various types of pain are disclosed. Specific methods comprise the administration of a selective cytokine inhibitory drug, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof, alone or in combination with a second active agent and/or surgery, psychological or physical therapy. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in methods of the invention are also disclosed.
Priority: WO2004US12722 Applic. Date: 2004-04-23
Inventor: ZELDIS JEROME B [US]; FALECK HERBERT [US]; MANNING DONALD C [US]
Application No.: US20070166248A1 Published: 19/Jul/2007Title: Aqueous photoprotective compositions comprising hydrophilic metal oxide nanopigments and polyalkylene glycols of low molecular mass
Applicant/Assignee: L'OREAL
Application No.: 11/653394 Filing Date: 16/Jan/2007
Abstract:Stable, reduced whitening photoprotective compositions contain: a) at least one aqueous phase, b) at least hydrophilic inorganic nanopigments based on metal oxides, in an amount ranging from 1% to 25% by weight, with respect to the total weight of the composition, and c) at least one polyalkylene glycol having a molecular mass of less than 8,000 g/mol, formulated into d) a topically applicable, physiologically acceptable medium therefor.
Priority: FR20040051508 Applic. Date: 2004-07-13; WO2005EP07887 Applic. Date: 2005-06-13
Inventor: L ALLORET FLORENCE [FR]; SIMONNET JEAN-THIERRY [FR]
Application No.: US20070166251A1 Published: 19/Jul/2007Title: Composition and method for treating hyperpigmented skin
Applicant/Assignee: LIPO CHEMICALS INC
Application No.: 11/643562 Filing Date: 20/Dec/2006
Abstract:An improved cosmetic and dermatological composition and a method for treating hyperpigmented skin is disclosed. The composition demonstrates an enhanced ability to lighten mammalian skin color, and is nontoxic and nonirritating. The composition comprises a hydroxycinnamic acid or a methoxycinnamic acid dissolved in a compound having one or more hydroxy groups, like a PEG-4 through PEG-20, a monoC1-4alkyl ether of an ethylene glycol, or a monoC1-4alkyl ether of a propylene glycol oligomer, and/or a silicone fluid.
Priority: WO2005US46175 Applic. Date: 2005-12-20; US20050643797P Applic. Date: 2005-01-14; US20050652303P Applic. Date: 2005-02-11
Inventor: DAYAN NAVA [US]; RIEMER JED A [US]
Application No.: US20070166252A1 Published: 19/Jul/2007Title: Method of treating skin requiring tattoo removal
Applicant/Assignee:
Application No.: 11/648290 Filing Date: 29/Dec/2006
Abstract:A treatment regimen for treating skin subject to tattoo removal procedures involves the application of supplemental composition(s) such as preparatory composition(s), protective composition(s), and combinations thereof, and a corrective composition.
Priority: US20050755357P Applic. Date: 2005-12-30
Inventor: HATTENDORF JUDY [US]; CARLSON STEVE [US]
Application No.: US20070166254A1 Published: 19/Jul/2007Title: ANTIPERSPIRANT STICK COMPOSITIONS
Applicant/Assignee: CONOPCO, INC., D/B/A UNILEVER
Application No.: 11/622682 Filing Date: 12/Jan/2007
Abstract:Disclosed are antiperspirant stick compositions comprising specified amounts of antiperspirant active
carrier oil comprising volatile silicone oil and non-volatile masking oil
structurant comprising fatty alcohol and cosmetically acceptable wax having a melting point of 75 to 95 DEG C., a portion of wax comprises polyethylene in specified amounts. Also disclosed are methods of making such stick compositions, and methods of ameliorating perspiration by the topical application of such compositions to the skin.
Priority: US20060758895P Applic. Date: 2006-01-14
Inventor: BIANCHI JAMES M [US]
Application No.: US20070166337A1 Published: 19/Jul/2007Title: Skincare compositions and methods
Applicant/Assignee: BOOTS HEALTHCARE INTERNATIONAL LIMITED
Application No.: 10/571757 Filing Date: 10/Sep/2004
Abstract:There is disclosed a skincare composition suitable for topical application to the skin. The composition comprises from 0.5 to 10% by weight of salicylic acid and from 0.5 to 10% of hydrogen peroxide, but is substantially free of other therapeutic agents selected from the group consisting of anti-microbial agents, anti-bacterial agents, anti-viral agents, anti-fungal agents, anthelmintic agents and anti-inflammatory agents. The composition is useful in the treatment of acne.
Priority: GB20030021541 Applic. Date: 2003-09-13; GB20040003702 Applic. Date: 2004-02-19; GB20040019260 Applic. Date: 2004-08-31; WO2004GB03879 Applic. Date: 2004-09-10
Inventor: TREUDLER KLAUS [DE]; MALLWITZ HENNING [US]; SCHMIDT TIMM [US]; EVISON JANE [US]
Application No.: US20070166339A1 Published: 19/Jul/2007Title: Skin Whitening Methods and Compositions Based on Zeolite - Active Oxygen Donor Complexes
Applicant/Assignee: BIODERM RESEARCH
Application No.: 11/684702 Filing Date: 12/Mar/2007
Abstract:The present invention discloses certain complexes of anionic zeolites with active oxygen donor agents, such as organic or inorganic peroxides, and methods and compositions based on said complexes for skin whitening.
Priority: US2004-710011 Applic. Date: 2004-06-11; US2006-307824 Applic. Date: 2006-02-24; US2003-418495 Applic. Date: 2003-04-18
Inventor: GUPTA SHYAM K [US]
Application No.: US20070166359A1 Published: 19/Jul/2007Title: HoxD3, HoxA3 and HoxB3 compositions and methods for improved wound healing
Applicant/Assignee: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Application No.: 11/648208 Filing Date: 29/Dec/2006
Abstract:The present invention provides methods and compositions useful in localized transfer of genetic material or proteins. Moreover, the present invention provides methods and compositions for improving and/or controlling wound healing by applying a wound care device comprising HoxD3 and/or HoxA3 and/or HoxB3. In addition, the present invention provides methods and compositions for improved wound healing in subjects having impaired healing capabilities, such as diabetic and aged subjects.
Priority: US2003-746592 Applic. Date: 2003-12-23; US2002-305667 Applic. Date: 2002-11-26; WO2002US19020 Applic. Date: 2002-06-14; US20010307632P Applic. Date: 2001-07-24; US20010298688P Applic. Date: 2001-06-14
Inventor: BOUDREAU NANCY [US]; YOUNG DAVID M [US]; MYERS CORNELIA [US]
Application No.: US20070166405A1 Published: 19/Jul/2007Title: Extracts of houttuynia cordata and rubus coreanus and their composition for preventing and treating allergic diseases
Applicant/Assignee: REGEN BIOTECH INC
Application No.: 10/587677 Filing Date: 04/Feb/2005
Abstract:The present invention relates to an extract of Houttuynia cordata and Rubus coreanus, and a composition for the prevention and treatment of allergic diseases, comprising the same. The inventive extract and the composition comprising the same have the effect of preventing and treating allergic diseases by inhibiting the degranulation and histamine release of mast cells. Also, they show no cytotoxicity and thus can be safely use in vivo.
Priority: KR20040007404 Applic. Date: 2004-02-05; WO2005KR00339 Applic. Date: 2005-02-04
Inventor: SONG CHANG-HO [KR]; CHAI OK-HEE [KR]; PARK YONG-IN [KR]; LEE DONG-SIN [KR]
Application No.: US20070167426A1 Published: 19/Jul/2007Title: Compounds for the treatment of inflammatory disorders and microbial diseases
Applicant/Assignee: SCHERING CORPORATION
Application No.: 11/599784 Filing Date: 15/Nov/2006
Abstract:This invention relates to compounds of the Formula (I): or a pharmaceutically acceptable salt, solvate or isomer thereof, which can be useful for the treatment of diseases or conditions mediated by MMPs, aggrecanase, ADMP, LpxC, ADAMs, TACE, TNF-alpha or combinations thereof.
Priority: US2005-291595 Applic. Date: 2005-12-01; US2005-142601 Applic. Date: 2005-06-01; US20040576153P Applic. Date: 2004-06-02
Inventor: SIDDIQUI M A [US]; MANSOOR UMAR F [US]; REDDY PANDURANGA A P [US]; MADISON VINCENT S [US]
Application No.: US20070167468A1 Published: 19/Jul/2007Title: SUBSTITUTED BICYCLIC 8-PYRR0LIDINOXANTHINES, METHODS FOR THEIR PRODUCTION, PHARMACEUTICAL FORMULATIONS AND THEIR USE
Applicant/Assignee: SANOFI-AVENTIS DEUTSCHLAND GMBH
Application No.: 11/623770 Filing Date: 17/Jan/2007
Abstract:Compounds for the treatment of elevated blood glucose levels and the physiological and metabolic disorders arising therefrom are disclosed and comprise novel substituted bicyclic 8-pyrrolidinoxanthines and their derivatives of formula l: wherein the various R groups are hereinafter defined. The present invention also comprises pharmaceutical compositions comprising them as well as processes for the preparation of these compounds. Particular blood glucose disorders treatable thereby include type-2 diabetes, insulin resistance, hyperglycemia, arteriosclerotic diseases and the like.
Priority: DE200410038270 Applic. Date: 2004-08-06; WO2005EP08005 Applic. Date: 2005-07-22
Inventor: SCHOENAFINGER KARL [DE]; JAEHNE GERHARD [DE]; DEFOSSA ELISABETH [DE]; SCHWINK LOTHAR [DE]; WAGNER HOLGER [DE]; BUNING CHRISTIAN [DE]; TSCHANK GEORG [DE]; WERNER ULRICH [DE]
Application No.: US20070167495A1 Published: 19/Jul/2007Title: Pleuromutilin derivatives, process for their preparation and uses thereof
Applicant/Assignee: GLAXOSMITHKLINE SERVICES UNLIMITED
Application No.: 10/552238 Filing Date: 06/Apr/2004
Abstract:Pleuromutilin compounds of the formula: are of use in antibacterial therapy.
Priority: GB20030008114 Applic. Date: 2003-04-08; WO2004EP03783 Applic. Date: 2004-04-06
Inventor: BROWN PAMELA [GB]; HUNT ERIC [GB]
Application No.: US20070167517A1 Published: 19/Jul/2007Title: Stabilized derivatives of ascorbic aicd
Applicant/Assignee: TAGRA BIOTECHNOLOGIES LTD
Application No.: 10/553757 Filing Date: 21/Apr/2004
Abstract:Ascorbic acid derivatives of the general formula 1: wherein R<1> is a C2-C22 acyl group, an amino acid group, or a C1-C17 alkyl group
R<2> is ammonium or a metal cation
and each of R<3> or R<4>, independently, is hydrogen, a C2-C22 acyl group, an amino acid residue, or a C1-C17 alkyl group, are more stable than ascorbic acid and can be used as a source of vitamin C in pharmaceutical, nutraceutical and cosmetic compositions.
Priority: US20030464097P Applic. Date: 2003-04-21; WO2004IL00343 Applic. Date: 2004-04-21
Inventor: KVITNITSKY EMMA [IL]; BELAKHOV VALERY [IL]; BABTSOV VLADIMIR [IL]; SHAPIRO VURY [IL]
Application No.: US20070172436A1 Published: 26/Jul/2007Title: Nonaqueous ascorbic acid compositions and methods for preparing same
Applicant/Assignee:
Application No.: 11/337786 Filing Date: 23/Jan/2006
Abstract:A method for preparing a nonaqueous ascorbic acid composition in an alcohol solvent comprising ascorbic acid, a solubilization enhancer, and an oleaginous skin protectant is described. The amount of ascorbic acid dissolved in the nonaqueous composition in the presence of the solubilization enhancer is greater than the amount of ascorbic acid that would be soluble in the solvent in the absence of the solubilization enhancer. A nonaqueous composition comprises the dissolved ascorbic acid, solubilization enhancer, and homogenized oleaginous skin protectant.
Priority:
Inventor: ZHANG JERRY [US]
Application No.: US20070172464A1 Published: 26/Jul/2007Title: Stem cells having increased sensitivity to a chemoattractant and methods of generating and using same
Applicant/Assignee: YEDA RESEARCH AND DEVELOPMENT CO., LTD
Application No.: 10/552331 Filing Date: 07/Apr/2004
Abstract:The present invention relates to stem cells which exhibit increased sensitivity to a chemoattractant and, more particularly, to methods of generating and using them such as in clinical applications involving stem cell transplantation.
Priority: IL20030155303 Applic. Date: 2003-04-08; IL20030159307 Applic. Date: 2003-12-10; WO2004IL00315 Applic. Date: 2004-04-07
Inventor: KOLLET ORIT [IL]; LAPIDOT TSVEE [IL]
Application No.: US20070172516A1 Published: 26/Jul/2007Title: Increasing of the resorption of substances via skin and mucous membranes
Applicant/Assignee: PROCOM BIOTECHNOLOGISCHE PRODUKTIONS GMBH
Application No.: 10/526846 Filing Date: 03/Sep/2003
Abstract:The invention relates to the increasing of the resorption of substances via skin and mucous membranes. The invention also relates to substances having an increased capability of being resorbed by skin and mucous membranes, and to pharmaceutical compositions containing substances of this type.
Priority: DE20021040894 Applic. Date: 2002-09-04; WO2003EP09788 Applic. Date: 2003-09-03
Inventor: PODSCHUN TRUTZ [DE]; HOFSCHNEIDER PETER H [DE]; HILDT EBERHARD [DE]
Application No.: US20070173482A1 Published: 26/Jul/2007Title: Agents for preventing and treating disorders involving modulation of the RyR receptors
Applicant/Assignee: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Application No.: 11/506285 Filing Date: 17/Aug/2006
Abstract:The present invention provides compounds of Formula I and salts, hydrates, solvates, complexes, and prodrugs thereof. The present invention further provides methods for synthesizing compounds of Formula I. The invention additionally provides pharmaceutical compositions comprising the compounds of Formula I and methods of using the pharmaceutical compositions of Formula I to treat and prevent disorders and diseases associated with the RyR receptors that regulate calcium channel functioning in cells.
Priority: US2005-212309 Applic. Date: 2005-08-25
Inventor: MARKS ANDREW R [US]; LANDRY DONALD W [US]; DENG SHIXIAN [US]
Application No.: US20070178051A1 Published: 02/Aug/2007Title: STERILIZED NANOPARTICULATE GLUCOCORTICOSTEROID FORMULATIONS
Applicant/Assignee: ELAN PHARMA INTERNATIONAL, LTD
Application No.: 11/275775 Filing Date: 27/Jan/2006
Abstract:The invention is directed sterile to compositions of glucocorticosteroids useful in the prophylaxis and chronic treatment of asthma and other allergic and inflammatory conditions in adults and pediatric patients.
Priority:
Inventor: PRUITT JOHN [US]; KEWALRAMANI RAJ [US]; SLIFER DAVID [US]; SHAW JACK M [US]; RUDDY STEPHEN B [US]
Application No.: US20070178053A1 Published: 02/Aug/2007Title: Antiperspirant compositions
Applicant/Assignee: CONOPCO INC, D/B/A UNILEVER
Application No.: 11/698392 Filing Date: 26/Jan/2007
Abstract:Antiperspirant water in oil emulsions can suffer from inferior sensory properties, including wetness and/or slow "dry-down" and/or stickiness, even when the composition contains a polyhydric humectant, a known class of skin moisturiser. A balance of sensory properties can be achieved by formation of a base composition in the form of a water in oil emulsion in which the oil phase, preferably comprising 20 to 55% of the base composition, contains at least threshold proportions of both a volatile silicone and a sensory modifying oil, particularly selected from dicaprylyl ether and dicaprylyl carbonate, the sensory modifying oil advantageously being present in a weight ratio to the polyhydric humectant of from 3:4 to 4:1. Such compositions are particularly suitable for mixture with a liquifiable propellant to form aerosol compositions.
Priority: GB20060001644 Applic. Date: 2006-01-27
Inventor: FRANKLIN KEVIN RONALD [GB]; IRVOAS ANNE-CECILE MARIE EUGEN [GB]
Application No.: US20070178057A1 Published: 02/Aug/2007Title: High efficiency sunscreen composition particularly useful for wipes and sprays
Applicant/Assignee: AMCOL INTERNATIONAL CORPORATION
Application No.: 11/345064 Filing Date: 01/Feb/2006
Abstract:A sunscreen composition, either impregnating a wipe substrate or comprising a sunscreen spray, wherein the composition comprises an oil phase dispersed stably as emulsion droplets in a water phase that contains i) a booster for the sun protection factor (SPF), comprising a combination of water-dispersible particulate materials, one of which is smectite clay, and a water-soluble or water-dispersible phenolic polymer
and ii) a water-soluble or water-dispersible polymer having a weak acid group, a weight average molecular weight of 1,000-100,000 Dalton, and an anionic charge density of no less than 4 milliequivalent per gram of the polymer
the said sunscreen composition meeting the following specifications: i) the in-vivo sun protection factor (SPF) is >=1.8 times the weight percent of the sunscreen active(s) contained therein, based on the weight of the sunscreen composition
and ii) the shear thinning index of the composition is greater by 5% or higher with the weak acid polymer contained therein than without the polymer, the shear thinning index being defined as the ratio of viscosities of the sunscreen composition at 0.5 rpm and 20 rpm, measured on a Brookfield RVT viscometer at 25 DEG C., using spindle 7, after cooling the composition to room temperature and storing it at that temperature for about 24 hours.
Priority:
Inventor: SENGUPTA ASHOKE K [US]; CURETON KEVIN [US]; LIN ILONA [US]; BEIHOFFER THOMAS W [US]
Application No.: US20070178059A1 Published: 02/Aug/2007Title: Cosmetic and pharmaceutical uses of an extract of a plant belonging to the genus buchholzia
Applicant/Assignee:
Application No.: 10/593850 Filing Date: 15/Mar/2005
Abstract:A cosmetic or dermopharmaceutical composition including an extract of a plant belonging to the genus Buchholzia and at least one auxiliary and/or additive is provided. A method for the cosmetic treatment of the skin or scalp and a method for the treatment of skin inflammation includes administering to a patient in need thereof a composition including an effective amount of a plant extract from a plant belonging to the genus Buchholzia.
Priority: EP20040290788 Applic. Date: 2004-03-24; WO2005EP02729 Applic. Date: 2005-03-15
Inventor: MOSER PHILIPPE [FR]; DANOUX LOUIS [FR]; PAULY GILLES [FR]
Application No.: US20070178066A1 Published: 02/Aug/2007Title: PATHOTROPIC TARGETED GENE DELIVERY SYSTEM FOR CANCER AND OTHER DISORDERS
Applicant/Assignee:
Application No.: 11/556666 Filing Date: 03/Nov/2006
Abstract:Systems for pathotropic (disease-seeking) targeted gene delivery are provided, including viral particles with extremely high titers. In particular, the viral particles are engineered to specifically deliver therapeutic or diagnostic agents to a disease site, such as cancer metastic sites. Personalized dosing regimens are also provided to treat diseases such as cancer efficaciously with reduced adverse side effects.
Priority: US2004-829926 Applic. Date: 2004-04-21; US20030464571P Applic. Date: 2003-04-21
Inventor: HALL FREDERICK L [US]; LEVY JOHN P [US]; REED REBECCA A [US]; GORDON ERLINDA M [US]
Application No.: US20070178082A1 Published: 02/Aug/2007Title: Stabilized single domain antibodies
Applicant/Assignee: ABLYNX N.V
Application No.: 10/534349 Filing Date: 07/Nov/2003
Abstract:The present invention relates to heterospecific polypeptide constructs comprising at least one single domain antibody directed against a therapeutic and/or diagnostic target and at least one single domain antibody directed against a serum protein, said construct having a prolonged lifetime in biological circulatory systems. The invention further relates to methods for stabilising VHHs in biological circulatory systems.
Priority: EP20030447005 Applic. Date: 2003-01-10; WO2003EP06581 Applic. Date: 2003-06-23; WO2003EP07313 Applic. Date: 2003-07-08; US20020425073P Applic. Date: 2002-11-08; US20020425063P Applic. Date: 2002-11-08; WO2003BE00193 Applic. Date: 2003-11-07
Inventor: SILENCE KAREN [BE]; LAUWEREYS MARC [BE]; DREIER TORSTEN [DE]
Application No.: US20070178202A1 Published: 02/Aug/2007Title: Method for recovering a secondary plant metabolite
Applicant/Assignee: ROYAL SCHOUTEN GROUP N.V
Application No.: 10/551171 Filing Date: 22/Apr/2004
Abstract:The present invention relates to a method for recovering a secondary plant metabolite from a seed material. The present invention further relates to a extract comprising the secondary plant metabolite, which extract is obtainable by a method according to the invention and to a foodstuff, cosmetic or medicament comprising such an extract.
Priority: EP20030076175 Applic. Date: 2003-04-22; US20030464451P Applic. Date: 2003-04-22; WO2004NL00268 Applic. Date: 2004-04-22
Inventor: VERBRUGGEN MARIA A [NL]; BAKKER RUDOLF WILHELMUS M [NL]
Application No.: US20070179241A1 Published: 02/Aug/2007Title: Compositions having improved soft focus effect properties
Applicant/Assignee: L'OREAL
Application No.: 11/342913 Filing Date: 31/Jan/2006
Abstract:The invention relates to a composition, especially a cosmetic composition, containing at least one silicone elastomer and at least one encapsulated pigment, wherein the refractive index of the pigment is greater than the refractive index of the encapsulating material.
Priority:
Inventor: PATEL DHAVAL [US]
Application No.: US20070181913A1 Published: 09/Aug/2007Title: Integrated Circuit Device
Applicant/Assignee:
Application No.: 11/381348 Filing Date: 02/May/2006
Abstract:A commercially mass-produced, integrated circuit including: a solid substrate of one conductivity type
at least one solid material pocket of a different conductivity type having a side surface and positioned on a selected top surface of the substrate to thereby form a signal-translating, electronic rectifying barrier between the at least one solid material pocket and the selected top surface of the substrate
and a solid state material region adjoining the substrate, the electronic rectifying barrier, and the side surface of the at least one solid material pocket
wherein next to the electronic rectifying barrier the solid state material region has a lateral dimensional accuracy of better than a few hundred atomic layers.
Priority: US2004-759081 Applic. Date: 2004-01-20; US1995-483938 Applic. Date: 1995-06-07
Inventor: LI CHOU H [US]
Application No.: US20070183992A1 Published: 09/Aug/2007Title: Cosmetic composition comprising porous particles incorporating optically active substances
Applicant/Assignee: L'OREAL
Application No.: 10/566965 Filing Date: 05/Aug/2004
Abstract:An object of the invention is to offer an optical additive capable of adequately activating the effects of incorporated optically active substances, providing the base with such optical effects, having a suitable sensation and level of safety, and having exceptional cosmetic properties. A cosmetic composition comprising in a physiologically acceptable medium (a) silicium based porous particles having an aspect ratio of at least 2 and (b) an optically active substance incorporated into said porous particles is offered. The incorporated optically active substances are selected from among UV screening substances, fluorescent substances and photochromic substances.
Priority: JP20030286827 Applic. Date: 2003-08-05; WO2004JP11626 Applic. Date: 2004-08-05
Inventor: DUMOUSSEAUX CHRISTOPHE [JP]; GOTO TATSUNARI [JP]
Application No.: US20070183993A1 Published: 09/Aug/2007Title: Personal care compositions
Applicant/Assignee:
Application No.: 11/638255 Filing Date: 13/Dec/2006
Abstract:Personal care compositions comprising a PPARG antagonist, use of such compositions, and methods of marketing such compositions. The personal care compositions can be applied topically, ingested orally, injected, or used as part of a regimen.
Priority: US20050749911P Applic. Date: 2005-12-13
Inventor: BINDER ROBERT L [US]; SREEKRISHNA KOTIKANYADANAM [US]; EICKHOFF DAVID J [US]; ROBINSON LARRY R [US]; OSBORNE ROSEMARIE [US]
Application No.: US20070183995A1 Published: 09/Aug/2007Title: Compounds useful as agonists of A2A adenosine receptors, cosmetic compositions with A2A agonists and a method for using the same
Applicant/Assignee: CONOPCO, INC., D/B/A UNILEVER
Application No.: 11/350658 Filing Date: 09/Feb/2006
Abstract:Compounds useful as agonists of A2A adenosine receptors are described. Also described is a cosmetically acceptable composition having an agonists of A2A adenosine receptors where the composition is suitable to apply to human skin to reduce the effects of melanin, resulting in skin whitening.
Priority:
Inventor: NIP JOHN C [US]; BOSKO CAROL A [US]; ROSA JOSE G [US]; HARICHIAN BIJAN [US]; SANTANA ISABEL C [US]
Application No.: US20070183996A1 Published: 09/Aug/2007Title: Para-coumaric acid or para-hydroxycinnamic acid derivatives and their use in cosmetic or dermatological compositions
Applicant/Assignee:
Application No.: 11/594440 Filing Date: 08/Nov/2006
Abstract:The invention relates to the use of para-coumaric acid or para-hydroxycinnamic acid derivatives in cosmetic or dermatological compositions, specifically to the use of at least one compound derived from para-coumaric acid having a general formula (I) below: in which, especially, Z represents an oxygen or an -NH- group
X and Y are identical and each represent a CH or CH2 group, as an active principle with depigmenting, free-radical-scavenging and/or antiinflammatory activity. The invention also relates to the use of the above compounds for cosmetic care or for the preparation of a pharmaceutical composition, especially for depigmenting an area of skin, having antiradical and/or antiinflammatory activity.
Priority: FR20050011364 Applic. Date: 2005-11-08
Inventor: OKOMBI SABRINA [FR]; RIVAL DELPHINE [FR]; BOUMENDJEL AHCENE [FR]; MARIOTTE ANNE-MARIE [FR]; PERRIER ERIC [FR]
Application No.: US20070183998A1 Published: 09/Aug/2007Title: Cosmetic composition
Applicant/Assignee: L'OREAL
Application No.: 11/636527 Filing Date: 11/Dec/2006
Abstract:The present invention relates a cosmetic composition comprising: at least one pigment comprising: an elongated core, a red organic colorant coating at least partially the core, and at least one binder between the core and the organic colorant.
Priority: US20050754196P Applic. Date: 2005-12-28
Inventor: SUZUKI TAKAHIRO [JP]; KANI TOSHIYUKI [JP]; OKAMOTO MARIKO [JP]
Application No.: US20070184017A1 Published: 09/Aug/2007Title: Anti-aging treatment using copper and zinc compositions
Applicant/Assignee:
Application No.: 11/452642 Filing Date: 14/Jun/2006
Abstract:Composition and methods for alleviating or eliminating age related skin conditions by providing an effective amount of one or more copper, zinc and copper-zinc compositions are disclosed. Treatment is accomplished through the use of topical compositions containing one or more copper or zinc salts and/or copper-zinc compounds or complexes, particularly copper-zinc malonate active ingredient.
Priority: US20060764967P Applic. Date: 2006-02-03
Inventor: FARYNIARZ JOSEPH R [US]; RAMIREZ JOSE E [US]
Application No.: US20070184052A1 Published: 09/Aug/2007Title: Soluble tgf-b type III receptor fusion proteins
Applicant/Assignee:
Application No.: 10/556098 Filing Date: 07/May/2004
Abstract:Soluble fusion proteins of the TGF-beta type III receptor and novel methods for their production are disclosed herein for the first time. The fusion proteins of the invention competitively inhibit the binding of members of the TGF-beta superfamily to their cell-surface receptors. Also provided are methods for using these fusion proteins to modulate the biological activity of members of the TGF-beta superfamily under in vitro or in vivo conditions, and to prevent or treat a variety of pathophysiological conditions associated with overproduction of TGF-beta or mediated by altered signaling pathways of the inhibin/activin system.
Priority: US20030469175P Applic. Date: 2003-05-09; WO2004US14175 Applic. Date: 2004-05-07
Inventor: LIN HERBERT Y [US]; DEL RE ELISABETTA L [US]; CROWLEY WILLIAM F [US]; BABITT JODIE L [US]
Application No.: US20070184096A1 Published: 09/Aug/2007Title: Stable Therapeutic Formulations
Applicant/Assignee: ALZA CORPORATION
Application No.: 11/617639 Filing Date: 28/Dec/2006
Abstract:Compositions of and methods for formulating and delivering biologically active agent formulations having enhanced physical stability, and wherein deterioration from the presence of oxygen and/or water is minimized and/or controlled, to yield a stable formulation. The compositions of and methods for formulating and delivering biologically active agents of the present invention further facilitate their incorporation into a biocompatible coating which can be employed to coat a stratum-corneum piercing microprojection, or a plurality of stratum-corneum piercing microprojections of a delivery device, for delivery of the biocompatible coating through the skin of a subject, thus providing an effective means of delivering the biologically active agents.
Priority: US20050754948P Applic. Date: 2005-12-28
Inventor: AMERI MAHMOUD [US]; CORMIER MICHEL J [US]; SELLERS SCOTT [US]; MAA YUH-FUN [US]
Application No.: US20070184121A1 Published: 09/Aug/2007Title: Healthcare and cosmetic compositions containing nanodiamond
Applicant/Assignee:
Application No.: 11/640136 Filing Date: 14/Dec/2006
Abstract:Nanodiamonds can be included in various compositions to take advantage of the ability of nanodiamond to reduce or prevent the formation of free radicals through administering the particles to a subject. Nanodiamonds can be administered through a variety of means to a tissue area of the subject, thus reducing or preventing the formation of free radicals and reducing the signs of ageing. The nanodiamonds may be incorporated into a composition that includes a variety of components including biologically or cosmetically acceptable carriers, dispersants, and additional active ingredients.
Priority: US2004-814660 Applic. Date: 2004-03-30
Inventor: SUNG CHIEN-MIN [TW]
Application No.: US20070184124A1 Published: 09/Aug/2007Title: Skin stabilizer preparation
Applicant/Assignee:
Application No.: 11/348503 Filing Date: 07/Feb/2006
Abstract:A skin stabilizer system is provided which comprises separate compositions of a corticosteroid and sulfur. The compositions may be combined in any desired ratio by the user, and applied to the skin.
Priority:
Inventor: HARLAN STEVE [US]
Application No.: US20070184134A1 Published: 09/Aug/2007Title: Pharmaceutical and cosmetic composition against skin aging
Applicant/Assignee: INDENA S.P.A
Application No.: 11/783331 Filing Date: 09/Apr/2007
Abstract:Pharmaceutical and cosmetic compositions for the prevention of skin aging, containing phospholipid complexes of extracts of Vitis vinifera, and phospholipid complexes of standardized extract from Centella asiatica.
Priority: IT2001MI01022 Applic. Date: 2001-05-17; US2003-477703 Applic. Date: 2003-11-14; WO2002EP05147 Applic. Date: 2002-05-10
Inventor: DI PIERRO FRANCESCO [IT]
Application No.: US20070184444A1 Published: 09/Aug/2007Title: Compositions and methods for the treatment of immune related diseases
Applicant/Assignee:
Application No.: 10/567939 Filing Date: 11/Aug/2004
Abstract:The present invention relates to composition containing novel proteins and method of using those compositions for the dignosis and treatment of immune related diseases.
Priority: US20030493546P Applic. Date: 2003-08-11; WO2004US26249 Applic. Date: 2004-08-11
Inventor: ABBAS ALEXANDER [US]; CLARK HILARY [US]; OUYANG WENJUN [US]; WILLIAMS P MICKEY [US]; WOOD WILLIAM I [US]; WU THOMAS D [US]
Application No.: US20070185017A1 Published: 09/Aug/2007Title: Compositions and methods for the treatment of immune related diseases
Applicant/Assignee: GENENTECH, INC
Application No.: 10/533069 Filing Date: 28/Oct/2003
Abstract:The present invention relates to compositions containing novel proteins and methods of using those compositions for the diagnosis and treatment of immune related diseases.
Priority: US20020422472P Applic. Date: 2002-10-29; WO2003US34381 Applic. Date: 2003-10-28
Inventor: AGGARWAL SUDEEPTA [US]; CLARK HILARY [US]; GURNEY AUSTIN L [US]; SCHOENFELD JILL R [US]; WILLIAMS P M [US]; WOOD WILLIAM I [US]; WU THOMAS D [US]
Application No.: US20070185038A1 Published: 09/Aug/2007Title: Regulation of mammalian keratinous tissue using skin care actives
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/541324 Filing Date: 29/Sep/2006
Abstract:Personal care compositions comprising skin and/or hair care actives. Such compositions are useful for regulating the condition of mammalian keratinous tissue needing such treatments, particularly skin lightening. In accordance with one embodiment, there is provided a personal care composition comprising a safe and effective amount of a first active selected from the group consisting of erythritol, p-cymen-7-ol, benzyl phenylacetate, 4-(4-methoxyphenyl)butan-2-one, ethoxyquin, tannic acid, gallic acid, octadecenedioic acid, p-cymen-5-ol, methyl sulfonyl methane, an avenathramide compound, and combinations thereof.
Priority: US20050722383P Applic. Date: 2005-09-30; US20060759304P Applic. Date: 2006-01-17
Inventor: BISSETT DONALD L [US]; MILLIKIN CHERI L [US]
Application No.: US20070185069A1 Published: 09/Aug/2007Title: Anti-angiogenic activity of 2-methoxyestradiol in combination with anti-cancer agents
Applicant/Assignee:
Application No.: 11/599997 Filing Date: 14/Nov/2006
Abstract:The present invention relates generally to methods and compositions of treating disease characterized by abnormal cell proliferation and/or abnormal or undesirable angiogenesis by administering antiangiogenic agents in combination with chemotherapeutic agents. More specifically, the present invention relates to a methods and compositions of treating diseases characterized by abnormal cell proliferation and/or abnormal or undesirable angiogenesis by administering 2-methoxyestradiol, in combination with chemotherapeutic agents.
Priority: US20050736220P Applic. Date: 2005-11-14; US20060788354P Applic. Date: 2006-03-31
Inventor: PLUM STACY M [US]; STRAWN STEVEN J [US]; LAVALLEE THERESA M [US]; SIDOR CAROLYN F [US]; FOGLER WILLIAM E [US]; TRESTON ANTHONY M [US]
Application No.: US20070185071A1 Published: 09/Aug/2007Title: Histone deacetylase inhibitor and process for producing the same
Applicant/Assignee: RIKEN
Application No.: 10/561298 Filing Date: 18/Jun/2004
Abstract:HDAC inhibitors represented by formula (1) show strong inhibitory activity against various subtypes of HDACs. The compounds of the present invention find utility as pharmaceutical agents for treating or preventing diseases associated with HDAC 1, 4, and 6. The methods for producing the compounds of the present invention enable easy and simple synthesis of various types of these compounds, and are expected to contribute to the development of HDAC inhibitors having novel properties and the like.
Priority: JP20030177298 Applic. Date: 2003-06-20; WO2004JP08924 Applic. Date: 2004-06-18
Inventor: YOSHIDA MINORU [JP]; NISHINO NORIKAZU [JP]
Application No.: US20070185075A1 Published: 09/Aug/2007Title: Pyrimidine derivatives
Applicant/Assignee: PFIZER LIMITED
Application No.: 11/640071 Filing Date: 15/Dec/2006
Abstract:A compound of Formula (I): or a pharmaceutically and/or veterinarily acceptable derivative thereof, wherein R<1>, R<2>, R<3>, R<4>, R<5>, and R<8 >are as defined above.
Priority: US20050752612P Applic. Date: 2005-12-20
Inventor: BELL ANDREW S [GB]; LANE CHARLOTTE A L [GB]; MOWBRAY CHARLES E [GB]
Application No.: US20070185431A1 Published: 09/Aug/2007Title: Galvanic Current Skin Treatment
Applicant/Assignee:
Application No.: 11/670643 Filing Date: 02/Feb/2007
Abstract:The present invention relates to methods and systems for application of a substance and an electrical current to a biological tissue or surface. In one embodiment, the methods and systems include application of a substance and an electrical current to the surface or tissue such that the transport or absorption of the substance into the surface or tissue is enhanced for a period of time after the electrical current has been removed.
Priority: US20060765397P Applic. Date: 2006-02-03
Inventor: KERN DALE G [US]
Application No.: US20070185432A1 Published: 09/Aug/2007Title: ELECTROKINETIC SYSTEM AND METHOD FOR DELIVERING METHOTREXATE
Applicant/Assignee: TRANSPORT PHARMACEUTICALS, INC
Application No.: 11/538249 Filing Date: 03/Oct/2006
Abstract:The electrokinetic methotrexate delivery system includes at least one applicator having a multiplicity of non-conductive micro-needles carried on a non-conductive surface of the applicator. The opposite surface is formed of electrically conductive material for contact with an active electrode. The applicator includes a matrix containing a medicament, e.g., methotrexate, or a carrier therefor between the opposite surfaces. When the applicator is applied to the individual's skin with the micro-needles penetrating the skin, an electrical current is completed through the power source, the active electrode, methotrexate, or electrically conductive carrier therefor, the targeted treatment site, the individual's body, a ground electrode and the power supply, thereby electokinetically driving the medicament through the non-conductive micro-needles into the targeted treatment site.
Priority: US2005-228461 Applic. Date: 2005-09-19
Inventor: ETHEREDGE ROBERT W III [US]; GOLDBERG DENNIS I [US]; FRIDEN PHILLIP M [US]; PETERSEN JOHN S [US]
Application No.: US20070189977A1 Published: 16/Aug/2007Title: Spray-on formulations and methods for dermal delivery of drugs
Applicant/Assignee:
Application No.: 11/640132 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to sprayable formulations, methods of drug delivery, and resultant solidified layers for dermal delivery of a drug. The formulation can include a drug, a non-volatile solvent system, a solidifying agent, and a propellant. The formulation can have an initial viscosity suitable to be expelled out of a pressurized or manual pump container and applied onto a skin surface as a layer. When applied to the skin, the formulation can form a solidified layer after at least a portion of the propellant is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20060795091P Applic. Date: 2006-04-25; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJA [US]
Application No.: US20070189978A1 Published: 16/Aug/2007Title: Compositions and methods for dermally treating musculoskeletal pain
Applicant/Assignee:
Application No.: 11/640133 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to solidifying formulations for dermal delivery of a drug for treating musculoskeletal pain, inflammation, joint pain, etc. The formulation can include a drug selected from certain drug classes, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system having one or more volatile solvent, and a non-volatile solvent system having one or more non-volatile solvent, wherein the evaporation of at least some of the volatile solvent converts the formulation on the skin into a solidified layer and the non-volatile solvent system is capable of facilitating the topical delivery of the drug(s) at therapeutically effective rates over a sustained period of time.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20050750683P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070189984A1 Published: 16/Aug/2007Title: Agents for use on skin and/or hair containing quadruply substituted cyclohexene compounds
Applicant/Assignee: BEIERSDORF AF,
Application No.: 10/571089 Filing Date: 12/Jul/2004
Abstract:The invention relates to agents for use on skin or hair, particularly for increasing skin tanning and the synthesis of melanin in skin or hair. The invention contains, in particular, cosmetic or dermatological preparations containing quadruply substituted cyclohexene compounds. The use of the preparations leads to the induction and intensification of the tanning mechanisms of skin, the intensification of hair color and thus also to an intensification of the skin's and hair's intrinsic protection.
Priority: DE20031041654 Applic. Date: 2003-09-08; WO2004EP07656 Applic. Date: 2004-07-12
Inventor: WOLBER RAINER [DE]; SCHERNER CATHRIN [DE]; TOM DIECK KAREN [DE]; SCHLENZ KATHRIN [DE]; VIETZKE JENS-PETER [DE]
Application No.: US20070189985A1 Published: 16/Aug/2007Title: Use of a compound modifying an interleukin 5, interleukin 6 and/or interleukin 10 secretion for preparing a pharmaceutical composition for rosacea treatment
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT S.N.C
Application No.: 10/589967 Filing Date: 17/Feb/2005
Abstract:The invention relates to the use of a compound which modifies, and advantageously inhibits, the secretion of at least one interleukin chosen from the group comprising IL-5, IL-6 and IL-10, for the preparation of a pharmaceutical composition for treating rosacea.
Priority: FR20040001718 Applic. Date: 2004-02-20; WO2005FR00368 Applic. Date: 2005-02-17
Inventor: DOLFI FABRIZIO [FR]; SAFONOVA IRINA [FR]
Application No.: US20070189991A1 Published: 16/Aug/2007Title: Cosmetic compositon comprising a (Thio)urethane/ (thio)urea copolymer capable of forming at least 3 hydrogen bonds, and a method of cosmetic treatment
Applicant/Assignee:
Application No.: 11/640195 Filing Date: 18/Dec/2006
Abstract:The present application relates to cosmetic compositions comprising, in a physiologically acceptable medium, a copolymer having a (thio)urethane/(thio)urea polymer skeleton, resulting from the reaction: of a first monomer having at least two polymerizable groups, which may be identical or different, chosen from -N-C-O and -N-C-S, of a monomer (b1) having at least two polymerizable groups with a labile hydrogen, of a monomer (b2), different from monomer (b1), having at least two polymerizable groups with a labile hydrogen, with at least one of these monomers comprising at least one junction group (A), capable of forming at least 3 hydrogen bonds. The disclosure also relates to a method of cosmetic treatment of keratinous materials, comprising the application of a cosmetic composition as defined above on said materials.
Priority: FR20050053913 Applic. Date: 2005-12-16; US20050754184P Applic. Date: 2005-12-28
Inventor: MOUGIN NATHALIE [FR]; SCHULTZE XAVIER [FR]; CHODOROWSKI-KIMMES SANDRINE [FR]
Application No.: US20070190004A1 Published: 16/Aug/2007Title: Substances with a probiotic action used in deodorants
Applicant/Assignee:
Application No.: 11/522766 Filing Date: 18/Sep/2006
Abstract:A method for promoting probiotic activity on the skin comprises contacting the skin with a probiotic effective amount of a substance having a probiotic effect selected from the group consisting of a plant extract, a glycerol monoalkyl ether, and a fatty acid ester or a combination of the plant extract and the glycerol monoalkyl ether whereby the growth of desired skin microbes is promoted and the growth of undesired skin microbes is inhibited.
Priority: DE200410013694 Applic. Date: 2004-03-18; DE200410032734 Applic. Date: 2004-07-07; WO2005EP02606 Applic. Date: 2005-03-11
Inventor: BOCKMUHL DIRK [DE]; HOHNE HEIDE-MARIE [DE]; JASSOY CLAUDIA [DE]; SCHOLTYSSEK REGINE [DE]; BANOWSKI BERNHARD [DE]; WADLE ARMIN [DE]; SATTLER ANDREA [DE]; BREVES ROLAND [DE]; NIEVELER SLLKE [DE]
Application No.: US20070190013A1 Published: 16/Aug/2007Title: Film and film-forming compositions
Applicant/Assignee:
Application No.: 11/352959 Filing Date: 13/Feb/2006
Abstract:The invention provides films and film forming compositions that can be applied onto a tissue surface. The film and the film forming composition comprise at least one polycarboxylated polymer and at least one polysaccharide.
Priority:
Inventor: ZHANG YELI [US]; PURI REEMA [US]; SIUTA-CRUCE PATRICIA [US]; FOREMAN PAUL B [US]; MANEGOLD TODD [US]
Application No.: US20070190019A1 Published: 16/Aug/2007Title: Compositions and methods for topical administration
Applicant/Assignee:
Application No.: 10/562113 Filing Date: 23/Jun/2004
Abstract:Vanishing cream base compositions and vanishing cream compositions suitable for topical application of an active agent to an animal or plant comprising water, at least one alcohol, a polymeric thickening agent, a skin penetration enhancing compound, and an emulsifying agent are provided. Methods for the use and manufacture of such creams are also disclosed.
Priority: US20030480230P Applic. Date: 2003-06-23; WO2004US20037 Applic. Date: 2004-06-23
Inventor: GUO CHUNFENG [US]; CHAN THOMAS [US]
Application No.: US20070190043A1 Published: 16/Aug/2007Title: Use of a topical medicament comprising riluzole
Applicant/Assignee: BIOFRONTERA AG
Application No.: 10/550774 Filing Date: 28/Apr/2004
Abstract:The present invention relates to the use of Riluzole if needed with suitable adjuvants and additives for the production of a medicament for the treatment of diseases characterized by hyperproliferation of keratinocytes and/or T cells, in particular psoriasis and neurodermatitis as well as compositions comprising Riluzole and use thereof.
Priority: EP20030009559 Applic. Date: 2003-04-28; US20030471882P Applic. Date: 2003-05-20; WO2004EP04478 Applic. Date: 2004-04-28
Inventor: SYCH MICHAEL [DE]; GOPPELT ANDREAS [DE]
Application No.: US20070190054A1 Published: 16/Aug/2007Title: Prevention and treatment of complement-associated disorders
Applicant/Assignee:
Application No.: 11/249825 Filing Date: 12/Oct/2005
Abstract:The present invention concerns a recently discovered macrophage specific receptor, CRIg, and its use in the prevention and treatment of complement-associated disorders, including complement-associated eye conditions, such as age-related macular degeneration (AMD) and choroidal neovascularization (CNV).
Priority: US2005-159919 Applic. Date: 2005-06-22; US2004-964263 Applic. Date: 2004-10-12; US2004-767374 Applic. Date: 2004-01-29; US2004-767904 Applic. Date: 2004-01-29; US2001-953499 Applic. Date: 2001-09-14; WO2003US31207 Applic. Date: 2003-10-01; US2003-633008 Applic. Date: 2003-07-31; US2002-265542 Applic. Date: 2002-10-03; US1999-254465 Applic. Date: 1999-03-05; US1999-380138 Applic. Date: 1999-08-25; WO1999US05028 Applic. Date: 1999-03-08; WO1998US24855 Applic. Date: 1998-11-20; US19980078936P Applic. Date: 1998-03-20; US19970066364P Applic. Date: 1997-11-21; WO1998US19437 Applic. Date: 1998-09-17
Inventor: ASHKENAZI AVI [US]; HELMY KARIM Y [US]; FONG SHERMAN [US]; GODDARD AUDREY [US]; GURNEY AUSTIN L [US]; KATSCHKE KENNETH J JR [US]; LOOKEREN MENNO V [US]; WOOD WILLIAM I [US]
Application No.: US20070190124A1 Published: 16/Aug/2007Title: Two or more solidifying agent-containing compositions and methods for dermal delivery of drugs
Applicant/Assignee:
Application No.: 11/640444 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive solidifying formulations, methods of drug delivery, and solidified layers for dermal delivery of a drug. The formulation can include a drug, a solvent vehicle, and at least two solidifying agents. The solvent vehicle can include a volatile solvent system including at least one volatile solvent, and a non-volatile solvent system including at least one non-volatile solvent, wherein at least one non-volatile solvent is flux-enabling non-volatile solvent(s) capable of facilitating the delivery of the drug at therapeutically effective rates over a sustained period of time. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070190126A1 Published: 16/Aug/2007Title: Method for treating generalized and focal peripheral neuropathies
Applicant/Assignee:
Application No.: 11/705651 Filing Date: 12/Feb/2007
Abstract:A composition providing cobalamine, cobalamine subtype or cobalamine analog as an effective agent for topical or transdermal administration to alleviate pain associated with a generalized or focal peripheral neuropathic condition, such as carpal tunnel syndrome.
Priority: US20060773196P Applic. Date: 2006-02-14
Inventor: STUART DANIEL M [US]
Application No.: US20070190151A1 Published: 16/Aug/2007Title: Method of preparing dendritic drugs
Applicant/Assignee: CENTRAL MICHIGAN UNIVERSITY BOARD OF TRUSTEES
Application No.: 11/653548 Filing Date: 16/Jan/2007
Abstract:Synthetic design of drug-incorporated novel dendrimer structures for quantitatively controlled drug delivery. The dendritic drugs have better control and thus a quantitative drug release can be obtained. There are no prior art dendritic drugs that control release both sequentially and quantitatively like the dendritic drugs disclosed herein. The dendritic drugs are formed by incorporating multiple same type drug units or more than two different drug types into a dendritic cascade structure to form a dendrimer drug.
Priority: US20060761439P Applic. Date: 2006-01-24
Inventor: CHAI MINGHUI [US]; TANG SCHENGZHUANG [US]
Application No.: US20070190152A1 Published: 16/Aug/2007Title: Method for providing an active agent topically to the skin
Applicant/Assignee:
Application No.: 11/676668 Filing Date: 20/Feb/2007
Abstract:A method of providing an active agent topically to the skin is provided and includes providing a topical preparation having an internal phase and an external phase, wherein the internal phase is dispersed within the external phase. The internal phase includes at least one hydrophilic carrier, at least one hydrophilic component, and at least one active agent, and the external phase comprises a silicone matrix. The topical preparation is placed in contact with the skin of a patient such that the active agent is released from the silicone matrix topically onto the skin of the patient.
Priority: US2003-660101 Applic. Date: 2003-09-10; US2003-385213 Applic. Date: 2003-03-10; US20020363386P Applic. Date: 2002-03-11; US20030439862P Applic. Date: 2003-01-14
Inventor: BOTT RICHARD R [US]; GEBERT MARK S [US]; KLYKKEN PAAL C [US]; MAZEAUD ISABELLE [FR]; THOMAS XAVIER J [US]
Application No.: US20070190558A1 Published: 16/Aug/2007Title: Cationic Steroid Antimicrobial Compositions and Methods of Use
Applicant/Assignee:
Application No.: 11/669803 Filing Date: 31/Jan/2007
Abstract:The invention provides methods for decreasing or inhibiting herpesviridae (HV) infection or pathogenesis of a cell in vitro, ex vivo or in vivo, a symptom or pathology associated with a herpesviridae (HV) infection or pathogenesis in vitro, ex vivo or in vivo, or an adverse side effect of herpesviridae (HV) infection or pathogenesis in vitro, ex vivo or in vivo. In one embodiment, a method of the invention includes treating a subject with an invention compound (e.g., cationic steroid antimicrobial or CSA).
Priority: US20060764129P Applic. Date: 2006-02-01
Inventor: SAVAGE PAUL B [US]; LEUNG DONALD [US]
Application No.: US20070190654A1 Published: 16/Aug/2007Title: Process for qualitative and/or quantitative determination of at least one molecule present on a solid surface
Applicant/Assignee: RESEARCH INSTITUTE FOR CHROMATOGRAPHY
Application No.: 11/598676 Filing Date: 14/Nov/2006
Abstract:The invention concerns a method for qualitative and/or quantitative determination of at least one molecule present on a solid surface, in which a polysiloxane-based sorbent material is used.
Priority: FR20050011517 Applic. Date: 2005-11-14; US20050748207P Applic. Date: 2005-12-08
Inventor: SISALLI SANDRA [FR]; SANDRA PATRICK [BE]
Application No.: US20070191371A1 Published: 16/Aug/2007Title: HETEROCYCLIC MODULATORS OF PPAR
Applicant/Assignee: KALYPSYS, INC
Application No.: 11/675067 Filing Date: 14/Feb/2007
Abstract:The present invention relates to compounds and methods useful as modulators of Peroxisome Proliferator-Activated Receptors (PPARs) for treatment or prevention of disease.
Priority: US20060773289P Applic. Date: 2006-02-14
Inventor: BENNETT DENNIS A [US]; SEVERANCE DANIEL L [US]; SEMPLE J E [US]
Application No.: US20070191400A1 Published: 16/Aug/2007Title: Pharmaceutical compositions comprising anti-inflammatory quinazolinecarboxamide derivatives
Applicant/Assignee: RIMONYX PHARMACEUTICALS LTD
Application No.: 10/594081 Filing Date: 24/Mar/2005
Abstract:The present invention provides pharmaceutical compositions comprising quinazolinecarboxamide derivative, and certain novel quinazolinecarboxamide derivatives capable of inhibiting heparan sulfate-glycosaminoglycan (HS-GAGs) interactions with L-selectin, and useful in the prevention or treatment of various diseases, disorders and conditions mediated by HS-GAGs, particularly inflammatory and autoimmune diseases, viral diseases, cancer, and amyloid disorders.
Priority: US20040555667P Applic. Date: 2004-03-24; WO2005IL00336 Applic. Date: 2005-03-24
Inventor: GREGOR PAUL [IL]; HARRIS NICHOLAS [IL]; KOPPEL JURAJ [SK]; ZHUK REGINA [IL]
Application No.: US20070191405A1 Published: 16/Aug/2007Title: Bi-aryl meta-pyrimidine inhibitors of kinases
Applicant/Assignee: TARGEGEN, INC
Application No.: 11/588638 Filing Date: 26/Oct/2006
Abstract:The invention provides biaryl meta-pyrimidine compounds having the general structure (A). The pyrimidine compounds of the invention are capable of inhibiting kinases, such as members of the Jak kinase family, and various other specific receptor and non-receptor kinases.
Priority: US20050732629P Applic. Date: 2005-11-01; US20060838003P Applic. Date: 2006-08-15
Inventor: NORONHA GLENN [US]; MAK CHI C [US]; CAO JIANGUO [US]; RENICK JOEL [US]; MCPHERSON ANDREW [US]; ZENG BINQI [US]; PATHAK VED P [US]; LOHSE DANIEL L [US]; HOOD JOHN D [US]; SOLL RICHARD M [US]
Application No.: US20070191432A1 Published: 16/Aug/2007Title: Novel benzo[D][1,3]-dioxol derivatives
Applicant/Assignee: CONCERT PHARMACEUTICALS INC
Application No.: 11/704554 Filing Date: 08/Feb/2007
Abstract:The present invention relates to an isotopologue of Compound 1 substituted with deuterium at the methylene carbon of the benzodioxol ring. The isotopologues of this invention selective serotonin reuptake inhibitors (SSRIs) and possess unique biopharmaceutical and metabolic properties compared to Compound 1. They may also be used to accurately determine the concentration of Compound 1 in biological fluids and to determine metabolic patterns of Compound 1 and its isotopologues. The invention further provides compositions comprising these deuterated isotopologues and methods of treating diseases and conditions that are responsive to increased neuronal serotonin transmission, alone and in combination with additional agents.
Priority: US2006-498334 Applic. Date: 2006-07-31; US20050704073P Applic. Date: 2005-07-29
Inventor: TUNG ROGER [US]
Application No.: US20070191815A1 Published: 16/Aug/2007Title: BIOSYNCHRONOUS TRANSDERMAL DRUG DELIVERY
Applicant/Assignee: CHRONO THERAPEUTICS, INC
Application No.: 11/162517 Filing Date: 13/Sep/2005
Abstract:Systems and methods for synchronizing the administration of compounds with the human body's natural circadian rhythms and addiction rhythms to counteract symptoms when they are likely to be at their worst by using an automated and pre programmable transdermal or other drug administration system.
Priority: US20040609418P Applic. Date: 2004-09-13
Inventor: DIPIERRO GUY [US]
Application No.: US20070191827A1 Published: 16/Aug/2007Title: Electrosurgical methods and devices employing phase-controlled radiofrequency energy
Applicant/Assignee: ENDYMION MEDICAL LTD
Application No.: 11/654914 Filing Date: 17/Jan/2007
Abstract:This disclosure relates generally to electrosurgical methods and devices. In one embodiment, an electrosurgical device is provided suitable for applying phase controlled RF energy to a treatment site. The electrosurgical device comprises a multi-electrode electrosurgical probe electrically coupled to a plurality of RF generators. Also provided are methods of use of such an electrosurgical device, as well as other electrosurgical devices. The methods and devices disclosed herein find utility, for example, in the field of medicine.
Priority: US20060774167P Applic. Date: 2006-02-17; US20060759289P Applic. Date: 2006-01-17
Inventor: LISCHINSKY DANIEL [IL]; HARTH YORAM [IL]
Application No.: US20070196269A1 Published: 23/Aug/2007Title: Pharmaceutical composition
Applicant/Assignee:
Application No.: 10/581547 Filing Date: 20/Dec/2004
Abstract:The invention concerns a pharmaceutical composition comprising at least one stimulator of the immune cell functions and at least one substance inhibiting the cell proliferation and/or inducing cell death. In a preferred embodiment the stimulator of the function of the immune system and/or the immune cells are antagonists of TGF-beta selected from the group of oligonucleotides hybridizing with an area of the messenger RNA and or DNA encoding TGF-beta and the at least one substance inhibiting cell proliferation and/or inducing cell death is selected from the group of temozolomide, nitrosoureas, Vinca alkaloids, antagonists of the purine and pyrimidines bases, cytoststatic active antibiotics, caphthotecine derivatives, anti estrogens, anti-androgens and analogs of gonadotropin releasing hormon.
Priority: EP20030029367 Applic. Date: 2003-12-19; US20040541771P Applic. Date: 2004-02-05; WO2004EP53604 Applic. Date: 2004-12-20
Inventor: SCHLINGENSIEPEN KARL-HERMANN [DE]; SCHLINENSIEPEN REIMAR [DE]
Application No.: US20070196292A1 Published: 23/Aug/2007Title: Personal care composition comprising dehydroacetate salts
Applicant/Assignee:
Application No.: 11/593412 Filing Date: 06/Nov/2006
Abstract:Personal care composition comprising a dehydroacetate salt, and a dermatologically acceptable carrier, wherein the pH of said composition is about 7.0 and greater.
Priority: US20050741363P Applic. Date: 2005-11-30
Inventor: ROBINSON LARRY R [US]; ZHANG YUMO [US]
Application No.: US20070196294A1 Published: 23/Aug/2007Title: Photostable sunscreen compositions comprising dibenzoylmethane compound UV-A filters and s-triazine compounds
Applicant/Assignee: L'OREAL
Application No.: 11/702051 Filing Date: 05/Feb/2007
Abstract:Photostable sunscreen compositions containing at least one dibenzoylmethane compound UV-A screening agent and at least one particular s-triazine compound have improved effectiveness with respect to UV-A radiation.
Priority: FR20060050396 Applic. Date: 2006-02-03; US20060773662P Applic. Date: 2006-02-16
Inventor: RICHARD HERVE [FR]; CANDAU DIDIER [FR]
Application No.: US20070196296A1 Published: 23/Aug/2007Title: Personal care compositions
Applicant/Assignee:
Application No.: 11/638191 Filing Date: 13/Dec/2006
Abstract:Personal care compositions comprising an active component, use of such compositions, and methods of marketing such compositions. The personal care compositions can be applied topically, ingested orally, injected, or used as part of a regimen.
Priority: US20050749906P Applic. Date: 2005-12-13
Inventor: OSBORNE ROSEMARIE [US]; MULLINS LISA A [US]; EICKHOFF DAVID J [US]; FINLAY DEBORAH R [US]; ROBINSON LARRY R [US]
Application No.: US20070196301A1 Published: 23/Aug/2007Title: Cosmetic composition with a volumizing effect
Applicant/Assignee: L'OREAL
Application No.: 11/639235 Filing Date: 15/Dec/2006
Abstract:The present invention relates to a cosmetic composition for caring for and/or making up the skin and/or the lips, containing, in a physiologically acceptable medium, at least: one active agent comprising at least one glycol with a C4-C16 hydrocarbon-based chain and/or a hydroxylated ester resulting from the esterification of polyol and/or of C4-C16 carboxylic acid(s), and one additional agent chosen from essential oils, agents for promoting capillary circulation and temperature regulators, and mixtures thereof.
Priority: FR20050013076 Applic. Date: 2005-12-21; US20060757851P Applic. Date: 2006-01-11
Inventor: BLIN XAVIER [FR]; RICARD AUDREY [FR]
Application No.: US20070196311A1 Published: 23/Aug/2007Title: Methods and kits for topical administration of hyaluronic acid
Applicant/Assignee:
Application No.: 11/375022 Filing Date: 15/Mar/2006
Abstract:The present invention provides a method for treating the skin of a subject comprising (a) applying an HA liquid to an area of the skin, wherein the HA liquid comprises hyaluronic acid, hyaluronate, cosmetically acceptable salts of hyaluronic acid, intramolecular esters of hyaluronic acid and/or intermolecular esters of hyaluronic acid
(b) massaging a self-heating mask composition into the area of the skin for a duration sufficient to activate heat, wherein the self-heating mask composition comprises at least one silicoaluminate
(c) letting the self-heating mask composition set on the area of the skin to form a mask
(d) optionally massaging the mask into the area of the skin
(e) optionally removing the mask from the area of the skin
and thereafter (f) optionally applying another skin care product to the area of the skin. The present invention also provides a kit useful for skin treatment, wherein the kit comprises the HA liquid and the self-heating mask composition comprises at least one silicoaluminate.
Priority: US20060774549P Applic. Date: 2006-02-21; US20060776922P Applic. Date: 2006-02-28
Inventor: GROSS DENNIS F [US]
Application No.: US20070196312A1 Published: 23/Aug/2007Title: Methods and kits for topical administration of hyaluronic acid
Applicant/Assignee:
Application No.: 11/375023 Filing Date: 15/Mar/2006
Abstract:The present invention provides a method for treating the skin of a subject comprising (a) applying an HA liquid to an area of the skin, wherein the HA liquid comprises hyaluronic acid, hyaluronate, cosmetically acceptable salts of hyaluronic acid, intramolecular esters of hyaluronic acid and/or intermolecular esters of hyaluronic acid
(b) massaging a self-heating mask composition into the area of the skin for a duration sufficient to activate heat, wherein the self-heating mask composition comprises at least one silicoaluminate
(c) letting the self-heating mask composition set on the area of the skin to form a mask
(d) optionally massaging the mask into the area of the skin
(e) optionally removing the mask from the area of the skin
and thereafter (f) optionally applying another skin care product to the area of the skin. The present invention also provides a kit useful for skin treatment, wherein the kit comprises the HA liquid and the self-heating mask composition comprises at least one silicoaluminate.
Priority: US20060774549P Applic. Date: 2006-02-21; US20060776922P Applic. Date: 2006-02-28
Inventor: GROSS DENNIS F [US]
Application No.: US20070196313A1 Published: 23/Aug/2007Title: Cleansing Compositions Containing Film
Applicant/Assignee:
Application No.: 11/465525 Filing Date: 18/Aug/2006
Abstract:A composition comprising a cleanser base and a plurality of film pieces, wherein the composition has a moisture content of about 22% or less. Also, a method of making a composition, comprising the steps of combining pieces of film with a cleansing material to make a cleansing mixture, and forming the mixture into a product of desired shape and size. Also, A method of delivering an active material during cleansing, comprising cleansing with water and a composition, wherein the composition comprises a plurality of film pieces, said film pieces comprising an active material and a polymer selected from water-soluble polymers, water-dispersible polymers, and combinations thereof.
Priority: US20050709402P Applic. Date: 2005-08-18
Inventor: SCALA DIANA [US]; VU LIEM [US]; BOYD THOMAS J [US]; HOURIGAN REGINA [US]; IBRAHIM SAYED [US]; HASKEL ARIEL [US]
Application No.: US20070196318A1 Published: 23/Aug/2007Title: Cosmetic herbal compositions
Applicant/Assignee:
Application No.: 11/361060 Filing Date: 22/Feb/2006
Abstract:Herbal cosmetic skin care compositions formulated to combat conditions associated with oxidative stress are provided. The compositions contain effective amounts of one of several active agents, including an herbal agent derived from one or more of the plant species, as well as cosmetically acceptable carriers. Other agents that may be included are proteins, peptides, anti-inflammatory agents, and/or vasodilators. These cosmetic compositions find use in improving the appearance of aged or damaged skin.
Priority:
Inventor: MARINI JAN L [US]
Application No.: US20070196324A1 Published: 23/Aug/2007Title: Cellulite skin treatment methods and compositions
Applicant/Assignee:
Application No.: 11/701030 Filing Date: 31/Jan/2007
Abstract:Methods for treating cellulite-affected areas on a human body include applying, to affected skin areas, while dry, a skin scrub that includes certain oils, menthone glycerin acetal, and certain organic extracts, then removing the scrub, moistening the affected areas, and applying a skin cream that includes caffeine, certain organic extracts and oils, and menthone glycerin acetal.
Priority: US20060764740P Applic. Date: 2006-02-01
Inventor: KEEFE CANDACE R [US]; ARTH MICHELLE [US]; ABBRUZZESE ANTOANETA [US]; BOTTIGLIERI PIERRE [CH]
Application No.: US20070196325A1 Published: 23/Aug/2007Title: Compositions and methods for dermally treating infections
Applicant/Assignee:
Application No.: 11/640101 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to solidifying adhesive formulations, methods of drug delivery, and solidified layers for dermal delivery of a drug which can treat various skin infections, such as fungal, bacterial, and/or viral skin infections. The formulation can include an anti-infective drug, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system including at least one volatile solvent, and a non-volatile solvent system including at least one non-volatile solvent. The non-volatile solvent system can facilitate the delivery of the drug at therapeutically effective rates for sustained period of time. The non-volatile solvent system can also act as a plasticizer for the solidifying agent. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20040577536P Applic. Date: 2004-06-07; US20050750637P Applic. Date: 2005-12-14; US20050750522P Applic. Date: 2005-12-14; US20050750465P Applic. Date: 2005-12-14
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196353A1 Published: 23/Aug/2007Title: Method for reducing allergenicity in indoor spaces
Applicant/Assignee:
Application No.: 11/239473 Filing Date: 30/Sep/2005
Abstract:According to this invention, allergenicity in an indoor space is reduced by denaturing allergens in allergen reservoirs that are capable of producing respiratory or skin reactions and physically removing the allergens from the allergen reservoirs in the indoor space. The allergen reservoirs may also be treated with pesticides and fungicides/fungistats to prevent reinfestation of house dust mites, molds and cockroaches.
Priority: US2002-153612 Applic. Date: 2002-05-24; US20010293183P Applic. Date: 2001-05-25
Inventor: PAYTON HUGH W [US]
Application No.: US20070196378A1 Published: 23/Aug/2007Title: Hyphae-Specific Cell Wall Proteins Of Candida
Applicant/Assignee: FRAUNHOFER-GESELLSCHAFT ZUR FORDERUNG DER ANGEWANDTEN FORSCHUNG E.V
Application No.: 10/593213 Filing Date: 15/Mar/2005
Abstract:Nucleic acids that code a cell wall protein required for the hyphal development of Candida
fragments of the nucleic acids
vectors containing the nucleic acids or nucleic acid fragments
host cells containing the vectors
cell wall proteins coded by the nucleic acids
antibodies directed against the proteins
methods for producing the cell wall proteins
methods for characterizing and/or for detecting the hyphal stage of Candida
methods for detecting a Candida infection
methods for identifying substances having a therapeutic effect against diseases caused by Candida
diagnostic and pharmaceutical compositions containing the nucleic acid, nucleic acids fragments, vectors, host cells, proteins and/or antibodies directed against the cell wall protein
kits for conducting in-vitro indentation of the cell wall proteins, and
to the use of the nucleic acids, vectors, proteins or antibodies for diagnosing and treating Candida-caused diseases, i.e., producing diagnostic or pharmaceutical compositions.
Priority: DE200410013826 Applic. Date: 2004-03-16; WO2005EP02748 Applic. Date: 2005-03-15
Inventor: LOTZ HENRIKE [DE]; BRUNNER HERWIG [DE]; RUPP STEFFEN [DE]
Application No.: US20070196452A1 Published: 23/Aug/2007Title: Flux-enabling compositions and methods for dermal delivery of drugs
Applicant/Assignee:
Application No.: 11/640437 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive solidifying formulations, methods of drug delivery, and solidified layers for dermal delivery of a drug. The formulation can include a drug, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system comprising at least one volatile solvent, and a non-volatile solvent system comprising at least one non-volatile solvent, wherein at least one non-volatile solvent is a flux-enabling non-volatile solvent(s) capable of facilitating the delivery of the drug at therapeutically effective rates over a sustained period of time. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20050750523P Applic. Date: 2005-12-14; US20050750652P Applic. Date: 2005-12-14; US20060795091P Applic. Date: 2006-04-25; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196453A1 Published: 23/Aug/2007Title: Two or more non-volatile solvent-containing compositions and methods for dermal delivery of drugs
Applicant/Assignee:
Application No.: 11/640445 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive formulations, methods of drug delivery, and solidified layers for dermal delivery of a drug. The formulation can include a drug, a solvent vehicle, and a solidifying agent. The solvent vehicle can have a volatile solvent system including at least one volatile solvent, and a non-volatile solvent system including at least two non-volatile solvents. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196457A1 Published: 23/Aug/2007Title: Two or more volatile solvent-containing compositions and methods for dermal delivery of drugs
Applicant/Assignee:
Application No.: 11/640117 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive formulations and methods of drug delivery. The formulation can include a drug, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system including at least two volatile solvents, and a non-volatile solvent system including at least one non-volatile solvent, wherein at least one non-volatile solvent is capable of facilitating the delivery of the drug at therapeutically effective rates over a sustained period of time. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196458A1 Published: 23/Aug/2007Title: Compositions and methods for dermally treating neuropathic pain
Applicant/Assignee:
Application No.: 11/640139 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive solidifying formulations for treating neuropathic pain. The formulation can include a drug suitable for treating neuropathic pain, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system including at least one volatile solvent, and a non-volatile solvent system including at least one non-volatile solvent capable of facilitating the delivery of the drug at therapeutically effective rates over a sustained period of time. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20050750519P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196459A1 Published: 23/Aug/2007Title: Compositions and methods for treating dermatitis or psoriasis
Applicant/Assignee:
Application No.: 11/640140 Filing Date: 14/Dec/2006
Abstract:The present invention is drawn to adhesive solidifying formulations for treating skin disorders, such as dermatitis or psoriasis. The formulation can include a drug, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system including at least one volatile solvent, and a non-volatile solvent system including at least one non-volatile solvent, wherein the non-volatile solvent system is capable of facilitating the delivery of the drug at therapeutically effective rates over a sustained period of time. The formulation can have a viscosity suitable for application to a skin surface prior to evaporation of the volatile solvents system. When applied to the skin, the formulation can form a solidified layer after at least a portion of the volatile solvent system is evaporated.
Priority: US2005-146917 Applic. Date: 2005-06-06; US20050750637P Applic. Date: 2005-12-14; US20050750524P Applic. Date: 2005-12-14; US20040577536P Applic. Date: 2004-06-07
Inventor: ZHANG JIE [US]; WARNER KEVIN S [US]; SHARMA SANJAY [US]
Application No.: US20070196490A1 Published: 23/Aug/2007Title: Method of enhancing needleless transdermal powered drug delivery
Applicant/Assignee: POWDERJECT RESEARCH LIMITED
Application No.: 11/488192 Filing Date: 18/Jul/2006
Abstract:A method is provided for enhancing the transdermal or intradermal delivery of a therapeutic agent using a needleless syringe drug delivery system. In one embodiment, the method entails first administering to a predetermined area of skin or mucosa particles comprising the therapeutic agent, a placebo and/or a permeation enhancing agent. A transdermal delivery device or occlusive dressing is then topically positioned over the area of skin or mucosa. In another embodiment, the method entails administering a formulation of particles wherein the formulation includes particles that contain a therapeutic agent and placebo particles.
Priority: US2000-489088 Applic. Date: 2000-01-21; US19990116907P Applic. Date: 1999-01-22
Inventor: KWON SUNG-YUN [US]; BURKOTH TERRY L [US]
Application No.: US20070196601A1 Published: 23/Aug/2007Title: TEXTURED FILM WITH DEEP POCKETS
Applicant/Assignee: TREDEGAR FILM PRODUCTS CORPORATION
Application No.: 11/674850 Filing Date: 14/Feb/2007
Abstract:A thermoplastic film having a first surface defining pockets, each pocket having a depth and breadth and a bottom, the bottom is preferably textured and is thinner than the thickness of the first surface. Devices made from the film include one or more of a variety of materials contained within the pockets and a second layer overlying the first surface to cover the openings of the pockets. A process of making the film is also disclosed.
Priority: US20060774456P Applic. Date: 2006-02-17
Inventor: RAY CARL DOUGLAS [US]; SEYLER RICKEY JAMES [US]; THOMAS PAUL EUGENE [US]
Application No.: US20070196663A1 Published: 23/Aug/2007Title: HIGH-YIELD ACTIVATION OF POLYMER SURFACES FOR COVALENT ATTACHMENT OF MOLECULES
Applicant/Assignee: THE TRUSTEES OF PRINCETON UNIVERSITY
Application No.: 11/677576 Filing Date: 21/Feb/2007
Abstract:Polymer surfaces coated with organometallic layers, wherein the organometallic layers and polymer surfaces have functional groups that react to bond the organometallic layer to the polymer surface with organometallic functional groups remaining unreacted for the subsequent covalent attachment of organic overlayers. Coating methods and coated articles are also disclosed.
Priority: US20060775127P Applic. Date: 2006-02-21; US20060804633P Applic. Date: 2006-06-13
Inventor: SCHWARTZ JEFFREY [US]; DENNES T J [US]
Application No.: US20070196831A1 Published: 23/Aug/2007Title: Human sample matching system
Applicant/Assignee:
Application No.: 11/360025 Filing Date: 21/Feb/2006
Abstract:Methods and apparatus for a human sample (S), analyzing the sample (S) and then determining a match with a member of the opposite sex is disclosed. In one embodiment, a customer purchases an AromaMatch(TM) Test Kit ( 14 ), which comprises a bottle of cleaning solution ( 20 ), a cotton ball ( 22 ) a sample patch ( 24 ), a sample bag ( 28 ) and a mailing envelope ( 30 ). The user ( 10 ) opens the kit ( 14 ), cleans a patch of skin somewhere on his or her body, and then applies the patch ( 24 ). After wearing the patch ( 24 ) for an appropriate time period, the patch ( 24 ) is removed, and placed in the sample bag ( 28 ). The user ( 10 ) writes his or her password on the sample bag ( 28 ), and then mails it in the return envelope ( 30 ). A laboratory analyzes the sample patch ( 24 ), and determines a set of genetic attributes (G 1 ) that are associated with the sample (S). The user ( 10 ) receives an analysis report by mail, or views the results of the analysis on a website ( 18 ), such as www.AromaMatch.com. In another embodiment, a customized perfume is manufactured that is based on biological agents that are selected to match the set of genetic attributes identified by the analysis.
Priority:
Inventor: TUCK EDWARD F [US]; HASELTON MARTIE G [US]
Application No.: US20070197501A1 Published: 23/Aug/2007Title: Use Of Chemotherapeutic Agents
Applicant/Assignee:
Application No.: 11/619823 Filing Date: 04/Jan/2007
Abstract:The use of chemotherapeutic agents for the preparation of a medicament for the topical and/or local treatment of diseases caused by bacteria and/or for prophylaxis in humans or animals.
Priority: WO2000EP13155 Applic. Date: 2000-12-22; DE19991062470 Applic. Date: 1999-12-22; US2002-168441 Applic. Date: 2002-06-21
Inventor: SCHULZ HANS-HERRMANN [DE]; SCHLIMBACH GUNTHER [DE]
Application No.: US20070197639A1 Published: 23/Aug/2007Title: Hepoxilins and modulators of ichthyin for treatment skin disorders
Applicant/Assignee: CONSORTIUM NATIONAL DE RECHERCHE EN GENOMIQUE COMPOSANTE CENTRE NATIONAL DE GENOTYPAGE (C.N.R.G.)
Application No.: 11/597840 Filing Date: 29/Nov/2006
Abstract:The present application relates to compositions and methods for treating skin disorders, dry skin, and protection of skin in inflammatory events. The present application more particularly discloses the identification of new genes and metabolic pathways involved in skin disorders, which provide novel targets and approaches for treating said disorders and for screening biologically active compounds. The present invention also provides various products and constructs, such as probes, primers, vectors, recombinant cells, which can be used to implement the above methods. The invention may be used to detect or treat various skin disorders, particularly dry and inflammatory skin disorders, in various subjects, including mammalian subjects, particularly human beings.
Priority: EP20040291387 Applic. Date: 2004-06-03; WO2005IB01763 Applic. Date: 2005-06-03
Inventor: FISCHER JUDITH [FR]
Application No.: US20070202061A1 Published: 30/Aug/2007Title: COSMETIC SKINCARE APPLICATIONS EMPLOYING MINERAL-DERIVED TUBULES FOR CONTROLLED RELEASE
Applicant/Assignee: NATURALNANO, INC
Application No.: 11/554575 Filing Date: 30/Oct/2006
Abstract:Compositions and methods pertaining to the topical treatment of skin are disclosed. The present invention relates to topical compositions for regulating the condition of skin, especially for regulating visible and/or tactile discontinuities in skin associated with skin aging, environmental affects and the like. One embodiment of the present invention relates to improving skin with compositions containing one or more non-volatile, slowly absorbed, liquid or semi-liquid organic substances (active agents) via controlled release of active agents associated with mineral-derived tubules such as halloysite nanotubules. For example, the active agents, in the form of organic substances may include vitamin compounds and glycerin, among others.
Priority: US20050731488P Applic. Date: 2005-10-31
Inventor: RIEDLINGER MICHAEL D [US]; CORKERY ROBERT W [SE]
Application No.: US20070202063A1 Published: 30/Aug/2007Title: Benefit agent containing delivery particle
Applicant/Assignee:
Application No.: 11/706675 Filing Date: 15/Feb/2007
Abstract:The present invention relates to benefit agent containing delivery particles, compositions comprising said particles, and processes for making and using the aforementioned particles and compositions. When employed in compositions, for example, cleaning or fabric care compositions, such particles increase the efficiency of benefit agent delivery, there by allowing reduced amounts of benefit agents to be employed. In addition to allowing the amount of benefit agent to be reduced, such particles allow a broad range of benefit agents to be employed.
Priority: US20060834582P Applic. Date: 2006-08-01; US20060777629P Applic. Date: 2006-02-28
Inventor: DIHORA JITEN O [US]; SANDS PEGGY D [US]; FOSSUM RENAE D [US]; YORK DAVID W [GB]; LANG MATTHEW H [US]; GUINEBRETIERE SANDRA J [US]
Application No.: US20070202067A1 Published: 30/Aug/2007Title: Stable oil-in-water and water/oil/water multiple emulsions and hair treating compositions comprising them
Applicant/Assignee:
Application No.: 11/654999 Filing Date: 18/Jan/2007
Abstract:The present invention provides an oil-in-water or water/oil/water multiple emulsion, or a mixture thereof, comprising (A) a organopolysiloxane elastomer crosslinked with polyether chains and (B) at least one thickener selected from the group of a polyacrylamide homo- or copolymer, a cellulose ether, a non-silicone cationic polymer or a thickening system comprising a mixture of from about 60% to about 67% of the thickening system of a copolymer of 2-propenoic acid with 2-propenamide, from about 27% to about 32% of the thickening system of the homopolymer of 2-methyl-1-propene and from about 5 to about 7% of the thickening system of poly(oxy-1,2-ethanediyl)-sorbitan-monododecanoate.
Priority: EP20060001090 Applic. Date: 2006-01-19
Inventor: KOLLY-HERNANDEZ MARYLINE [CH]; MULLER TIMOTHY [DE]; SPRINGOB CHRISTIAN [DE]; MONKS MONIKA [CH]; WEBER DIRK [CH]
Application No.: US20070202135A1 Published: 30/Aug/2007Title: Ionized compositions and methods of use therefore
Applicant/Assignee: ANGLESBEAUTYCARE GROUP, INC
Application No.: 11/361524 Filing Date: 24/Feb/2006
Abstract:This invention relates to methods for preparing an ionic composition suitable for use as a cosmetic product, products containing such compositions, and containers for containing and dispensing such products.
Priority:
Inventor: OUELLETTE RICHARD [US]
Application No.: US20070202197A1 Published: 30/Aug/2007Title: PAWPAW and/or peach derived composition
Applicant/Assignee: PHOENIX EAGLE PTY
Application No.: 11/713206 Filing Date: 01/Mar/2007
Abstract:There is provided a process for making a composition suitable for topical application comprising the steps of a) heating at least one fruit and/or vegetable pulp to up to a temperature in the range of about 40 DEG C. to 100 DEG C.
b) mixing between 1 and 40% w/w of a mild base with the heated fruit and/or vegetable pulp. There is also provided a fruit and/or vegetable derived composition suitable for topical application prepared by the above process. There is further provided a fruit and/or vegetable derived composition comprising at least one fruit and/or vegetable-derived pulp and a mild base, said composition having a pH in the range of about 7.5 to about 9.5.
Priority: AU20020950308 Applic. Date: 2002-07-23; US2003-521380 Applic. Date: 2003-07-22
Inventor: MCARTHUR THOMAS JAMES [US]
Application No.: US20070202203A1 Published: 30/Aug/2007Title: ANTI-AGEING COMPOSITION
Applicant/Assignee: L'OREAL
Application No.: 11/680032 Filing Date: 28/Feb/2007
Abstract:The invention relates to a composition containing, in a physiologically acceptable medium, at least: hyaluronic acid and/or one of its salts
at least one extract of soybean proteins
and at least one compound of formula (I) as described herein. This composition is useful for preventing and/or decreasing the signs of skin ageing, in particular the loss of firmness and/or of elasticity of the skin.
Priority: FR20060050706 Applic. Date: 2006-02-28; US20060785990P Applic. Date: 2006-03-27
Inventor: AMAR DAVID [FR]
Application No.: US20070202205A1 Published: 30/Aug/2007Title: Carbohydrase Inhibitors Derived From Chestnut And Use Thereof
Applicant/Assignee: CHUON CO., LTD
Application No.: 11/662638 Filing Date: 13/Sep/2005
Abstract:The present invention provides a plant-derived carbohydrase inhibitor, wherein the inhibitor is effective for preventing or alleviating diabetes, or preventing obesity, and foods, drinks, and medicines containing the same. The present invention is accomplished by use of an alpha-amylase inhibitor or an alpha-glucosidase inhibitor as a carbohydrase inhibitor that is extracted from astringent skins of a chestnut using ethanol or aqueous ethanol solution. The present invention can also be accomplished by adding the carbohydrase inhibitor to a food or medical composition as an active ingredient for delaying saccharide digestion or absorption, suppressing a rise in postprandial blood glucose levels or blood insulin levels, or preventing obesity.
Priority: JP20040265281 Applic. Date: 2004-09-13; WO2005JP17215 Applic. Date: 2005-09-13
Inventor: TSUJITA TAKAHIRO [JP]; TAKAKU TAKESHI [JP]
Application No.: US20070202206A1 Published: 30/Aug/2007Title: Morinda Citrifolia Leaf Juice And Leaf Extract Based Formulations
Applicant/Assignee:
Application No.: 11/560407 Filing Date: 16/Nov/2006
Abstract:A method and composition for inhibiting certain enzymes, where such inhibition results in various health benefits is provided. More particularly, a method and composition using one or more of the following: Noni Leaf Extract
Noni Leaf Juice
and/or Roast Leaf to inhibit the following: HMG-CoA Reductase
Phosphodiesterases (3 and 4) PDE3 and PDE4
5-Lipoxygenase (LOX) and 15-LOX
Xanthine Oxidase (XO)
Gamma Amino Butyric Acid (GABA) and the growth of the second most common human skin cancer cell line, is provided. Moreover, the foregoing enzymatic inhibitions result in: alleviating pain and inflammation
treating prostate cancers
lowering cholesterol levels
counteracting Diabetes Type II
maintaining the highest possible integrity of cellular interactions in the brain resulting in an undisturbed neural function, (i.e., neuroprotection)
ameliorating the effects of asthma and allergies
improving energy
improving insulin secretion
decreasing kidney stone accumulation
alleviating the effects of gout
minimizing convulsions related to epilepsy and other seizure disorders
and providing palliative effects to those addicted to drugs.
Priority: US20050740612P Applic. Date: 2005-11-29
Inventor: PALU AFA K [US]; ZHOU BING-NAN [US]; SU CHEN [US]; JENSEN CLAUDE J [US]; WEST BRETT [US]; STORY STEPHEN [US]
Application No.: US20070202315A1 Published: 30/Aug/2007Title: Cleansing Wipes Having A Covalently Bound Oleophilic Coating, Their Use And Processes For Their Manufacture
Applicant/Assignee: RECKITT BENCKISER (UK) LIMITED
Application No.: 11/568910 Filing Date: 13/May/2005
Abstract:A method is provided for forming an active material containing coating on a substrate. The substrate is suitably a wipe, cloth or sponge for household use, or a water-soluble household cleaning unit dose product. The method comprises the steps of: i) introducing one or more gaseous or atomised liquid and/or solid coating-forming materials which undergo chemical bond forming reactions within a plasma environment and one or more active materials which substantially do not undergo chemical bond forming reactions within a plasma environment, into an atmospheric or low pressure plasma discharge and/or an excited gas stream resulting therefrom, and ii) exposing the substrate to the resulting mixture of atomised coating-forming and at least one active material which are deposited onto the substrate surface to form a coating.
Priority: GB20040010807 Applic. Date: 2004-05-14; WO2005GB01832 Applic. Date: 2005-05-13
Inventor: DUFFIELD PAUL J [GB]; GOODWIN ANDREW J [IE]; LEADLEY STUART R [IE]; MCKECHINE MALCOLM T [GB]; O'NEILL LIAM [IE]; PUGH SIMON [GB]
Application No.: US20070202574A1 Published: 30/Aug/2007Title: Novel Saccharothrix Strain an Antibiotics Derived Therefrom, i.e. Mutactimycins and Aldgamycins
Applicant/Assignee: INSTITUT NATIONAL POLYTECHNIQUE DE TOULOUSE
Application No.: 11/597638 Filing Date: 06/Feb/2007
Abstract:The invention relates to a novel strain Saccharothrix actinomycete SA 103 deposited at CNCM on 16 Feb. 2004, number 1-3160 or a mutant strain thereof
a method and a medium for selection of said strain
and a method for the production of a broth, active concentrate and active compounds from a culture of said strain SA 103. The invention also relates to active compounds which can be obtained by the production method, i.e. novel mutatimycins and aldgamycins, pharmaceutical compositions comprising said active compounds and the use thereof in medicine and phytopharmaceuticals.
Priority: FR20040005659 Applic. Date: 2004-05-26; WO2005FR01291 Applic. Date: 2005-05-25
Inventor: ZITOUNI ABDELGHANI [DZ]; SABAOU NASSERDINE [DZ]; MATHIEU FLORENCE [FR]; LEBRIHI AHMED [FR]
Application No.: US20070203066A1 Published: 30/Aug/2007Title: Compositions and methods for inhibiting cellular proliferation
Applicant/Assignee:
Application No.: 11/636353 Filing Date: 08/Dec/2006
Abstract:Compositions and methods effective in inhibiting abnormal or undesirable cell proliferation, particularly endothelial cell proliferation and angiogenesis related to neovascularization and tumor growth are provided. The compositions comprise peptide molecules, optionally containing one or more individual peptide chains covalently linked, and optionally modified with polyethylene glycol (PEG). The methods involve administering to a human or animal the composition described herein in a dosage sufficient to inhibit cell proliferation, particularly endothelial cell proliferation. The methods are useful for treating diseases and processes mediated by undesired and uncontrolled cell proliferation, such as cancer, particularly by inhibiting angiogenesis.
Administration of the composition to a human or animal having prevascularized, metastasized tumors is useful for preventing the growth or expansion of such tumors.
Priority: US20050749276P Applic. Date: 2005-12-09
Inventor: HOLMES CHRISTOPHER P [US]; YIN QUN [US]; ZEMEDE GENET H [US]; ANGELL YVONNE M [US]; FREDERICK BRIAN T [US]; XU CAIDING [US]
Application No.: US20070203125A1 Published: 30/Aug/2007Title: Medicament Combinations for the Treatment of Respiratory Diseases
Applicant/Assignee: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Application No.: 11/675932 Filing Date: 16/Feb/2007
Abstract:The present invention relates to new medicament combinations which contain in addition to one or more, preferably one compound of general formula 1 wherein A, B, R<1>, X, n and m may have the meanings given in the claims and in the specification, at least one other active substance 2, processes for preparing them and their use as pharmaceutical compositions.
Priority: EP20060110009 Applic. Date: 2006-02-16
Inventor: KONETZKI INGO [DE]; BOUYSSOU THIERRY [DE]; PESTEL SABINE [DE]; SCHNAPP ANDREAS [DE]
Application No.: US20070203155A1 Published: 30/Aug/2007Title: Compounds And Compositions As Ppar Modulators
Applicant/Assignee: IRM LLC
Application No.: 11/597282 Filing Date: 24/May/2005
Abstract:The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPAR.
Priority: US20040574137P Applic. Date: 2004-05-24; US20050648985P Applic. Date: 2005-01-31; WO2005US18167 Applic. Date: 2005-05-24
Inventor: EPPLE ROBERT [US]; COW CHRISTOPHER [US]; XIE YONGPING [US]; WANG XING [US]; RUSSO ROSS [US]; AZIMIOARA MIHAI [US]; SAEZ ENRIQUE [US]
Application No.: US20070203240A1 Published: 30/Aug/2007Title: Personal care compositions and methods for regulating mammalian hair growth
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/711332 Filing Date: 27/Feb/2007
Abstract:Personal care composition, comprising a first ingredient selected from the group consisting of alpha-phenyl butyl nitrone (PBN), PBN doxylcyclohexane radicals, 5,5-dimethyl pyrroline N-oxide (DMPO), alpha-(4-pyridyl 1-oxide)-N-tert-butylnitrone (POBN), 2,2,6,6-tetramethylpiperidine 1-oxide, 4-hydroxytetramethylpiperidine 1-oxide, and the salts of N-(1-oxido-2,2,6,6-tetramethyl-4-piperidyl)-N,N-dimethyl-N-hydroxyethylammonium, 3,5-dibromo-4-nitrosobenzenesulfonic acid, 2-methyl-2-nitrosopropane, nitrosodisulfonic acid, alpha-(4-pyridyl-1-oxide)-N-t-butylnitrone, 3,3,5,5-tetramethylpyrroline N-oxide, and 2,4,6-tri-t-butylnitrosobenzene, spin-trapping derivatives thereof, and mixtures thereof, a second ingredient selected from the group consisting of particulate materials, panthenol, pantothenic acid derivatives, tanning actives, and mixtures thereof
and a dermatologically acceptable carrier.
Priority: US20060777068P Applic. Date: 2006-02-27
Inventor: OBLONG JOHN ERICH [US]; HULETTE BEN CHARLTON [US]
Application No.: US20070203442A1 Published: 30/Aug/2007Title: Wound Covering
Applicant/Assignee: BIO-GATE AG
Application No.: 10/585606 Filing Date: 05/Jan/2005
Abstract:The invention relates to a dressing for a wound, containing a first layer which is formed by an absorbent matrix and an antimicrobially active substance. The substance is provided on a surface of the matrix in a chemically or physically bonded matter. The surface of the matrix with the substance is coated with a hydrophilic polymer.
Priority: DE200410001594 Applic. Date: 2004-01-09; WO2005EP00048 Applic. Date: 2005-01-05
Inventor: BECHERT THORSTEN [DE]; STEINRUCKE PETER [DE]
Application No.: US20070207088A1 Published: 06/Sep/2007Title: Anti-Inflammatory Analgesic Adhesive Patch
Applicant/Assignee: TEIKOKU SEIYAKU CO, LTD
Application No.: 10/560471 Filing Date: 10/Jun/2004
Abstract:An anti-inflammatory analgesic adhesive patch which has an excellent anti-inflammatory analgesic effect and is reduced in unpleasant irritant feeling during wear. It is characterized by containing, as active ingredients, benzocaine and an ingredient having a counter-irritation effect, wherein the ingredient having a counter-irritation effect comprises one or more members selected from the group consisting of 1-menthol, d1-menthol, d1-camphor, d-camphor, methyl salicylate, glycol salicylate, peppermint oil, eucalyptus oil, capsaicin, capsicum extract, and nonylic acid vanillamide and the benzocaine is contained in an amount of 0.5 to 20 wt. %.
Priority: JP20030166774 Applic. Date: 2003-06-11; WO2004JP08097 Applic. Date: 2004-06-10
Inventor: KONISHI TATSUYA [JP]; ABE YASUKO [JP]; MACHIDA YUJI [JP]
Application No.: US20070207106A1 Published: 06/Sep/2007Title: Low molecular weight ampholytic polymers for personal care applications
Applicant/Assignee:
Application No.: 11/369044 Filing Date: 06/Mar/2006
Abstract:A cosmetically acceptable composition comprising from about 0.1 to about 10 weight percent, based on polymer solids, of a water-soluble ampholyte polymer comprising: from at least 1 to as much as 95 weight percent of the nonionic monomer acrylamide
from at least 5 to as much as 80 weight percent of the cationic monomer dimethyldiallylammonium chloride
from at least 1 to as much as 75 weight percent of the anionic monomer acrylic acid, is disclosed. The application of these polymers to a keratinous substance is also disclosed. In addition, a method of treating a keratinous substance comprising applying a cosmetically acceptable composition comprising from about 0.1 to about 10 weight percent, based on polymer solids, of an ampholyte polymer produced by the following process: (1) preparing a monomer solution containing: from at least 1 to as much as 95 weight percent of the nonionic monomer acrylamide
from at least 5 to as much as 80 weight percent of the cationic monomer dimethyldiallylammonium chloride
from at least 1 to as much as 75 weight percent of the anionic monomer acrylic acid
(2) providing a reactor and water to said reactor
(3) optionally charging said reactor with a sequestering agent, a chain transfer agent or a combination thereof
(3) purging said reactor to remove oxygen from said reactor
(4) heating the contents of said reactor
and (5) feeding said monomer solution and initiator solution into said reactor, is disclosed.
Priority:
Inventor: SABELKO JOBIAH J [US]; CRAMM JEFFREY R [US]; PATEL DAMYANTI J [US]
Application No.: US20070207107A1 Published: 06/Sep/2007Title: Silicone based emulsions for topical drug delivery
Applicant/Assignee:
Application No.: 11/699906 Filing Date: 30/Jan/2007
Abstract:A water-in-oil emulsion is provided in which the lipophilic phase of the emulsion contains a silicone fluid and an emulsifier, a hydrophilic phase, and a pharmaceutically active compound. The active pharmaceutical ingredient is dissolved or dispersed in the emulsion and is partitioned in the emulsion so that all or a portion of the amount of the chemical compound dissolved or dispersed in the emulsion is dissolved or dispersed in the aqueous phase of the emulsion. The emulsion of the invention provides increased penetration into skin of the chemical compound dissolved or dispersed in the aqueous phase.
Priority: US20060778825P Applic. Date: 2006-03-03
Inventor: WINCKLE GARETH [US]; OSBORNE DAVID W [US]; DOW GORDON J [US]
Application No.: US20070207174A1 Published: 06/Sep/2007Title: ENCAPSULATED FRAGRANCE MATERIALS AND METHODS FOR MAKING SAME
Applicant/Assignee:
Application No.: 11/278440 Filing Date: 03/Apr/2006
Abstract:The present invention is directed to novel capsules containing active materials and methods for making capsules with enhanced performance and stability. The capsules are well suited for use in personal care applications, laundry products and perfume and fragrance products.
Priority: US2005-123898 Applic. Date: 2005-05-06
Inventor: PLUYTER JOHAN G L [US]; ANASTASIOU THEODORE J [US]
Application No.: US20070207191A1 Published: 06/Sep/2007Title: PHARMACEUTICAL COMPOSITIONS AND METHODS TO ACHIEVE AND MAINTAIN A TARGETED AND STABLE COPPER STATUS AND PREVENT AND TREAT COPPER-RELATED CENTRAL NERVOUS SYSTEM DISEASES
Applicant/Assignee:
Application No.: 11/621962 Filing Date: 07/May/2007
Abstract:Compositions and methods are provided that comprise improved means to achieve and maintain a targeted level of copper status in persons in order to treat and prevent copper associated diseases.
Priority: US20060757672P Applic. Date: 2006-01-10; US20060765812P Applic. Date: 2006-02-07
Inventor: KANZER STEVE H [US]; BREWER GEORGE J [US]; STERGIS NICHOLAS [US]; ALTHAUS JOHN S [US]; BISGAIER CHARLES L [US]
Application No.: US20070207222A1 Published: 06/Sep/2007Title: COMPOSITION AND METHOD FOR TOPICAL TREATMENT OF TAR-RESPONSIVE DERMATOLOGICAL DISORDERS
Applicant/Assignee: TRISTRATA, INC
Application No.: 11/680227 Filing Date: 28/Feb/2007
Abstract:The present invention relates to a composition including a wax and a therapeutically effective amount of tar for topical treatment of a tar-responsive dermatological disorder, the composition being in liquid or light gel form when at a temperature selected from room temperature and a temperature of skin of a mammal upon application of the composition to the skin of the mammal. The invention also relates to a method of treating a tar-responsive dermatological disorder by topically applying the composition to skin of a mammal, preferably a human, that is involved with the disorder.
Priority: US20060778128P Applic. Date: 2006-03-01
Inventor: YU RUEY J [US]; VAN SCOTT EUGENE J [US]; LEE YALING [US]
Application No.: US20070207437A1 Published: 06/Sep/2007Title: Unified workstation for virtual craniofacial diagnosis, treatment planning and therapeutics
Applicant/Assignee: ORAMETRIX, INC
Application No.: 11/799390 Filing Date: 01/May/2007
Abstract:An integrated system is described in which digital image data of a patient, obtained from a variety of image sources, including CT scanner, X-Ray, 2D or 3D scanners and color photographs, are combined into a common coordinate system to create a virtual three-dimensional patient model. Software tools are provided for manipulating the virtual patient model to simulation changes in position or orientation of craniofacial structures (e.g., jaw or teeth) and simulate their affect on the appearance of the patient. The simulation (which may be pure simulations or may be so-called "morphing" type simulations) enables a comprehensive approach to planning treatment for the patient. In one embodiment, the treatment may encompass orthodontic treatment. Similarly, surgical treatment plans can be created. Data is extracted from the virtual patient model or simulations thereof for purposes of manufacture of customized therapeutic devices for any component of the craniofacial structures, e.g., orthodontic appliances.
Priority: US2003-429123 Applic. Date: 2003-05-02; US2003-340404 Applic. Date: 2003-01-09; US2000-560641 Applic. Date: 2000-04-28; US1999-452034 Applic. Date: 1999-11-30; US2001-835039 Applic. Date: 2001-04-13
Inventor: SACHDEVA ROHIT [US]; TANEJA SANJEEV [US]; SPORBERT PEER [DE]; GETTO PHILLIP [US]; MAETZEL STEPHAN [DE]; IMGRUND HANS [DE]; ABRAHAM CHARLES L [US]
Application No.: US20070207988A1 Published: 06/Sep/2007Title: TOPICAL SKIN CARE COMPOSITION
Applicant/Assignee:
Application No.: 11/747806 Filing Date: 11/May/2007
Abstract:A cream base for the topical application of skin care therapeutics and a process for making the cream base. In one embodiment, the therapeutic is tretinoin, hydroquinone and fluocinolone acetonide for the treatment of hyperpigmented skin conditions, such as melasma.
Priority: US2002-280483 Applic. Date: 2002-10-25
Inventor: PUGLIA NANCY [US]; ROTH JERRY [US]; RAMIREZ ROSARIO [US]
Application No.: US20070207999A1 Published: 06/Sep/2007Title: New Compounds
Applicant/Assignee: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Application No.: 11/675936 Filing Date: 16/Feb/2007
Abstract:The present invention encompasses compounds of general formula (1) wherein R<1 >to R<6>, X and Y are defined as in claim 1 , which are suitable for the treatment of diseases characterised by excessive or anomalous cell proliferation, as well as the use thereof for preparing a pharmaceutical composition with the above-mentioned properties.
Priority: EP20060110303 Applic. Date: 2006-02-22
Inventor: STADTMUELLER HEINZ [AT]; BAUM ANKE [AT]; BOEHMELT GUIDO [AT]; ENGELHARDT HARALD [AT]; QUANT JENS J [AT]; SOLCA FLAVIO [AT]; STEEGMAIER MARTIN [DE]; ZAHN STEPHAN K [AT]
Application No.: US20070208061A1 Published: 15/Feb/2007Title: Novel triazole derivatives as ghrelin analogue ligands of growth hormone secretagogue receptors
Applicant/Assignee: UNIVERSITY OF MONTPELLIER II LE CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE ZENTARIS GMBH UNIVERSITY OF MONTPELLIER I
Application No.: 11/502473 Filing Date: 11/Aug/2006
Abstract:The present invention provides novel triazole derivatives as ghrelin analogue ligands of growth hormone secretagogue receptors according to formula (I) that are useful in the treatment or prophylaxis of physiological and/or pathophysiological conditions in mammals, preferably humans, that are mediated by GHS receptors. The present invention further provides GHS receptor antagonists and agonists that can be used for modulation of these receptors and are useful for treating above conditions, in particular growth retardation, cachexia, short-, medium- and/or long term regulation of energy balance
short-, medium- and/or long term regulation (stimulation and/or inhibition) of food intake
adipogenesis, adiposity and/or obesity
body weight gain and/or reduction
diabetes, diabetes type I, diabetes type II, tumor cell proliferation
inflammation, inflammatory effects, gastric postoperative ileus, postoperative ileus and/or gastrectomy (ghrelin replacement therapy).
Priority: EP20050017732 Applic. Date: 2005-08-16; US20060787543P Applic. Date: 2006-03-31; US20050707941P Applic. Date: 2005-08-15
Inventor: PERRISSOUD DANIEL [DE]; MARTINEZ JEAN [FR]; MOULIN ALINE [FR]; FEHRENTZ JEAN-ALAIN [FR]; BOEGLIN DAMIEN [FR]; DEMANGE LUC [FR]
Application No.: US20070208076A1 Published: 06/Sep/2007Title: Intracorporeal medicaments for high energy phototherapeutic treatment of disease
Applicant/Assignee:
Application No.: 11/715780 Filing Date: 08/Mar/2007
Abstract:New intracorporeal radiodense medicaments and certain medical uses and methods for use of such high energy phototherapeutic medicaments for treatment of human or animal tissue are described, wherein a primary active component of such medicaments is a halogenated xanthene or halogenated xanthene derivative. The halogenated xanthenes constitute a family of potent radiosensitizers that become photoactivated upon irradiation of the treatment site with ionizing radiation. In embodiments of the present invention, such medicaments are used for treatment of a variety of conditions affecting the skin and related organs, the mouth and digestive tract and related organs, the urinary and reproductive tracts and related organs, the respiratory tract and related organs, the circulatory system and related organs, the head and neck, the endocrine and lymphoreticular systems and related organs, various other tissues, such as connective tissues and various tissue surfaces exposed during surgery, as well as various tissues exhibiting microbial or parasitic infection. In another embodiment, such medicaments are produced in various formulations including liquid, semisolid, solid or aerosol delivery vehicles.
Priority: US2001-817448 Applic. Date: 2001-03-26; US1998-216787 Applic. Date: 1998-12-21; US20000195090P Applic. Date: 2000-04-06
Inventor: DEES H C [US]; SCOTT TIMOTHY C [US]; WACHTER ERIC A [US]; FISHER WALTER G [US]; SMOLIK JOHN [US]
Application No.: US20070212306A1 Published: 13/Sep/2007Title: INTRANASAL FORMULATIONS OF INTERFERON BETA FREE OF STABILIZERS THAT ARE PROTEINS OR POLYPEPTIDES
Applicant/Assignee:
Application No.: 11/570068 Filing Date: 07/Jun/2005
Abstract:Compositions and methods are provided for intranasal delivery of interferon-beta yielding improved pharmacokinetic and pharmacodynamic results wherein the composition is free of a stabilizer that is a protein or a polypeptide. In certain aspects of the invention, the interferon-beta is delivered to the intranasal mucosa along with one or more intranasal delivery-enhancing agent(s) to yield substantially increased absorption and/or bioavailability of the interferon-beta and/or a substantially decreased time to maximal concentration of interferon-beta in a tissue of a subject as compared to controls where the interferon-beta is administered to the same intranasal site alone or formulated according to previously disclosed reports. The enhancement of intranasal delivery of interferon-beta according to the methods and compositions of the present invention allows for the effective pharmaceutical use of these agents to treat a variety of diseases and conditions in mammalian subjects.
Priority: US20040577695P Applic. Date: 2004-06-07; WO2005US19908 Applic. Date: 2005-06-07
Inventor: QUAY STEVEN C [US]; COSTANTINO HENRY R [US]
Application No.: US20070212314A1 Published: 13/Sep/2007Title: Silicone Adhesive Formulation Containing An Antiperspirant
Applicant/Assignee: DOW CORNING CORPORATION
Application No.: 11/658133 Filing Date: 27/Jul/2005
Abstract:This invention relates to a method of enhancing the adhesion of a silicone containing adhesive formulation. The method comprises mixing 1 to 99.9 wt. % of a silicone-containing adhesive formulation and 0.1 to 50 wt. % antiperspirant compound to form a composition. The composition is then applied onto a surface and allowed to cure. The invention also relates to a composition comprising 1 to 99.9 wt. % of a silicone-containing adhesive formulation and 0.1 to 50 wt. % antiperspirant salt. The resultant adhesive films are especially useful in healthcare and cosmetic applications where they inhibit perspiration and, thus, retain the adhesive strength of the adhesive.
Priority: US20040607667P Applic. Date: 2004-09-07; WO2005US27126 Applic. Date: 2005-07-27
Inventor: MURPHY KEVIN P [US]; SCHALAU GERALD K I [US]
Application No.: US20070212326A1 Published: 13/Sep/2007Title: POLYQUATERNARY ORGANOSILICON COMPOUNDS-CONTAINING COMPOSITION
Applicant/Assignee: WACKER CHEMIE AG
Application No.: 11/572535 Filing Date: 21/Jul/2005
Abstract:Polymers containing repeating organopolysiloxane blocks and including quaternary ammonium groups in the polymer chain exhibit good biocidal properties, while also exhibiting good washfastness, hydrophilicity, and softness.
Priority: DE200410036717 Applic. Date: 2004-07-29; WO2005EP07965 Applic. Date: 2005-07-21
Inventor: OCHS CHRISTIAN [DE]; SCHWAB BIRGIT [DE]
Application No.: US20070212340A1 Published: 13/Sep/2007Title: Use of bacterial phage associated lysing enzymes for the prophylactic and therapeutic treatment of various illnesses
Applicant/Assignee:
Application No.: 10/868195 Filing Date: 16/Jun/2004
Abstract:A method for the prophylactic and therapeutic treatment of bacterial infections of the skin is disclosed which comprises the treatment of an individual with an effective amount of a native or altered version of a lytic enzyme produced by a bacteria infected with a bacteriophage specific for said bacteria. The lytic enzyme is selected from a group consisting of shuffled lytic enzymes, chimeric lytic enzymes, wherein the lytic enzyme is in an environment having a pH which allows for activity of said lytic enzyme
and a carrier for delivering said lytic enzyme. Additionally, a holin protein for puncturing the membrane may be included in the composition.
Priority: US2000-560650 Applic. Date: 2000-04-28; US1999-395636 Applic. Date: 1999-09-14; US1997-962523 Applic. Date: 1997-10-31
Inventor: FISCHETTI VINCENT [US]; LOOMIS LAWRENCE [US]
Application No.: US20070212367A1 Published: 13/Sep/2007Title: Novel immunologically active peptide fragments of a proline-rich polypeptide isolated from colostral mammalian fluids for treatment of viral and non-viral diseases or diseased conditions
Applicant/Assignee:
Application No.: 11/319936 Filing Date: 13/Mar/2006
Abstract:Present invention relates to an immunologically active nonapeptide fragments of a proline-rich polypeptide isolated from mammalian colostral fluids for treatment of viral and non-viral diseases or diseased conditions, a method and a system for processing mammalian colostral fluids for isolating target peptides and proteins, a pharmaceutical formulation containing such peptides and its use for the treatment of viral diseases or diseased conditions. The product comprises proline-rich polypeptide of immuno regulatory properties. The method of processing includes, steps of passing bodies fluids, such as, mammalian colostral fluids through at least one ion exchange column such as an anionic resin and/or a cationic resin. The ion exchange column can be selected to retained large particles at a first pH level selected to remove such large particles at a maximum fluid pressure of 30 pounds per square inch (psi), preferably less than 10 psi.
Priority:
Inventor: KEECH ANDREW M [US]
Application No.: US20070212402A1 Published: 13/Sep/2007Title: Patch
Applicant/Assignee:
Application No.: 10/581827 Filing Date: 01/Dec/2004
Abstract:A patch device adapted for use in the transdermal administration to a patient of a composition including, or consisting of, a selected irritating substance, preferably dimethylformamide or DMF, the patch consisting of a layered construct adapted to be adhered to the skin of a patient and defining a depot cavity for the composition to be administered between a proximal layer and a distal layer thereof, which proximal layer is adapted in use to be located in intimate contact with the skin of the patient and which distal layer is in use disposed on the outer side thereof, the distal layer being characterised in that it is substantially impervious to the composition to be administered, and the proximal layer being characterised in that it is partially permeable to that composition, so that in use the composition may be disposed in the cavity and permeate from there through the proximal layer to be absorbed through the skin into the body of the patient, the proximal layer being further characterised in that its permeability to the irritating substance or component of such composition is less than the permeability of the patients skin to such irritating substance.
Priority: ZA20030009481 Applic. Date: 2003-12-05; WO2004IB52616 Applic. Date: 2004-12-01
Inventor: ROOVEN QAINTON V [NA]; VERMAAK SALMON J [NA]; SCHILLACK VOLKER R [ZA]; CRONIE JOHANNES [ZA]
Application No.: US20070213409A1 Published: 13/Sep/2007Title: USE OF PREPARATIONS FOR SKIN ENZYME PROTECTION
Applicant/Assignee: BEIERSDORF AG
Application No.: 11/573327 Filing Date: 24/Mar/2005
Abstract:A cosmetic preparation which comprises an active complex of panthenol, glycerol and citrate. The mass ratio of panthenol to citrate anion is from 25:1 to 5:1 and the preparation has a pH value of from 4.6 to 5.4 and an SCTE (Stratum Corneum Tryptic Enzyme) value of from 120 to 170.
Priority: WO2005EP51394 Applic. Date: 2005-03-24
Inventor: BREITENBACH UTE [DE]; SCHEPKY ANDREAS [DE]; HOLTZMANN URSULA [DE]; FILBRY ALEXANDER [DE]
Application No.: US20070218014A1 Published: 20/Sep/2007Title: Cosmetic or pharmaceutical product for topical use
Applicant/Assignee:
Application No.: 11/715418 Filing Date: 08/Mar/2007
Abstract:A cosmetic or pharmaceutical product for topical use, comprising, mixed together, the components: propellant, comprising a mixture of butane, propane, isobutane, hydroalcohol-based gel, at least one active ingredient for topical use. The components are dispensed on the body surface to be treated from a pressurized vessel. The propellant evaporates from liquid to gaseous as it exits from the pressurized vessel and upon contact with the body surface to be treated, forms gas bubbles in the gel. The bursting of these bubbles increases the kinetic energy of the gel with the active ingredient, consequently increasing the absorption rate in the layers of the skin.
Priority: IT2006PD00092 Applic. Date: 2006-03-17
Inventor: SALA STEFANO [IT]
Application No.: US20070218022A1 Published: 20/Sep/2007Title: Photostable sunscreen compositions comprising cinnamic acid ester UV-B filters, dibenzoylmethane UV-A filters and s-triazine compounds
Applicant/Assignee: L'OREAL, PARIS, FRANCE
Application No.: 11/702070 Filing Date: 05/Feb/2007
Abstract:Photostable sunscreen compositions containing at least one cinnamic acid ester UV-B screening agent, at least one dibenzoylmethane compound UV-A screening agent and at least one particular s-triazine compound have improved effectiveness with respect to UV-B radiation, while maintaining the balance in UV-A/UV-B protection during exposure to the sun.
Priority: FR20060050390 Applic. Date: 2006-02-03; US20060773659P Applic. Date: 2006-02-16
Inventor: RICHARD HERVE [FR]; CANDAU DIDIER [FR]
Application No.: US20070218026A1 Published: 20/Sep/2007Title: DNA encoding the human serine protease EOS
Applicant/Assignee:
Application No.: 10/041385 Filing Date: 08/Jan/2002
Abstract:Here we describe the molecular identification of a cDNA encoding a novel serine protease we have termed protease EOS. The deduced amino acid sequence, and it alignment with other well-characterized serine proteases indicates that it is a member of the S1 serine protease family. We have found that the protease EOS mRNA is expressed in platelets and leukocytes and more specifically eosinophils. Although this protease is abundantly expressed in ovary, retina and stomach, where it may perform important functions, its expression in platelets and certain cells of the immune system suggests that it may play roles in thrombosis and in the immune process. Enzymatically active protease EOS is amenable to further biochemical analyses for the identification of physiological substrates and specific modulators
Priority: US1999-387375 Applic. Date: 1999-08-31
Inventor: DARROW ANDREW [US]; QI JENSON [US]; ANDRADE-GORDON PATRICIA [US]
Application No.: US20070218029A1 Published: 20/Sep/2007Title: High-deposition compositions and uses thereof
Applicant/Assignee:
Application No.: 11/377057 Filing Date: 16/Mar/2006
Abstract:Provided are compositions comprising actives associated with cationically-charged delivery systems, which compositions tend to exhibit relatively high-deposition of the actives onto the skin, nails, vagina and/or hair upon application thereto, and methods of use thereof.
Priority:
Inventor: LIBRIZZI JOSEPH J [US]; COSSA ANTHONY J [US]; WALTERS RUSSEL M [US]
Application No.: US20070218114A1 Published: 20/Sep/2007Title: Soluble Strip for Oral or Topical Administration
Applicant/Assignee: PASSIONFOR LIFE HEALTHCARE LIMITED
Application No.: 11/570493 Filing Date: 13/Jun/2005
Abstract:A composition for oral administration comprising at least one active ingredient including at least one active ingredient having activity in reducing the effect of conditions of the throat or throat disorders, distributed within a soluble base material, the composition being provided as a strip for inter-oral administration, method for the preparation thereof and use thereof in alleviating throat conditions or throat disorders.
Priority: GB20040013138 Applic. Date: 2004-06-12; GB20050006018 Applic. Date: 2005-03-23; WO2005GB02330 Applic. Date: 2005-06-13
Inventor: DUGGAN ALEX [GB]; BARATOUX JEAN-LOIC [FR]
Application No.: US20070218126A1 Published: 20/Sep/2007Title: Compositions and Methods for Reducing Inflammation and Pain Associated with Acidosis
Applicant/Assignee: TAMER LABORATORIES, INC
Application No.: 11/687561 Filing Date: 16/Mar/2007
Abstract:Compositions and methods for reducing inflammation and pain associated with acidosis. One embodiment of the composition comprises a plurality of carrier particles, wherein the plurality of carrier particles hold a plurality of alkaline compounds, and wherein the alkaline compounds can be delivered to, and absorbed across, lipid membranes into the blood stream in small quantities over an extended period of time.
Priority: US20060782991P Applic. Date: 2006-03-16
Inventor: GUROL MACIT [US]; BURNS ROBERT [US]; MCNAUGHTON CANDACE [US]
Application No.: US20070218145A1 Published: 20/Sep/2007Title: METHODS AND KITS FOR POTENTIATING SKIN CARE AGENTS
Applicant/Assignee:
Application No.: 11/686690 Filing Date: 15/Mar/2007
Abstract:The present invention provides a treatment method for administering a skin care product to the skin of a subject comprising applying a self heat generation composition into an area of the skin to generate heat locally, wherein the skin care product is administered to the area of the skin before, along with, or after the application of the self heat generation composition. The self heat generation composition comprises at least one physiologically acceptable silicoaluminate, preferably sodium silicoaluminate, with the optional inclusion of at least one skin care agent, and wherein the self heat generation composition is preferably massaged into the area of the skin to promote heat generation. The present invention also provides a kit useful for skin treatment, wherein the kit comprises a skin care product and a self heat generation composition, wherein the skin care product comprises at least one skin care agent and the self heat generation composition comprises at least one physiologically acceptable silicoaluminate.
Priority: US20060783069P Applic. Date: 2006-03-17
Inventor: GROSS DENNIS F [US]
Application No.: US20070219121A1 Published: 20/Sep/2007Title: VASODILATOR PHARMACEUTICAL PREPARATION AND HEALTH FOOD COMPOSITION
Applicant/Assignee: SHIRAKO CO., LTD
Application No.: 11/752737 Filing Date: 23/May/2007
Abstract:This invention provides a novel material having a vasodilator action thereby suppressing or ameliorating various human diseases and disorders. A composition comprising, as an active ingredient, peptides obtained by hydrolyzing proteins such as proteins derived from a seaweed selected from layer, wakame, edible brown algae, sea tangle, chlorella and spirulina, proteins derived from a plant selected from soybean and sesame, proteins derived from a fish selected from bonito, mackerel, saury and horse mackerel, proteins derived from milk proteins selected from powdered skim milk and whey, proteins derived from an animal selected from cattle and swine, and collagen like proteins derived from bovine collagen, porcine skin collagen and fish scale-derived collagen is used as a pharmaceutical composition and a health food composition thereby exhibiting a vasodilator effect by which various phenomena caused by a reduction in blood stream, such as stiff neck, headache and poor circulation, can be suppressed or ameliorated.
Priority: JP20030035063 Applic. Date: 2003-02-13; US2004-771527 Applic. Date: 2004-02-05
Inventor: HAGINO HIROSHI [JP]
Application No.: US20070219128A1 Published: 20/Sep/2007Title: Medical and health-care uses of pufferfish type I collagen extract and processes for producing said extract
Applicant/Assignee: NANJING BESSON PHARMACY CO., LTD
Application No.: 10/570058 Filing Date: 27/Aug/2004
Abstract:The present invention relates to the use of pufferfish type I collagen extract as effective ingredient in the manufacture of medicaments and health-care foods for prevention and treatment of the following diseases, wherein the main chemical components and active components of the pufferfish type I collagen extract are natural pufferfish type I collagen or denatured pufferfish type I collagen extract and partial hydrolysates thereof. The present invention further relates to processes for the production of said pufferfish type I collagen extract, immunological assay methods of said extract, and uses of said extract as effective ingredient in treatment and health-care.
Priority: CN20031052848 Applic. Date: 2003-08-28; WO2004CN00996 Applic. Date: 2004-08-27
Inventor: CHEN DINGDING [CN]; GAO LIZHONG [CN]
Application No.: US20070219171A1 Published: 20/Sep/2007Title: Transdermal Pharmaceutical Spray Formulations Comprising a Vp/Va Copolymer and a Non-Aquous Vehicle
Applicant/Assignee: WATERLEAD LIMITED
Application No.: 10/576908 Filing Date: 21/Oct/2004
Abstract:Transdermal spray formulations containing a pharmaceutically active agent and methods for administering the same are provided. The formulations comprise the pharmaceutically active agent, a VP/VA copolymer and a non-aqueous vehicle. The formulations further comprise an anti-nucleating agent to prevent recrystallization of the pharmaceutically active agent and a penetration enhancer to increase the rate of drug delivery through the skin. Upon application to the skin, the present formulations dry to provide a film at the site of treatment.
Priority: IN2003MU01122 Applic. Date: 2003-10-23; WO2004GB04487 Applic. Date: 2004-10-21
Inventor: LULLA AMAR [IN]; MALHOTRA GEENA [IN]
Application No.: US20070219263A1 Published: 20/Sep/2007Title: Metronidazole/azelaic acid compositions for the treatment of rosacea
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT
Application No.: 11/723378 Filing Date: 19/Mar/2007
Abstract:Pharmaceutical compositions useful for the treatment of rosacea, in particular for the treatment of the inflammatory component thereof, contain synergistically effective amounts of each of (i) metronidazole or derivative or salt thereof and (ii) azelaic acid or derivative or salt thereof.
Priority: FR20040009879 Applic. Date: 2004-09-17; WO2005FR02281 Applic. Date: 2005-09-14
Inventor: PILGRIM WILLIAM [FR]
Application No.: US20070219275A1 Published: 20/Sep/2007Title: Use of Benzophenone Uv Filters for Preventing Tanning
Applicant/Assignee:
Application No.: 10/593521 Filing Date: 23/Mar/2005
Abstract:The invention describes the use of organic UV filters of formula (I) wherein R, and R2, 'independently from each other are hydrogen, C1-C2, alkyl, C2-C10 alkenyl, C3 C,ocycloalkyl, C3-C10cycloalkenyl, or R, and. R2 togethér with the nitrogen atom to which they are bonded can form a 5- or 6-membered ring
R3 and R4, independently from each other are C1-C20alkyl, C2 C,oalkenyl, C3-C12cycloalkyl, C3-C10cycloalkenyl, C1-C12alkoxy, C,-C20alkoxycarbonyl, C1-C,zalkylamino, C1-C12dialkylamino, aryl, heteroaryl, optionally substituted, substituents which confer solubility in water, chosen from the group consisting of a nitrile group, carboxylate, sulfonate or ammonium radicals
X is hydrogen, COOR5, CONR6R7
R5, Rs and R7, independently from each other are hydrogen, C1-C20alkyl, C2-C10alkenyl, C3-C,0cycloalkyl, C3 C10cycloalkenyl, (Y-0), -Z-aryl
Y is -(CH2)2, -(CH2)3, -(CH2)4-, -CH(CH3)-CH2
Z is -CH2 CH3i -CH2-CH,CH3, -CH2 CH2 CH2 CH3, -CH(CH3)-CH,
m is from 0 to 3
n. is from 0 to 4
o is from 1 to 20
for preventing tanning human skin, and their use in cosmetic and pharmaceutical formulations, as anti-wrinkling agents, skin-firming agents and as anti-skin lifting agents.
Priority: EP20040101375 Applic. Date: 2004-04-02; WO2005EP51325 Applic. Date: 2005-03-23
Inventor: BASCHONG WERNER [CH]
Application No.: US20070219276A1 Published: 20/Sep/2007Title: WATER-SOLUBLE ZINC IONOPHORES, ZINC CHELATORS, AND/OR ZINC COMPLEXES AND USE FOR TREATING CANCER
Applicant/Assignee: PHARMACYCLICS, INC
Application No.: 11/688789 Filing Date: 20/Mar/2007
Abstract:Disclosed herein are novel zinc ionophores, zinc chelators and/or zinc complexes with enhanced aqueous solubility. Methods of treating cancer using at least one zinc ionophore and/or zinc chelator are also disclosed. Also disclosed herein are compositions and methods for treating cancer with combination therapy using at least one texaphyrin metal complex and at least one zinc ionophore or the respective pharmaceutically acceptable derivatives or salts thereof.
Priority: US20060743588P Applic. Date: 2006-03-20
Inventor: MAGDA DARREN [US]; SESSLER JONATHAN L [US]
Application No.: US20070224130A1 Published: 27/Sep/2007Title: Tetrahydro-Naphthalene Derivatives as Glucocorticoid Receptor Modulators
Applicant/Assignee:
Application No.: 11/573301 Filing Date: 10/Aug/2005
Abstract:The present invention is directed to compounds of formula (I): wherein R represents a methyl or an ethyl group X represents N, C-H or C-CH3 when X represents C-H or C-CH3, Y represents N when X represents N, Y represents C-H and physiologically functional derivatives thereof, pharmaceutical compositions comprising the compounds, the use of the compounds for the manufacture of medicaments particularly for the treatment of inflammatory and/or allergic conditions, processes for the preparation of the compounds, and chemical intermediates in the processes for the manufacture of the compounds.
Priority: GB20040018045 Applic. Date: 2004-08-12; WO2005EP08763 Applic. Date: 2005-08-10
Inventor: EDWARDS CHRISTINE [GB]; FENTON GARRY [GB]; MACDONALD SIMON JOHN F [GB]; WEINGARTEN GORDON G [GB]; GLADWIN AMANDA R [GB]
Application No.: US20070224147A1 Published: 27/Sep/2007Title: UV-photoprotecting/sunscreen compositions comprising silane/siloxane derivatives of merocyanine sulfones
Applicant/Assignee: L'OREAL
Application No.: 11/725485 Filing Date: 20/Mar/2007
Abstract:Topically applicable cosmetic compositions useful for the UV-A photoprotection of the skin and/or hair contain thus effective amounts of at least one silane, siloxane or polysiloxane merocyanine sulfone having at least one of the structural formulae (1), (2) and (3) below:
Priority: FR20040052093 Applic. Date: 2004-09-20; WO2005FR02129 Applic. Date: 2005-08-24; US20040613967P Applic. Date: 2004-09-29
Inventor: RICHARD HERVE [FR]
Application No.: US20070224148A1 Published: 27/Sep/2007Title: Beta-(1,3)-Beta-(1,4)-Glucan as Carrier for Chemical Substances
Applicant/Assignee: SYMRISE GMBH & CO. KG
Application No.: 11/573584 Filing Date: 12/Feb/2007
Abstract:Disclosed is the use of beta-(1,3)-beta-(1,4)-glucan (a) as carrier for carrying a chemical substance through the stratum corneum into deeper layers of the skin and/or (b) for improving the penetration abilities of the chemical substance through the stratum corneum into deeper layers of the skin.
Priority: WO2004EP51793 Applic. Date: 2004-08-13
Inventor: ROEDING JOACHIM [DE]
Application No.: US20070224153A1 Published: 27/Sep/2007Title: High-deposition compositions and uses thereof
Applicant/Assignee:
Application No.: 11/377231 Filing Date: 16/Mar/2006
Abstract:Provided are compositions comprising actives associated with cationically-charged delivery systems, which compositions tend to exhibit relatively high-deposition of the actives onto the skin, nails, vagina and/or hair upon application thereto, and methods of use thereof.
Priority:
Inventor: LIBRIZZI JOSEPH J [US]; COSSA ANTHONY J [US]; WALTERS RUSSEL M [US]
Application No.: US20070224229A1 Published: 27/Sep/2007Title: Cosmetic composition comprising Seabuckthorn
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/726041 Filing Date: 20/Mar/2007
Abstract:Cosmetic compositions are provided comprising a hydrophilic extract of Seabuckthorn and a hydrophilic vitamin component. The cosmetic use of that composition is also provided.
Priority: EP20060005854 Applic. Date: 2006-03-22
Inventor: GIBBONS CLYDE [GB]; WATSON ANDREW DAVID [GB]; MORRIS SIAN [GB]
Application No.: US20070224231A1 Published: 27/Sep/2007Title: Anti Acne Skincare Composition and Skincare Article
Applicant/Assignee: RECKITT & COLMAN (OVERSEAS) LIMITED
Application No.: 11/596581 Filing Date: 11/May/2005
Abstract:There is disclosed a cleansing and moisturising composition for topical application to the skin. The composition comprises salicylic acid as active ingredient, and has the form of an emulsion comprising 70-95% by weight of an aqueous phase and 5-30% by weight of an oil phase, the salicylic acid being dissolved in the oil phase, and the composition comprising one or more moisturising agents. The composition may be incorporated into a wipe substrate for ease of application to the skin. The compositions have the combined effects of cleansing and moisturising the skin and may be used in the prophylactic or remedial treatment of acne.
Priority: GB20040010860 Applic. Date: 2004-05-15; WO2005GB01834 Applic. Date: 2005-05-11
Inventor: SCHMIDT TIMM [DE]
Application No.: US20070224261A1 Published: 27/Sep/2007Title: EUTECTIC LIQUID DRUG FORMULATION
Applicant/Assignee:
Application No.: 11/684666 Filing Date: 12/Mar/2007
Abstract:A drug formulation dosage is provided that includes an oral medication capsule inclusive of the eutectic liquid at room temperature. The eutectic liquid includes a pharmaceutically active substance that exists as a solid in pure form at room temperature along with a biologically tolerated compound that forms a eutectic liquid with the active substance so as to render the substance and the compound as the eutectic liquid. The resulting drug formulation dosage has a high degree of storage stability. Natural volatile oils represent a class of biologically tolerated compounds well suited for the formation of a eutectic liquid sealed within an oral medication capsule. Three or more component eutectics are also appreciated to be operative herein to form stable eutectic liquids with pharmaceutically active substances. A process for delivering a pharmaceutically active substance existing at room temperature in pure form as a solid as an oral dosage includes administering to a subject orally a pharmaceutically effective amount of the substance as a eutectic liquid formed with the biologically tolerated natural volatile oil. The eutectic liquid is contained within a capsule disintegrating subsequent to administration to the subject and thereby releasing the pharmaceutically active substance. A transdermal medicament delivery system is also provided that includes multiple small capsules of a drug formulation dosage as detailed above. The integrity of the capsule is compromised after exposure to subject skin through temperature, perspiration dissolution or concussion. A skin compatible adhesive matrix retains the multiple drug formulation dosage capsules in contact with subject skin so as to release the active substance into contact with subject skin.
Priority: US20060784673P Applic. Date: 2006-03-22
Inventor: DRAPER PETER [CA]
Application No.: US20070224297A1 Published: 27/Sep/2007Title: Method for increasing content of physiologically active substance in ginseng
Applicant/Assignee:
Application No.: 11/725885 Filing Date: 20/Mar/2007
Abstract:The present invention relates to a method for economically preparing ginseng extract having an increased content of physiologically active substances, comprising the steps of steaming ginseng at 95 to 100 DEG C. for 1 to 24 hours, collecting the generated vapor by cooling, and repeating the process twice, to a composition for promoting collagen synthesis, comprising the extract, and to a cosmetic product for improving skin wrinkles, comprising the composition.
Priority: KR20060025865 Applic. Date: 2006-03-21
Inventor: PARK DEOK HOON [KR]; LEE JONG SUNG [KR]; JUNG EUNSUN [KR]
Application No.: US20070225190A1 Published: 27/Sep/2007Title: Methods for modifying cellulosic polymers in ionic liquids
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/726609 Filing Date: 22/Mar/2007
Abstract:Sulfation or sulfonation of cellulose and cellulose ethers is conducted in an ionic liquid such as a quaternary ammonium salt. Detergent compositions containing the sulfated or sulfonated reaction product are suitable for fabric cleansing.
Priority: US20060786415P Applic. Date: 2006-03-27
Inventor: SCHEIBEL JEFFREY JOHN [US]; KENNEALLY COREY JAMES [US]; MENKHAUS JULIE ANN [US]; SEDDON KENNETH RICHARD [IE]; CHWALA PREZEMYSLAW [PL]
Application No.: US20070225191A1 Published: 27/Sep/2007Title: Methods for modifying bioplymers in ionic liquids
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/726629 Filing Date: 22/Mar/2007
Abstract:Sulfation or sulfonation of biopolymers such as starch, chitosan, dextrins, gums and the like is conducted in an ionic liquid such as a quaternary ammonium salt. Detergent compositions containing the sulfated or sulfonated reaction product are suitable for fabric cleansing.
Priority: US20060786191P Applic. Date: 2006-03-27
Inventor: SCHEIBEL JEFFREY JOHN [US]; MENKHAUS JULIE ANN [US]; PRICE KENNETH NATHAN [US]
Application No.: US20070225229A1 Published: 27/Sep/2007Title: N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
Applicant/Assignee: MERCK SHARP & DOHME CORP
Application No.: 11/712727 Filing Date: 01/Mar/2007
Abstract:Compounds of structural formula I are modulators of the androgen receptor (AR) in a tissue selective manner. These compounds are useful in the enhancement of weakened muscle tone and the treatment of conditions caused by androgen deficiency or which can be ameliorated by androgen administration, including osteoporosis, osteopenia, glucocorticoid-induced osteoporosis, periodontal disease, bone fracture, bone damage following bone reconstructive surgery, sarcopenia, frailty, aging skin, male hypogonadism, postmenopausal symptoms in women, atherosclerosis, hypercholesterolemia, hyperlipidemia, obesity, aplastic anemia and other hematopoietic disorders, inflammatory arthritis and joint repair, HIV-wasting, prostate cancer, benign prostatic hyperplasia (BPH), abdominal adiposity, metabolic syndrome, type II diabetes, cancer cachexia, Alzheimer's disease, muscular dystrophies,
cognitive decline, sexual dysfunction, sleep apnea, depression, premature ovarian failure, and autoimmune disease, alone or in combination with other active agents.
Priority: US2005-145490 Applic. Date: 2005-06-03; US20040577698P Applic. Date: 2004-06-07
Inventor: HANNEY BARBARA [US]; KIM YUNTAE [US]; KROUT MICHAEL R [US]; MEISSNER ROBERT S [US]; MITCHELL HELEN J [US]; MUSSELMAN JEFFREY [US]; PERKINS JAMES J [US]; WANG JIABING [US]
Application No.: US20070225234A1 Published: 27/Sep/2007Title: TOPICAL FORMULATION OF OIL-IN-WATER TYPE AS A CARRIER FOR PROVIDING A REDUCED IRRITANT EFFECT
Applicant/Assignee:
Application No.: 11/754044 Filing Date: 25/May/2007
Abstract:A topical formulation of the oil-in-water type comprising an oily material, an aqueous phase and an emulsifier, wherein the emulsifier is a galactolipid material, as a carrier for providing a reduced irritant effect of an incorporated active substance on the skin. New topical formulations are also described.
Priority: SE19980000730 Applic. Date: 1998-03-06; US2003-361830 Applic. Date: 2003-02-11; US2000-623601 Applic. Date: 2000-09-05; WO1999SE00348 Applic. Date: 1999-03-08
Inventor: CARLSSON ANDERS [SE]; EK JENNY [SE]; HERSLOF BENGT [SE]; KARLSSON EWA [SE]; NILSSON GORAN [SE]
Application No.: US20070225243A1 Published: 27/Sep/2007Title: Treatment of cancer using cytokine-expressing polynucleotides and compositions therefor
Applicant/Assignee: VICAL INCORPORATED
Application No.: 11/709868 Filing Date: 23/Feb/2007
Abstract:The present invention provides a pharmaceutical composition, comprising a non-infectious, non-integrating polynucleotide construct comprising a polynucleotide encoding an interferon omega and one or more cationic compounds. The present invention also provides methods of treating cancer in a mammal, comprising administering into a tissue of the mammal a non-infectious, non-integrating polynucleotide construct comprising a polynucleotide encoding a cytokine. In addition, the present invention also relates to the methodology for selective transfection of malignant cells with polynucleotides expressing therapeutic or prophylactic molecules in intra-cavity tumor bearing mammals. More specifically, the present invention provides a methodology for the suppression of an intra-cavity dissemination of malignant cells, such as intraperitoneal dissemination.
Furthermore, the invention relates to compositions and methods to deliver polynucleotides encoding polypeptides to vertebrate cells in vivo, where the composition comprises an aqueous solution of sodium phosphate.
Priority: US2000-557907 Applic. Date: 2000-04-21; US1998-196313 Applic. Date: 1998-11-20; US19970067087P Applic. Date: 1997-11-20; US19980079914P Applic. Date: 1998-03-30; US19980100820P Applic. Date: 1998-09-15
Inventor: HORTON HOLLY [US]; PARKER SUEZANNE [US]; MANTHORPE MARSTON [US]; FELGNER PHILIP L [US]; HARTIKKA JUKKA [US]
Application No.: US20070225245A1 Published: 27/Sep/2007Title: Viral vector driven mutant bacterial cytosine deaminase gene and uses thereof
Applicant/Assignee:
Application No.: 11/796574 Filing Date: 27/Apr/2007
Abstract:The instant invention has developed viral vectors encoding a mutant bacterial cytosine deaminase (bCD) gene, which have a higher affinity for cytosine than wild type bCD (bCDwt). The purpose of the present invention was to evaluate cytotoxicity in vitro and therapeutic efficacy in vivo of these vectors in combination with the prodrug 5-FC and ionizing radiation against human glioma. The present study demonstrates that infection with the viral vector expressing the mutant cytosine deaminase gene resulted in increased 5-FC-mediated cell killing, compared with vectors expressing the wild-type gene. Furthermore, a significant increase in cytotoxicity following infection with viral vector expressing the mutant cytosine deaminase gene and radiation treatment of glioma cells in vitro was demonstrated as compared to infection with viral vector expressing the wild-type gene. Animal studies showed significant inhibition of subcutaneous or intracranial tumor growth of D54MG glioma xenografts by the combination of AdbCD-D314A/5-FC with ionizing radiation as compared with either agent alone, and with AdbCDwt/5-FC plus radiation. These data indicate that combined treatment with this mutant enzyme/prodrug therapy and radiotherapy provides a promising approach for cancer therapy.
Priority: US2004-795551 Applic. Date: 2004-03-08; US2002-304436 Applic. Date: 2002-11-26; US2000-706190 Applic. Date: 2000-11-03; US1999-408055 Applic. Date: 1999-09-29; US19980102391P Applic. Date: 1998-09-29
Inventor: BUCHSBAUM DONALD J [US]; GILLESPIE G Y [US]; MARKERT JAMES M [US]; KALIBEROV SERGEY A [US]
Application No.: US20070225301A1 Published: 27/Sep/2007Title: TREATMENT OF ACNE AND OTHER DISEASES
Applicant/Assignee: ASTION INFLAMMATION APS
Application No.: 11/673677 Filing Date: 12/Feb/2007
Abstract:The invention relates to compounds for the treatment of dermatological diseases where inflammation, matrix metalloproteinases (MMPs) and peroxisome proliferator-activated receptors (PPARs) play a role in mediating the disease, such as the treatment of acne with Pemirolast or a closely related compound thereof.
Priority: US20060772527P Applic. Date: 2006-02-13
Inventor: WEIDNER MORTEN S [DK]
Application No.: US20070225360A1 Published: 27/Sep/2007Title: Anti-aging composition containing phloretin
Applicant/Assignee: L'OREAL
Application No.: 11/726176 Filing Date: 20/Mar/2007
Abstract:An anti-aging composition containing: (a) at least one first active ingredient chosen from phloretin and its derivatives
(b) at least one second active ingredient chosen from cinnamic acid, resveratrol, retinol, ascorbic acid, tocopherol, and their derivatives
and (c) at least one non-aqueous organic solvent, with the proviso that if the composition contains ascorbic acid, water is present as a co-solvent.
Priority: US20060784571P Applic. Date: 2006-03-22
Inventor: PINNELL SHELDON R [US]; ZIELINSKI JAN [US]; HANSENNE ISABELLE [US]
Application No.: US20070225377A1 Published: 27/Sep/2007Title: Bridged Ring Structures as Pharmaceutical Agents
Applicant/Assignee: X-CEPTOR THERAPEUTICS, INC
Application No.: 10/576228 Filing Date: 13/Oct/2004
Abstract:The present invention is directed to 1alpha,25-dihydroxyvitamin D3 mimics which modulate the vitamin D receptor (VDR). The invention is further directed to pharmaceutical compositions and methods for the treatment, prevention or amelioration of one or more symptoms of disease or disorder related to the activity of the vitamin D receptor using an effective amount of a compound of formula (I).
Priority: US20030511457P Applic. Date: 2003-10-14; WO2004US33666 Applic. Date: 2004-10-13
Inventor: FLATT BRENTON T [US]; MARTIN RICHARD [US]; MOHAN RAJU [US]; MURPHY BRETT [US]
Application No.: US20070225379A1 Published: 27/Sep/2007Title: TRANSDERMAL DELIVERY OF SYSTEMICALLY ACTIVE CENTRAL NERVOUS SYSTEM DRUGS
Applicant/Assignee:
Application No.: 11/755923 Filing Date: 31/May/2007
Abstract:The invention relates to a transdermal or transmucosal non-occlusive, semi-solid pharmaceutical formulation that includes at least one systemically active agent that acts on the Central Nervous System (CNS) of a mammal
and a permeation enhancing solvent system present in an amount sufficient to solubilize the at least one active ingredient. The permeation enhancing solvent system includes a pharmaceutically acceptable monoalkyl ether of diethylene glycol
a pharmaceutically acceptable glycol
preferably also a fatty alcohol and or a fatty acid
and a mixture of a C2 to C4 alcohol and water so that the permeation enhancing solvent system (a) inhibits crystallization of the at least one active ingredient on a skin or mucosal surface of a mammal, (b) reduces or prevents transfer of the formulation to clothing or to another being, (c) modulates biodistribution of the at least one active agent within different layers of skin, (d) facilitates absorption of the at least one active agent by a skin or a mucosal surface of a mammal, or (e) provides a combination of one or more of (a) through (d).
Priority: US2006-371042 Applic. Date: 2006-03-07; WO2004EP11175 Applic. Date: 2004-10-06; US2006-634005 Applic. Date: 2006-12-04; US2003-343570 Applic. Date: 2003-05-19; WO2001EP09007 Applic. Date: 2001-08-03; US20030510613P Applic. Date: 2003-10-10
Inventor: CARRARA DARIO NORBERTO R [CH]; GRENIER ARNAUD [FR]; ALBERTI IGNO [FR]; HENRY LAETITIA [FR]; DECAUDIN CELINE [FR]
Application No.: US20070226916A1 Published: 04/Oct/2007Title: COMPOSITION CONTAINING AT LEAST ONE HYDROXY ACID, AT LEAST ONE MONO- OR DISACCHARIDE AND AT LEAST ONE CERAMIDE, AND METHODS
Applicant/Assignee: L'OREAL
Application No.: 11/686968 Filing Date: 16/Mar/2007
Abstract:Composition which, in a preferred embodiment, contains, in a cosmetically acceptable medium, at least one monosaccharide and/or disaccharide, at least one alpha-hydroxy acid, and at least one ceramide compound. Uses include topical application for the treatment of keratinous substances, in particular keratinous fibres, especially the hair.
Priority: FR20060051187 Applic. Date: 2006-04-04; US20060796861P Applic. Date: 2006-05-03
Inventor: MELLUL MYRIAM [FR]; STURLA JEAN-MICHEL [FR]
Application No.: US20070231255A1 Published: 04/Oct/2007Title: Method for the Treatment of Mammalian Skin Tissues Via Pulse Irradiation in the Presence of a Photoactive Compound
Applicant/Assignee: DERMA LASER INC
Application No.: 11/660088 Filing Date: 15/Aug/2005
Abstract:A method of treating mammalian skin tissues for causing a predetermined physiological change in the mammalian skin tissues. A treatment composition of matter is applied onto the mammalian skin. The mammalian skin is irradiated with a first pulse having a power density above an activation threshold power density and with a second pulse. The first pulse is emitted for a duration of from about 1 fem-tosecond to about 1 hour, and the first pulse is separated from the second pulse by an inter-pulse interval of from about 1 microsecond to about 10 seconds. The treatment composition of matter includes a photoreactive substance and is applied in an amount sufficient to cause physiological changes within the mammalian skin tissue upon the mammalian skin tissue being irradiated.
Priority: US20040601117P Applic. Date: 2004-08-13; WO2005CA01243 Applic. Date: 2005-08-15
Inventor: BAROLET DANIEL [CA]; BOUCHER ANNIE [CA]
Application No.: US20070231285A1 Published: 04/Oct/2007Title: Method for regulating the appearance of skin containing combination of skin care actives
Applicant/Assignee:
Application No.: 11/711778 Filing Date: 28/Feb/2007
Abstract:A method for regulating the appearance of skin comprising topically applying to said skin a composition comprising: (a) a cosmetically or pharmaceutically acceptable carrier and about 0.05% to about 5% of an extract comprising a low molecular weight hydrolysable tannins, and mixtures thereof
(b) an effective amount of at least one additional skin care active ingredient selected from the group consisting of ant-acne actives, retinoids, ant-cellulite agents, antimicrobial actives, antifungal agents, vitamins, anti-inflammatory agents, tanning agents, allantoin, glucosamine, phytantriol, hydroxyacids, niacinamide, phytosterols, sunscreens and mixtures thereof.
Priority: US2004-803160 Applic. Date: 2004-03-18; US2002-120156 Applic. Date: 2002-04-11; US2003-616299 Applic. Date: 2003-07-10; US20030455396P Applic. Date: 2003-03-18; US20020395612P Applic. Date: 2002-07-15
Inventor: CHAUDHURI RATAN K [US]
Application No.: US20070231287A1 Published: 04/Oct/2007Title: COSMETIC COMPOSITION FOR CARE AND/OR TREATMENT AND/OR MAKEUP OF THE EMULSION TYPE STRUCTURED WITH SILICONE POLYMERS
Applicant/Assignee: L'OREAL
Application No.: 11/684703 Filing Date: 12/Mar/2007
Abstract:Cosmetic emulsion for care and/or makeup, comprising an aqueous phase and a liquid fatty phase dispersed one within the other, said liquid fatty phase comprising at least one silicone oil and being structured with at least one gelling polymer (homopolymer or copolymer) with a weight-average molecular mass ranging from 500 to 500,000, containing at least one moiety comprising: at least one polyorganosiloxane group, composed of 1 to 1000 organosiloxane units in the chain of the moiety or in the form of a graft, and at least two groups capable of establishing hydrogen interactions chosen from among the ester, amide, sulfonamide, carbamate, thiocarbamate, urea, thiourea, oxamido, guanidino, biguanidino groups, and combinations thereof, on condition that at least one of the groups is other than an ester group, the polymer being solid at room temperature and soluble in the liquid fatty phase at a temperature of 25 to 250 DEG C., the aqueous phase, the liquid fatty phase and the gelling polymer forming a physiologically acceptable medium.
Priority: US2002-166648 Applic. Date: 2002-06-12
Inventor: LU SHAOXIANG [US]
Application No.: US20070231289A1 Published: 04/Oct/2007Title: Use of ester quats in compositions as sand-repellent substances
Applicant/Assignee: GOLDSCHMIDT GMBH
Application No.: 11/732450 Filing Date: 03/Apr/2007
Abstract:The use of ester quats in compositions, the ester quats producing a sand-repellent action for the compositions, comprising cosmetic compositions, and the use of these cosmetic compositions having a sand-repellent action for topical application, for example for protection of the skin against ultraviolet radiation are provided. The present application in particular relates to the use of at least one ester quat based on alkanolamines in compositions, the ester quats producing a sand-repellent action for the compositions, and the acyl component of the ester quats being derived from (a) monocarboxylic acids, (b) dicarboxylic acids, (c) tricarboxylic acids, or their mixtures.
Priority: DE200610015753 Applic. Date: 2006-04-04
Inventor: GRUNING BURGHARD [DE]; JENNI KLAUS [DE]; MATHIAK RALF [DE]; MEYER JURGEN [DE]; WEITEMEYER CHRISTIAN [DE]
Application No.: US20070231314A1 Published: 04/Oct/2007Title: Polypeptides and compositions derived from the horny layer of the epidermis and its use
Applicant/Assignee: L'OREAL
Application No.: 11/546842 Filing Date: 11/Oct/2006
Abstract:The present invention relates to a cosmetic or pharmaceutical composition comprising, in a physiologically acceptable medium, a purified natural or synthetic epidermis-specific polypeptide which is involved in horny layer cell cohesion. The invention also relates to a cosmetic or pharmaceutical composition comprising a mixture of polypeptides derived from the proteolysis of the purified polypeptide of the present invention. The present invention further relates to a method for strengthening horny layer cell cohesion which comprises applying the cosmetic or pharmaceutical composition of the present invention to the skin. Finally, the present invention relates to a method for reducing horny layer cell cohesion, and thereby promoting exfoliation, wherein said method comprises applying to the skin a cosmetic or pharmaceutical composition comprising an effective amount of at least one protease active on the polypeptide of the present invention.
Priority: FR19970003899 Applic. Date: 1997-03-28; FR19970011317 Applic. Date: 1997-09-11; US2003-677865 Applic. Date: 2003-10-03; US1999-381656 Applic. Date: 1999-12-29; WO1998FR00636 Applic. Date: 1998-03-27
Inventor: SERRE GUY BRUNO R [FR]; SIMON MICHEL [FR]; WEBER-VIVAT MARINA [FR]
Application No.: US20070231356A1 Published: 04/Oct/2007Title: THIN FILM STRIPS
Applicant/Assignee:
Application No.: 11/758821 Filing Date: 06/Jun/2007
Abstract:A method of forming a thin film strip and thin film strips formed thereby where the method comprises coating a liner substrate with a wet slurry of film forming ingredients and other components and drying the wet slurry in a drying apparatus to form a film, measuring the moisture content of the film either during of upon exit from the drying apparatus, and storing the film in a minimal moisture loss environment during a curing process.
Priority: US2004-922502 Applic. Date: 2004-08-20; US2002-226451 Applic. Date: 2002-08-23
Inventor: BERRY CRAIG J [US]; KLAUSER WALTER [US]
Application No.: US20070231377A1 Published: 04/Oct/2007Title: COMPOSITIONS FOR PROMOTING HAIR GROWTH
Applicant/Assignee: NOVUS INTERNATIONAL INC
Application No.: 11/692569 Filing Date: 28/Mar/2007
Abstract:The present invention provides compositions and methods for treating hair loss, nail brittleness and skin conditions, and for promoting or enhancing hair growth. The composition generally includes at least one methionine analog or derivative. The invention further provides structured fluid delivery systems comprising the compositions of the invention.
Priority: US20060786754P Applic. Date: 2006-03-28
Inventor: ABOU-NEMEH IBRAHIM [US]
Application No.: US20070231418A1 Published: 04/Oct/2007Title: EMULSION CONTAINING A PLANT EXTRACT, METHOD FOR PRODUCING SAID EMULSION AND FOR OBTAINING SAID PLANT EXTRACT
Applicant/Assignee: BIRKEN GMBH
Application No.: 11/748304 Filing Date: 14/May/2007
Abstract:The invention provides a continuous process for obtaining triterpenes from plants and/or their components. The process can include continuously washing at least one of plant and plant parts in counter-current at 20 DEG C. to 70 DEG C. with a solvent in which the triterpenes are not soluble or only slightly soluble and continuously extracting triterpenes from the washed plant part or parts with a solvent under an increased pressure and an elevated temperature relative to the washing pressure and temperature in counter-current to form a triterpene containing solution where the plant parts are conveyed in counter-current to the solvent flow, on the basis of their different density in a pressure-tight and heatable tube and are discharged at an end of the tube opposite to the solvent discharge.
The process can also include the steps of continuously cooling and depressurizing the triterpene containing solution, where triterpene crystallizes out of the solvent, filtering the triterpene crystals from the solvent at room temperature and washing the triterpene crystals in fresh solvent.
Priority: DE20001015353 Applic. Date: 2000-03-28; DE20001056902 Applic. Date: 2000-11-16; US2002-239929 Applic. Date: 2002-09-26; WO2001EP03417 Applic. Date: 2001-03-26
Inventor: SCHEFFLER ARMIN [DE]
Application No.: US20070232564A1 Published: 04/Oct/2007Title: Fish-Origin Chondroitin Sulfate/Dermatan Sulfate Hybrid Chain
Applicant/Assignee: MARUHA CORPORATION
Application No.: 11/587789 Filing Date: 25/Apr/2005
Abstract:It is intended to provide a novel chondroitin sulfate/dermatan sulfate hybrid chain having biding activity toward a variety of growth factors, neurite outgrowth-promoting activity, and anticoagulant activity and to provide a composition for neurological disease treatment. The novel chondroitin sulfate/dermatan sulfate hybrid chain was separated and purified from the bodies of fishes other than bony fishes. When shark skin is used, the hybrid chain comprises a disaccharide GlcUA(2S)-GalNAc(4S) and has an average molecular weight of 65 to 75 kDa, and the degree of sulfation per disaccharide molecule falls within the range of 0.7 or more to less than 1.20. The hybrid chain is capable of binding to a variety of growth factors and further possesses neurite outgrowth-promoting activity and anticoagulant activity.
Priority: JP20040308584 Applic. Date: 2004-10-22; US20040565511P Applic. Date: 2004-04-27; WO2005JP08326 Applic. Date: 2005-04-25
Inventor: SUGAHARA KAZUYUKI [JP]
Application No.: US20070232565A1 Published: 04/Oct/2007Title: NOVEL POLYSACCHARIDES AND OLIGOSACCHARIDES
Applicant/Assignee: MARUHA CORPORATION
Application No.: 11/694075 Filing Date: 30/Mar/2007
Abstract:Polysaccharides and oligosaccharides having activity of binding to different proliferation factors and neurite outgrowth-promoting activity and compositions for neurological disease treatment, compositions for inflammatory disease treatment, or compositions for wound treatment, which comprise such polysaccharides and oligosaccharides, are provided. Chondroitin sulfate/dermatan sulfate hybrid chains, chondroitin sulfate C, and oligosaccharides derived from either thereof are provided.
Priority: JP20060098722 Applic. Date: 2006-03-31; JP20060270911 Applic. Date: 2006-10-02
Inventor: SUGAHARA KAZUYUKI [JP]
Application No.: US20070232596A1 Published: 04/Oct/2007Title: Benzothienopyridines for Use as Inhibitors of Eg5 Kinesin
Applicant/Assignee: ALTANA PHARMA AG 4SC AG
Application No.: 11/659738 Filing Date: 17/Aug/2005
Abstract:Compounds of the formula (1) in which R1, R2, R3, R4 and X have the meanings indicated in the description, are novel effective compounds with Eg5 inhibitory, anti-proliferative and/or apoptosis inducing activity.
Priority: EP20040103958 Applic. Date: 2004-08-18; EP20040104175 Applic. Date: 2004-08-31; WO2005EP54054 Applic. Date: 2005-08-17
Inventor: VENNEMANN MATTHIAS [DE]; BAER THOMAS [DE]; GROEGOR GUDRUN [DE]; BRAUNGER JURGEN [DE]; GIMMNICH PETRA [DE]; MAIER THOMAS [DE]; ROTHFELS HEIKE [DE]
Application No.: US20070232616A1 Published: 04/Oct/2007Title: Benzoimidazol-2-yl pyridines as modulators of the histamine H4 receptor
Applicant/Assignee: JANSSEN PHARMACEUTICA, N.V
Application No.: 11/731048 Filing Date: 30/Mar/2007
Abstract:Benzoimidazol-2-yl pyridines, pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by H4 receptor activity, including allergy, asthma, autoimmune diseases, and pruritis.
Priority: US20060788188P Applic. Date: 2006-03-31
Inventor: EDWARDS JAMES P [US]; KINDRACHUK DAVID E [US]; VENABLE JENNIFER D [US]
Application No.: US20070233036A1 Published: 04/Oct/2007Title: Eustachian Tube Device and Method
Applicant/Assignee:
Application No.: 11/678919 Filing Date: 26/Feb/2007
Abstract:Devices are provided for insertion into a Eustachian tube of an animal, e.g., a human being. The devices may include an insertable member, an immobilizing means and a fluid-communication providing means. The member has opposing surfaces and is formed at least in part from a biocompatible material that is degradable. The fluid-communication providing means is effective to provide sufficient fluid communication between the opposing surfaces of the insertable member to effect pressure equilibration therebetween. The immobilizing means is effective to immobilize the device within the Eustachian tube for a predetermined period. Also provided are kits that include the device and methods for inserting the device into a Eustachian tube.
Priority: US20060767020P Applic. Date: 2006-02-27
Inventor: MANDPE ADITI H [US]
Application No.: US20070237724A1 Published: 11/Oct/2007Title: Foamable suspension gel
Applicant/Assignee:
Application No.: 11/730011 Filing Date: 29/Mar/2007
Abstract:The present subject matter provides foamable suspension gels that foam after release from a container. The foamable suspension gels contain at least one pharmaceutically active agent that is sparingly soluble to insoluble in water, a second pharmaceutically active agent, and optionally a third active agent.
Priority: US20060744082P Applic. Date: 2006-03-31
Inventor: ABRAM ALBERT Z [AU]; FUCHSHUBER LILIAN [AU]
Application No.: US20070237731A1 Published: 11/Oct/2007Title: Nanoemulsion, production method thereof and cosmetic and dermatological composition containing it
Applicant/Assignee:
Application No.: 11/706763 Filing Date: 15/Feb/2007
Abstract:This invention comprehends a nanoemulsion based on an emulsifier ternary system that is stable under different temperature and physical stress conditions, besides being compatible with a great variety of cosmetics ingredients. The production method thereof comprises cold emulsification and homogenization steps, which make possible the incorporation of active oily ingredients sensitive to higher temperatures. The obtainment of the nanoemulsion with the properties of this invention comprehends the use of lecithin, of a fatty acid ester and sorbitol condensed with ethylene oxide and a ester of fatty acid and sugar, in specific proportions, as emulsifiers. Such nanoemulsion can be used in cosmetic and dermatological compositions aimed for care, protection and makeup of skin, mucosa, scalp and hair.
Priority: BR2006PI00941 Applic. Date: 2006-03-30
Inventor: DE OLIVEIRA PRAES CARLOS E [BR]; MOTTA FABRICIO C [BR]; FEFERMAN ISRAEL H S [BR]; DA SILVA BELLETTI KLEZIA M [BR]; KRUGER ODIVANIA [BR]; PATRIARCA PAOLA M [BR]; OLIVEIRA MENDES TANIA R [BR]; PIACESKI ANGELA D [BR]; SAUERMAN RONIT M [BR]
Application No.: US20070237734A1 Published: 11/Oct/2007Title: ANTI-WRINKLE COSMETIC COMPOSITION
Applicant/Assignee: L'OREAL
Application No.: 11/733797 Filing Date: 11/Apr/2007
Abstract:The present invention relates to adenosine derivatives and methods of treating skin using such derivatives.
Priority: FR20060051327 Applic. Date: 2006-04-11; US20060792328P Applic. Date: 2006-04-17
Inventor: DALKO MARIA [FR]; FAGOT DOMINIQUE [FR]
Application No.: US20070237735A1 Published: 11/Oct/2007Title: Anti-aging composition, kit and method of use
Applicant/Assignee: LABORATOIRES DERMO-COSMETIK INC
Application No.: 11/393811 Filing Date: 31/Mar/2006
Abstract:An anti-aging composition comprising: (i) at least one biomimetic oligopeptide having a sequence of 20 amino acids or less
(ii) at least one lipoaminoacid
(iii) at least one pentacyclic triterpenoid selected from the group consisting of asiaticoside, madecassic acid, asiatic acid and madecassoside
(iv) at least one antioxidant
and (v) tetrahydropiperine
a kit comprising such composition and a method of use.
Priority:
Inventor: DENOMMEE SYLVIE [CA]
Application No.: US20070237800A1 Published: 11/Oct/2007Title: MULTIPHASIC BIOFUNCTIONAL NANO-COMPONENTS AND METHODS FOR USE THEREOF
Applicant/Assignee:
Application No.: 11/763842 Filing Date: 15/Jun/2007
Abstract:Multiphasic nano-components (MPNs) having at least two phases and at least one active ingredient are provided. The MPNs can be used in various methods for medical diagnostics or with pharmaceutical, personal care, oral care, and/or nutritional compositions, for example, in oral care, hair, or skin products. The MPNs can be designed to have targeted delivery within an organism, while providing controlled release systems or combining incompatible active ingredients. Further, the MPNs can be used as biomedical coatings (such as anti-microbial coatings), or anti-corrosive coatings, bioimaging probes with combined diagnostic and therapeutic use, and fragrance release systems, among others. The MPNs can be formed by electrified jetting of polymers.
Priority: US2005-272194 Applic. Date: 2005-11-10; US20060814706P Applic. Date: 2006-06-16; US20040626792P Applic. Date: 2004-11-10; US20050651288P Applic. Date: 2005-02-09
Inventor: LAHANN JOERG [US]
Application No.: US20070237847A1 Published: 11/Oct/2007Title: Cosmetic Composition Comprising an Extract of the Leaves of the Castanea Sativa Plant and Cosmetic Treatments
Applicant/Assignee:
Application No.: 10/597964 Filing Date: 04/Feb/2005
Abstract:The present invention is concerned with a composition comprising an extract of the leaves of the plant Castanea sativa. It is furthermore concerned with the use of this extract for the manufacture of a cosmetic composition and with the use of this extract for the cosmetic treatment of the human body.
Priority: EP20040290388 Applic. Date: 2004-02-13; WO2005EP01105 Applic. Date: 2005-02-04
Inventor: HENRY FLORENCE [FR]; DANOUX LOUIS [FR]; PAULY GILLES [FR]
Application No.: US20070238718A1 Published: 11/Oct/2007Title: THIAZOLYL-DIHYDRO-INDAZOLE
Applicant/Assignee:
Application No.: 11/690351 Filing Date: 23/Mar/2007
Abstract:The present invention relates to new thiazolyl-dihydro-indazoles of general formula (I) wherein the groups R<1>, R<2 >and R<3 >have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-indazoles and the use thereof as pharmaceutical compositions.
Priority: EP20060112297 Applic. Date: 2006-04-06
Inventor: GRAUERT MATTHIAS [DE]; MAIER UDO [DE]; HOFFMANN MATTHIAS [DE]; SCHEUERER STEFAN [DE]; JOERGENSEN ANNE T [DE]; PAUTSCH ALEXANDER [DE]; BRANDL TRIXI [CH]; HOENKE CHRISTOPH [DE]; BREITFELDER STEFFEN [DE]; ERB KLAUS [DE]; PIEPER MICHAEL [DE]; PRAGST INGO [DE]
Application No.: US20070238730A1 Published: 11/Oct/2007Title: THIAZOLYL-DIHYDRO-CYCLOPENTAPYRAZOLE
Applicant/Assignee: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Application No.: 11/690356 Filing Date: 23/Mar/2007
Abstract:Disclosed are compounds of general formula (I), wherein the groups R<1>, R<2>, R have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-cyclopentapyrazoles and the use thereof as pharmaceutical compositions.Priority: EP20060112298 Applic. Date: 2006-04-06
Inventor: BREITFELDER STEFFEN [DE]; MAIER UDO [DE]; HOENKE CHRISTOPH [DE]; JOERGENSEN ANNE T [DE]; PAUTSCH ALEXANDER [DE]; BRANDL TRIXI [CH]; GRAUERT MATTHIAS [DE]; HOFFMANN MATTHIAS [DE]; SCHEUERER STEFAN [DE]; ERB KLAUS [DE]; PIEPER MICHAEL [DE]; PRAGST INGO [DE]
Application No.: US20070238746A1 Published: 11/Oct/2007
Title: THIAZOLYL-DIHYDRO-CHINAZOLINE
Applicant/Assignee:
Application No.: 11/690355 Filing Date: 23/Mar/2007
Abstract:Disclosed are compounds of general formula (I), wherein the groups A, R<1>, R<2> have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-quinazolines and the use thereof as pharmaceutical compositions.
Priority: EP20060112296 Applic. Date: 2006-04-06
Inventor: BRANDL TRIXI [CH]; MAIER UDO [DE]; HOENKE CHRISTOPH [DE]; JOERGENSEN ANNE T [DE]; PAUTSCH ALEXANDER [DE]; BREITFELDER STEFFEN [DE]; GRAUERT MATTHIAS [DE]; HOFFMANN MATTHIAS [DE]; SCHEUERER STEFAN [DE]; ERB KLAUS [DE]; PIEPER MICHAEL [DE]; PRAGST INGO [DE]
Application No.: US20070238771A1 Published: 11/Oct/2007Title: Indoles and benzoimidazoles as histamine H4 receptor modulators
Applicant/Assignee: JANSSEN PHARMACEUTICA, N.V
Application No.: 11/731047 Filing Date: 30/Mar/2007
Abstract:Benzoimidazole and indole compounds are described, which are useful as H4 receptor modulators. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by H4 receptor activity, such as allergy, asthma, autoimmune diseases, and pruritis.
Priority: US20060790421P Applic. Date: 2006-04-07
Inventor: EDWARDS JAMES P [US]; SAVALL BRAD M [US]; SHAH CHANDRAVADAN R [US]
Application No.: US20070238772A1 Published: 11/Oct/2007Title: Use of Metronidazole for Preparing a Pharmaceutical Composition for Treating a Cutaneous Vascularisation Disorder
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT, S.N.C
Application No.: 10/590074 Filing Date: 17/Feb/2005
Abstract:The invention relates more particularly to the use of metronidazole for the preparation of a pharmaceutical composition for treating a cutaneous vascularization disorder.
Priority: FR20040001720 Applic. Date: 2004-02-20; WO2005FR00369 Applic. Date: 2005-02-17
Inventor: DOLFI FABRIZIO [FR]; SAFONOVA IRINA [FR]
Application No.: US20070243132A1 Published: 18/Oct/2007Title: Transdermal delivery of pharmaceutical agents
Applicant/Assignee: APOLLO LIFE SCIENCES LIMITED
Application No.: 11/645122 Filing Date: 22/Dec/2006
Abstract:The present invention generally relates to a vehicle useful for delivering a pharmaceutically active compound including a genetic molecule or composition. More particularly, the present invention provides microemulsions for transdermal delivery of pharmaceutically active agents to a subject.
Priority: AU20060905107 Applic. Date: 2006-09-15; US20050753454P Applic. Date: 2005-12-22
Inventor: RUSSELL-JONES GREGORY J [AU]; LUKE MICHAEL R [AU]; HIMES STEWART R [AU]
Application No.: US20070243147A1 Published: 18/Oct/2007Title: Skin and/or Hair Composition Containing Compounds for Increasing The Tanning of Skin
Applicant/Assignee: BEIERSDORF AG
Application No.: 11/632188 Filing Date: 01/Jun/2005
Abstract:The invention relates to agents that are to be applied to the skin or hair and contain compounds for intensifying tanning of the skin and increasing melanin synthesis in skin or hair. The invention particularly relates to cosmetic or dermatological preparations. Using said preparations results in inducing and intensifying the tanning mechanisms of the skin, intensifying the hair color, and thus also increasing intrinsic protection of the skin or hair.
Priority: DE200410036092 Applic. Date: 2004-07-24; WO2005EP52493 Applic. Date: 2005-06-01
Inventor: WOLBER RAINER [DE]; TOM DIECK KAREN [DE]; SCHERNER CATHRIN [DE]; SCHLENZ KATHRIN [DE]; KRUSE INGE [DE]
Application No.: US20070243148A1 Published: 18/Oct/2007Title: PROTECTING AND REGENERATING COMPOSITION
Applicant/Assignee: LVMH RECHERCHE
Application No.: 11/668912 Filing Date: 30/Jan/2007
Abstract:The invention relates to a protecting and regenerating composition. This composition comprises an association of a first cosmetically active ingredient comprising a dried vine shoot extract, and a second cosmetically active ingredient comprising a component of the ectoine type. This composition makes it possible to affect anti-ageing cosmetic care and skin revitalization.
Priority: FR20060050400 Applic. Date: 2006-02-03
Inventor: ANDRE PATRICE [FR]; RENIMEL ISABELLE [FR]
Application No.: US20070243181A1 Published: 18/Oct/2007Title: Irak1c Splice Variant And Its Use
Applicant/Assignee: JANSSEN PHARMACEUTICA N.V
Application No.: 11/659168 Filing Date: 02/Aug/2005
Abstract:IRAK 1c splice variants and their preparation and use are described. The splice variants may be used in drug screening assays and methods for diagnosing medical conditions mediated by IRAK1c-modulating activity.
Priority: US20040598407P Applic. Date: 2004-08-02; WO2005US27656 Applic. Date: 2005-08-02
Inventor: LEUNG WAI-PING [US]; RAO NAVIN [US]
Application No.: US20070243216A1 Published: 18/Oct/2007Title: Stable solutions of prostaglandin and uses of same
Applicant/Assignee:
Application No.: 11/404657 Filing Date: 14/Apr/2006
Abstract:Dosage forms of a pharmaceutical composition comprising a sealed actives compartment containing a stable prostaglandin in a pharmaceutical composition for topical application to a patient are disclosed. Preferably, the prostaglandin compound is substantially uniformly dispersed in a delivery vehicle, and in certain embodiments the prostaglandin compound contains stabilizing agent comprising a moisture scavenger, an antioxidant and a chelating agent for metal ions. In certain embodiments the delivery vehicle is preferably substantially anhydrous, free of metal ions and oxygen and water. The improved compositions of the present invention are useful for treating medical conditions by providing a packed mono or multi-component dosage form that comprises a sealed section containing an active pharmaceutical ingredient and a delivery vehicle pharmaceutically compatible for topical delivery. The medical condition can be, for example male or female sexual dysfunction broadly and male erectile dysfunction specifically. Alternately, the medical condition can be a wound or other conditions such as hemorrhoids. In preferred embodiments of the medical treatment methods the active pharmaceutical ingredient is prostaglandin, and most preferably, the prostaglandin is treated with a stabilizing agent comprising a moisture scavenger, an antioxidant and a chelating agent for metal ions. In a specific application of the foregoing, a sock saturated with a gel forming material acting as lubricant is also disclosed which preferably has at least one wound healing composition to treat a foot skin condition, preferably using a wound healing composition such as prostaglandin.
Priority:
Inventor: KEPKA STANLEY [US]; BOCHENEK WIESLAW [US]
Application No.: US20070243221A1 Published: 18/Oct/2007Title: ANTI-WRINKLE COMPOSITION
Applicant/Assignee: L'OREAL
Application No.: 11/733786 Filing Date: 11/Apr/2007
Abstract:The present invention relates to the cosmetic use of at least one 4-aminopiperidine compound of formula (I) in which: Alk1 and Alk2 denote a C1-C10 alkylene radical
Ar1 denotes a phenyl group optionally substituted with one or more radicals, which may be identical or different, chosen from -F, -CF3, -R1, -OR1, -NR1R2
Ar2 denotes a phenyl group optionally substituted with one or more radicals, which may be identical or different, chosen from -F, -CF3, -NR1R2
R denotes a hydrogen atom or a C1-C10 alkyl radical
R1 and R2 denoting a C1-C7 alkyl radical
and the salts, optical isomers and solvates thereof, as an agent for combating wrinkles, especially expression wrinkles, and/or for decontracting the skin and/or relaxing the features. The invention also relates to a cosmetic composition containing such a compound and to the corresponding novel compounds.
Priority: FR20060051315 Applic. Date: 2006-04-11; US20060792327P Applic. Date: 2006-04-17
Inventor: CAVEZZA ALEXANDRE [FR]; BRETON PHILIPPE [FR]; DALKO MARIA [FR]
Application No.: US20070243240A1 Published: 18/May/2006Title: Transdermal therapeutic system
Applicant/Assignee:
Application No.: 11/087754 Filing Date: 24/Mar/2005
Abstract:The invention concerns a transdermal therapeutic system containing ergoline derivatives, preferably lisuride, with a stabilized ergoline compound. Stabilization of the oxidation sensitive ergoline combination is done through a combination of at least one fat-soluble, radical-trapping antioxidant, preferably Di-tert.-butylmethylphenols, Di-tert.-butylmetoxyphenols, tocopherols or ubichinones and a basic polymer. Use of a transdermal therapeutic system (TTS) comprising a pharmaceutical layer containing at least one matrix having an active ingredient and/or an active ingredient reservoir
a diffusion barrier that is permeable to said active ingredient and arranged on the skin side of the active ingredient reservoir
and an ergoline derivative or salt thereof as an active ingredient for producing an agent for obtaining and maintaining the circadian rhythm under dopamine therapy.
The invention relates to the use of a transdermal therapeutic system (TTS) comprising a medicinal layer, which contains at least one matrix comprising an active ingredient and/or an active ingredient reservoir and a diffusion barrier situated on the skin side of the active ingredient reservoir and permeable to active ingredients, in addition to, an ergoline-derivative or physiologically compatible salt with an acid thereof, as an active ingredient, for producing a means for treating the Restless Leg Syndrome and Periodic Limb Movement Disorder.
The invention relates to the use of a dopamine agonist in the form of an agent consisting of at least two spatially discrete compositions, of which one is a transdermal therapeutic system (TTS) containing the dopaminergic agent and another one or more are preparations for oral and/or parenteral application containing that same dopaminergic agent for the treatment of dopaminergically treatable diseases with the following elements: a) the TTS is continuously applied, b) within the duration of application in a) the composition for oral or parenteral dosage is administered.
Priority: DE20001043321 Applic. Date: 2000-08-24; DE20031041317 Applic. Date: 2003-09-03; DE20001053397 Applic. Date: 2000-10-20; WO2004DE01133 Applic. Date: 2004-05-30; US2003-362248 Applic. Date: 2003-07-07; WO2001EP09824 Applic. Date: 2001-08-24; US2003-362183 Applic. Date: 2003-07-21; WO2001EP09823 Applic. Date: 2001-08-24; US2003-362182 Applic. Date: 2003-07-03; WO2001EP09826 Applic. Date: 2001-08-24
Inventor: WINDT-HANKE FRED [DE]; GUNTHER CLEMENS [DE]; HOROWSKI REINHARD [DE]; TACK JOHANNES [DE]; ENGFER ADALBERT [DE]; BOSTEDT KATALIN T [DE]; SCHENK DIRK [DE]
Application No.: US20070243241A1 Published: 18/Oct/2007Title: Silicone Vesicles Containing Actives
Applicant/Assignee:
Application No.: 11/578541 Filing Date: 19/Apr/2005
Abstract:A process for preparing a vesicle composition based upon mixing an organopolysiloxane having at least one hydrophilic substituent group, a water miscible volatile solvent, and water is disclosed. The vesicle compositions produced by the method are useful in various personal, household, and health care applications.
Priority: US20040563663P Applic. Date: 2004-04-20; US20040575915P Applic. Date: 2004-06-01; US20040611258P Applic. Date: 2004-09-17; US20040611229P Applic. Date: 2004-09-17; US20050659271P Applic. Date: 2005-03-07; WO2005US13326 Applic. Date: 2005-04-19
Inventor: LIN SHAOW [US]; POSTIAUX STEPHANIE [BE]
Application No.: US20070243266A1 Published: 18/Oct/2007Title: Fluorinated 4-Azasteroids as Androgen Receptor Modulators
Applicant/Assignee: MERCK & CO., INC
Application No.: 11/578755 Filing Date: 22/Apr/2005
Abstract:Compounds of structural formula I are modulators of the androgen receptor (AR) in a tissue selective manner. These compounds are useful in the enhancement of weakened muscle tone and the treatment of conditions caused by androgen deficiency or which can be ameliorated by androgen administration, including osteoporosis, osteopenia, glucocorticoid-induced osteoporosis, periodontal disease, bone fracture, bone damage following bone reconstructive surgery, sarcopenia, frailty, aging skin, male hypogonadism, postmenopausal symptoms in women, atherosclerosis, hypercholesterolemia, hyperlipidemia, obesity, aplastic anemia and other hematopoietic disorders, inflammatory arthritis and joint repair, HIV-wasting, prostate cancer, benign prostatic hyperplasia (BPH), cancer cachexia, Alzheimer's disease, muscular dystrophies, cognitive decline, sexual dysfunction, sleep apnea, depression,
premature ovarian failure, and autoimmune disease, alone or in combination with other active agents.
Priority: US20040566044P Applic. Date: 2004-04-28; WO2005US13775 Applic. Date: 2005-04-22
Inventor: MEISSNER ROBERT S [US]; PERKINS JAMES J [US]
Application No.: US20070243271A1 Published: 18/Oct/2007Title: Use of polyphenols to treat skin conditions
Applicant/Assignee:
Application No.: 11/810112 Filing Date: 04/Jun/2007
Abstract:A composition is provided to treat and/or prevent for treating skin conditions including fine lines and wrinkles, acne rosacea, surface irregularities of the skin and hyper-pigmentation melasma of the skin, which includes use of a topically applied composition such as an ointment, lotion, cream, serum, gel or pad applied formulation, containing an effective amount of polyphenols, such as green tea based polyphenols, including but not limited to catechins, such as epigallocatechin gallate (EGCG), epigallocatechin (EGC), epicathechin 3-gallate (ECG) and epicatechin (EC). The formulation is preferably composed of 90 percent polyphenol isolates, derived from green tea with potent antioxidant properties, to assist in minimizing free-radical induced skin damage.
Priority: US2003-341101 Applic. Date: 2003-01-13
Inventor: HERNANDEZ STEVEN [US]; SHAFFER BURT [US]
Application No.: US20070244059A1 Published: 18/Oct/2007Title: Method For Attentuating Virulence Of Microbial Pathogens And For Inhibiting Microbial Biofilm Formation
Applicant/Assignee:
Application No.: 10/565591 Filing Date: 22/Jul/2004
Abstract:The present invention relates to the use of the cyclic dinucleotide c-di-GMP and cyclic dinucleotide analogues thereof in a method for attenuating virulence of a microbial pathogen or for inhibiting or reducing colonization by a microbial pathogen. This method further inhibits microbial biofilm formation and is capable of treating bacterial infections. The microbial colonization or biofilm formation inhibited or reduced may be on the skin or on nasal or mucosal surface. The microbial colonization or biofilm formation inhibited can also be on the surfaces of medical devices, especially those in close contact with the patient, as well on the surfaces of industrial and construction material where microbial colonization and biofilm formation is of concern.
Priority: US20030490029P Applic. Date: 2003-07-28; WO2004US23498 Applic. Date: 2004-07-22
Inventor: KARAOLIS DAVID K [US]
Application No.: US20070244096A1 Published: 18/Oct/2007Title: Fused Bicyclic Nitrogen-Containing Heterocycles
Applicant/Assignee: JAPAN TOBACCO INC
Application No.: 11/743376 Filing Date: 02/May/2007
Abstract:Compounds, pharmaceutical compositions and methods that are useful in the treatment or prevention of metabolic and cell proliferative diseases or conditions are provided herein. In particular, the invention provides compounds which modulate the activity of proteins involved in lipid metabolism and cell proliferation.
Priority: US2003-720844 Applic. Date: 2003-11-21; US20020428600P Applic. Date: 2002-11-22
Inventor: FOX BRIAN M [US]; FURUKAWA NOBORU [JP]; HAO XIAOLIN [US]; IIO KIYOSEI [JP]; INABA TAKASHI [JP]; JACKSON SIMON M [US]; KAYSER FRANK [US]; LABELLE MARC [US]; LI KEXUE [US]; MATSUI TAKUYA [JP]; MCMINN DUSTIN L [US]; OGAWA NOBUYA [JP]; RUBENSTEIN STEVEN M [US]; SAGAWA SHOICHI [JP]; SUGIMOTO KAZUYUKI [JP]; SUZUKI MASAHIRO [JP]; TANAKA MASAHIRO [JP]; YE GUOSEN [US]; YOSHIDA ATSUHITO [JP]; ZHANG JIAN [US]
Application No.: US20070244104A1 Published: 18/Oct/2007Title: THIAZOLYL-DIHYDRO-QUINAZOLINE
Applicant/Assignee: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Application No.: 11/690362 Filing Date: 23/Mar/2007
Abstract:Disclosed are thiazolyl-dihydro-quinazolines of general formula (I) wherein the groups R<1 >to R<4 >have the meanings given in the claims and specification, the isomers thereof, and processes for preparing these compounds and their use as pharmaceutical compositions.
Priority: EP20060112300 Applic. Date: 2006-04-06
Inventor: BRANDL TRIXI [CH]; MAIER UDO [DE]; HOFFMANN MATTHIAS [DE]; SCHEUERER STEFAN [DE]; JOERGENSEN ANNE T [DE]; PAUTSCH ALEXANDER [DE]; BREITFELDER STEFFEN [DE]; GRAUERT MATTHIAS [DE]; HOENKE CHRISTOPH [DE]; ERB KLAUS [DE]; PIEPER MICHAEL [DE]; PRAGST INGO [DE]
Application No.: US20070244126A1 Published: 18/Oct/2007Title: Benzoimidazol-2-yl pyrimidines and pyrazines as modulators of the histamine H4 receptor
Applicant/Assignee: JANSSEN PHARMACEUTICA, N.V
Application No.: 11/731074 Filing Date: 30/Mar/2007
Abstract:Benzoimidazol-2-yl pyrimidines and pyrazines, pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by H4 receptor activity, including allergy, asthma, autoimmune diseases, and pruritis.
Priority: US20060788190P Applic. Date: 2006-03-31
Inventor: EDWARDS JAMES P [US]; KINDRACHUK DAVID E [US]; MAPES CHRISTOPHER M [US]; PIPPEL DANIEL J [US]; VENABLE JENNIFER D [US]
Application No.: US20070244127A1 Published: 18/Oct/2007Title: Stable Dosage Form of Phenylalanine Derivatives
Applicant/Assignee: WILEX AG
Application No.: 11/631891 Filing Date: 20/Sep/2005
Abstract:The invention relates to improved and stable pharmaceutical formulations of phenylalanine derivatives and the use thereof as urokinase inhibitors, particularly for the treatment of malignant tumors and tumoral metastases.
Priority: DE200410045720 Applic. Date: 2004-09-21; WO2005EP10143 Applic. Date: 2005-09-20
Inventor: SCHMALIX WOLFGANG [DE]; BURGLE MARKUS [DE]; KOCH KLAUS [DE]
Application No.: US20070244130A1 Published: 18/Oct/2007Title: Compounds and Compositions as Ppar Modulators
Applicant/Assignee: IRM LLC
Application No.: 11/597260 Filing Date: 24/May/2005
Abstract:The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPAR.
Priority: US20040574137P Applic. Date: 2004-05-24; US20050649671P Applic. Date: 2005-02-02; WO2005US18166 Applic. Date: 2005-05-24
Inventor: EPPLE ROBERT [US]; XIE YONGPING [US]; WANG XING [US]; COW CHRISTOPHER [US]; RUSSO ROSS [US]
Application No.: US20070244180A1 Published: 18/Oct/2007Title: Substituted indole derivatives
Applicant/Assignee: SALMEDIX, INC CEPHALON, INC
Application No.: 10/956668 Filing Date: 01/Oct/2004
Abstract:Provided herein are indole derivatives, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
Priority: US20030508592P Applic. Date: 2003-10-02; US20040556599P Applic. Date: 2004-03-26
Inventor: CHAO QI [US]; ELLIOTT GARY T [US]; LEONI LORENZO [CH]
Application No.: US20070244203A1 Published: 18/Oct/2007Title: Controlled-Release Composition for Topical Application and a Method of Delivering an Active Agent to a Substrate
Applicant/Assignee:
Application No.: 10/576991 Filing Date: 27/Oct/2004
Abstract:A controlled-release composition for topical application to a substrate includes an oil-in-water emulsion and an active agent incorporated into the oil-in-water emulsion. The oil-in-water emulsion is substantially free of lipophilic solvent and is formed by mechanical inversion of a water-in-oil emulsion. The water-in-oil emulsion includes a silicone component, a surfactant, and water. A method of delivering the active agent to the substrate provides the oil-in-water emulsion and incorporates the active agent into the oil-in-water emulsion for delivery of the active agent to the substrate upon application of the oil-in-water emulsion to the substrate.
Priority: US20030514709P Applic. Date: 2003-10-27; WO2004US35619 Applic. Date: 2004-10-27
Inventor: RAUL VICTOR A [US]; THOMAS XAVIER J [FR]; SHIM ANNE K [US]; SCHALAU II GERALD K [US]; CABALA JANELLE L [US]
Application No.: US20070244204A1 Published: 18/Oct/2007Title: Rheology enhancers in non-oilfield applications
Applicant/Assignee:
Application No.: 11/403713 Filing Date: 13/Apr/2006
Abstract:A method for increasing the rate of shear rehealing of fluids made with cationic, zwitterionic, and amphoteric viscoelastic surfactant fluid systems by adding an effective amount of a rheology enhancer package containing, for example a polyethylene glycol-polypropylene glycol block copolymer and a polynaphthalene sulfonate. The rheology enhancer package allows viscoelastic surfactant fluids to be used at lower viscoelastic surfactant concentrations in certain non-oilfield excavation applications, for example boring, excavating, drilling and trenching operations in deep foundation construction, subterranean construction, and tunneling. Preferred surfactants are betaines and quaternary amines.
Priority:
Inventor: PRAT EVELYNE [FR]; DAHANAYAKE MANILAL S [US]; COLACO ALLWYN [US]; TILLOTSON ROBERT J [US]; LI FANG [US]
Application No.: US20070244294A1 Published: 18/Oct/2007Title: POLYAMIDE-POLYETHER BLOCK COPOLYMER
Applicant/Assignee:
Application No.: 11/753447 Filing Date: 24/May/2007
Abstract:Copolymers having linked internal polyether blocks and internal polyamide blocks have advantageous physical properties and solvent-gelling abilities. The copolymer may be prepared from a reaction mixture that contains 1,4-cyclohexane dicarboxylic acid (CHDA) and poly(alkyleneoxy) diamine (PAODA). Optionally, the reaction mixture contains no monofunctional compound reactive with either amine or carboxylic acid groups, however some of this monofunctional compound may be present. Dimer diamine and/or dimer acid may be present in the reaction mixture. A copolymer may also be prepared from a reaction mixture containing dimer acid and at least two diamine compound(s) including PAODA and short-chain aliphatic diamine having 2-6 carbons (SDA), wherein: a) the reaction mixture comprises x grams of PAODA and y grams of SDA, and x/(x+y) is 0.8-0.98
b) the reaction mixture weighs z grams, and x/z is at least 0.25
and c) the reaction mixture contains either no co-diacid, or comprises a small amount of co-diacid, wherein, if the reaction mixture comprises a small amount of co-diacid, then acid equivalents from co-diacid contribute less than 25% of the total acid equivalents present in the reaction mixture.
Priority: US2005-252441 Applic. Date: 2005-10-18; US2003-395050 Applic. Date: 2003-03-20
Inventor: PAVLIN MARK S [US]
Application No.: US20070247422A1 Published: 25/Oct/2007Title: Interaction techniques for flexible displays
Applicant/Assignee: XUUK, INC
Application No.: 11/731447 Filing Date: 30/Mar/2007
Abstract:The invention relates to a set of interaction techniques for obtaining input to a computer system based on methods and apparatus for detecting properties of the shape, location and orientation of flexible display surfaces, as determined through manual or gestural interactions of a user with said display surfaces. Such input may be used to alter graphical content and functionality displayed on said surfaces or some other display or computing system.
Priority: US20060788405P Applic. Date: 2006-03-30
Inventor: VERTEGAAL ROEL [CA]; HOLMAN DAVID [DE]
Application No.: US20070248551A1 Published: 25/Oct/2007Title: Use as an Antiperspirant Agent of a Flocculating Water-Soluble Polymer
Applicant/Assignee:
Application No.: 11/628761 Filing Date: 26/Apr/2005
Abstract:The present invention relates to the use of a flocculating water-soluble polymer comprising amine groups borne by a side substituent directly attached to the main chain, as an antiperspirant active agent in a cosmetic composition and particularly in a cosmetic composition not containing any antiperspirant aluminum and/or zirconium salts. The present invention also relates to a cosmetic process for treating perspiration, which consists in applying to the surface of the skin an effective amount of a flocculating water-soluble polymer comprising amine groups borne by a side substituent directly attached to the main chain.
Priority: FR20040051140 Applic. Date: 2004-06-09; US20040587041P Applic. Date: 2004-07-13; WO2005EP05243 Applic. Date: 2005-04-26
Inventor: LEMOINE CYRIL [FR]; BEAU NATHALIE [FR]
Application No.: US20070248556A1 Published: 25/Oct/2007Title: Administration of C-glycoside compounds for activating and regulating cutaneous immunity
Applicant/Assignee: L'OREAL
Application No.: 11/783411 Filing Date: 09/Apr/2007
Abstract:C-glycoside compounds having the general formula (1): are useful for stimulating the immune system of the skin and/or as immunoregulators, and are advantageously formulated into cosmetic/pharmaceutical compositions suited for preventing and/or limiting cutaneous immune imbalances, notably those resulting from environmental stresses.
Priority: FR20060051265 Applic. Date: 2006-04-07; US20060797390P Applic. Date: 2006-05-04
Inventor: PINEAU NATHALIE [FR]; DALKO MARIA [FR]
Application No.: US20070248633A1 Published: 25/Oct/2007Title: COMPOSITIONS CONTAINING A HYDROXYLATED DIPHENYLMETHANE COMPOUND, METHODS OF USE
Applicant/Assignee: L'OREAL
Application No.: 11/738568 Filing Date: 23/Apr/2007
Abstract:The invention relates to a composition containing, in a physiologically acceptable medium, (a) at least one hydroxylated diphenylmethane compound of formula (I) where formula variables are defined in the body of the application and claims and (b) at least one ingredient promoting the solubilization, stabilization and/or activity of the hydroxylated diphenylmethane compound of formula (I). The invention also relates to a cosmetic method for caring for or making up the skin, comprising the topical application of such a composition to the skin.
Priority: FR20060051417 Applic. Date: 2006-04-21; US20060796589P Applic. Date: 2006-05-02
Inventor: BALDO FRANCINE [FR]
Application No.: US20070248635A1 Published: 25/Oct/2007Title: GREEN TEA JEWELRY
Applicant/Assignee: SOUTHERLEE INCORPORATED
Application No.: 11/379556 Filing Date: 20/Apr/2006
Abstract:A method for making green tea jewelry is provided. The jewelry may be worn as a transdermal source of green tea components used as an alternative to or in addition to ingestion of green tea liquid or solids. Also provided is a kit for providing green tea jewelry in a substantially water resistant and air-tight package. The kit may comprise additional articles such as informational inserts and scents.
Priority:
Inventor: JENSEN DAVID M [US]
Application No.: US20070248658A1 Published: 25/Oct/2007Title: Use of film-forming hair care polymers from the group of polyurethanes and pharmaceutical preparations and patches that contain these polymers
Applicant/Assignee:
Application No.: 11/643948 Filing Date: 22/Dec/2006
Abstract:The subject of this application is the use of film-forming polyurethanes that are used in hair care agents or mixtures of these polyurethanes with other polymers in pharmaceutical preparations for dermal or transdermal administration of active ingredients, as well as patches and pharmaceutical preparations that contain these hair care polyurethanes.
Priority: EP20060090023 Applic. Date: 2006-02-03; EP20050090347 Applic. Date: 2005-12-23; US20060764796P Applic. Date: 2006-02-03
Inventor: ZURDO SCHROEDER INES [DE]; FRANKE PATRICK [DE]; BRACHT STEFAN [DE]
Application No.: US20070248705A1 Published: 25/Oct/2007Title: Agents for Activating the Transcription Factor Nrf2 and Foods Having Such Function
Applicant/Assignee: KIRIN BEER KABUSHIKI KAISHA
Application No.: 11/577583 Filing Date: 21/Oct/2005
Abstract:A composition, an Nrf2 activating agent, and a food according to the present invention comprise isohumulones or isomerized hop extract as an active ingredient. They are useful in treating, preventing, or ameliorating a disease of condition which is treatable, preventable, or ameliorable by the activation of transcription factor Nrf2. More specifically, the composition, the Nrf2 activating agent and the food according to the present invention are useful in treating, preventing, ameliorating, or alleviating chronic diseases which are believed to be caused or exacerbated by cellular damages due to oxidative stress in the body or environmental substances (for example, arteriosclerosis, hypertension, diabetes, cerebral nerve degenerative diseases, skin diseases, eye diseases, asthma, and cancer) or delaying progress of these diseases, or in detoxificating xenobiotic substances.
Priority: JP20040307838 Applic. Date: 2004-10-22; WO2005JP19415 Applic. Date: 2005-10-21
Inventor: SHIMURA MASAKO [JP]; YOSHIDA ARUTO [JP]
Application No.: US20070249571A1 Published: 25/Oct/2007Title: Novel conjugate compounds and dermatological compositions thereof
Applicant/Assignee: TAMARKIN PHARMACEUTICALS
Application No.: 11/819258 Filing Date: 26/Jun/2007
Abstract:The invention relates to novel cosmetic and dermatological compositions, comprising conjugate compounds, including a dicarboxylic acid moiety, which is covalently linked through covalent bonds to a biologically active alcohol, selected from the group of steroidal hormones, steroidal anti-inflammatory agents, vitamin E and vitamin D.
Priority: US2003-737181 Applic. Date: 2003-12-16; US20020433829P Applic. Date: 2002-12-16
Inventor: TAMARKIN DOV [IL]
Application No.: US20070249611A1 Published: 25/Oct/2007Title: DIPEPTIDYL PEPTIDASE INHIBITORS
Applicant/Assignee:
Application No.: 11/691709 Filing Date: 27/Mar/2007
Abstract:Compounds, pharmaceutical compositions, kits and methods are provided for use with DPP-IV and other S9 proteases that comprise a compound of the formula: wherein the substituents are as defined herein.
Priority: US20060787047P Applic. Date: 2006-03-28
Inventor: FENG JUN [US]; GWALTNEY STEPHEN L [US]; WALLACE MICHAEL B [US]; ZHANG ZHIYUAN [US]
Application No.: US20070249714A1 Published: 25/Oct/2007Title: Method of treating skin requiring fractional resurfacing treatment
Applicant/Assignee:
Application No.: 11/647663 Filing Date: 29/Dec/2006
Abstract:A treatment regimen for treating skin subject to fractional resurfacing procedures involves the application of supplemental composition(s) such as preparatory composition(s), protective composition(s), and combinations thereof, and a corrective composition.
Priority: US20050755464P Applic. Date: 2005-12-30
Inventor: HATTENDORF JUDY [US]; CARLSON STEVE [US]
Application No.: US20070249795A1 Published: 25/Oct/2007Title: Photopolymerisable materials for use in wound dressing
Applicant/Assignee:
Application No.: 11/573833 Filing Date: 03/Jun/2005
Abstract:A composition that is photopolymerisable in the presence of water comprising: (a) a first water-soluble monomer having olefinic unsaturation and a flexible hydrophilic chain
(b) from 0.2 to 20 parts by weight, based on the weight of the first monomer, of a second water soluble monomer having olefinic unsaturation and a group that imparts tackiness on curing, and which is of high free radical polymerization efficiency
(c) from 0.001 to 0.5 parts by weight, based on the weight of the first monomer, of a cross-linking agent
(d) from 0.001 to 0.5 parts by weight, based on the weight of the first monomer, of a photoinitiator
and (e) from greater than 20% up to 50% by weight, based on the total weight of the composition, of a low molecular weight polyol.
Priority: GB20040018522 Applic. Date: 2004-08-19; WO2005GB02196 Applic. Date: 2005-06-03
Inventor: TAKTAK YOUSEF S [GB]
Application No.: US20070249805A1 Published: 25/Oct/2007Title: CLAY-BINDING PEPTIDES AND METHODS OF USE
Applicant/Assignee: E.I. DU PONT DE NEMOURS AND COMPANY
Application No.: 11/696380 Filing Date: 04/Apr/2007
Abstract:Combinatorially generated peptides are provided that have binding affinity for clay. The peptides may be used to deliver benefit agents to various clay surfaces.
Priority: US20060790149P Applic. Date: 2006-04-06
Inventor: ITTEL STEVEN D [US]; CUNNINGHAM SCOTT D [US]; ROUVIERE PIERRE E [US]; FAHNESTOCK STEPHEN R [US]; O'BRIEN JOHN P [US]; SCHNEIDER EBERHARD [DE]; SCHURMANN GREGOR [DE]; WAGNER PETER [DE]
Application No.: US20070251020A1 Published: 01/Nov/2007Title: Fungicidal compositions and methods of using the same
Applicant/Assignee:
Application No.: 11/789543 Filing Date: 25/Apr/2007
Abstract:Methods of preventing or inhibiting putrefaction, degradation, and/or deterioration of a surface of wet animal hide or skin are described. The method can include applying a composition containing at least one minimum risk fungicide to the surface or to a solid, liquid or gas that comes in contact with the surface. Treated hides or skin are further described.
Priority: US20060795864P Applic. Date: 2006-04-28
Inventor: STOCKMAN GEORGE B [US]; OPPONG DAVID [US]
Application No.: US20070253911A1 Published: 01/Nov/2007Title: Foamable compositions, kits and methods for hyperhidrosis
Applicant/Assignee: FOAMIX LTD
Application No.: 11/717897 Filing Date: 13/Mar/2007
Abstract:The composition of the present invention is geared towards treating hyperhidrosis or any condition involving and/or promoting excessive sweating, typically involving the whole body, include hyperthyroidism or similar endocrine disorders
endocrine treatment for prostatic cancer or other types of malignant disorder
severe psychiatric disorders
obesity and menopause. The foamable composition of the present invention is suitable for treating palmar hyperhidrosis
axillary hyperhidrosis
plantar hyperhidrosis
hyperhidrosis of the trunk and/or the thighs
and facial hyperhidrosis
and any combination of them consisting of a therapeutic foamable composition including: an active agent, suitable for the treatment or prevention of hyperhidrosis.
Priority: IL20020152486 Applic. Date: 2002-10-25; US2004-911367 Applic. Date: 2004-08-04; US2005-532618 Applic. Date: 2005-12-22; WO2003IB05527 Applic. Date: 2003-10-24; US2005-078902 Applic. Date: 2005-03-11; US20030492385P Applic. Date: 2003-08-04; US20020429546P Applic. Date: 2002-11-29; US20060781868P Applic. Date: 2006-03-13; US20070897638P Applic. Date: 2007-01-26; US20070899176P Applic. Date: 2007-02-02
Inventor: TAMARKIN DOV [IL]; EINI MEIR [IL]; ZLATKIS ELLA [IL]
Application No.: US20070253923A1 Published: 01/Nov/2007Title: Personal Care Composition
Applicant/Assignee:
Application No.: 11/632026 Filing Date: 22/Jul/2005
Abstract:A personal care composition comprising a cationically modified cellulose ether, wherein the cellulose ether comprises from 0.5 to 4 moles of an ether substituent per mole of anhydroglucose repeat unit and the cellulose ether is further substituted with a cationic substituent of the formula (I) wherein R<1>, R<2 >and R<3 >each independently are CH3 or C2H5, R<4 >is CH2-CHOH-CH2 or CH2CH2, A is an anion, and z is 1, 2 or 3, and the cellulose ether comprises from 1.15 to 1.44 percent of cationic nitrogen, based on the total weight of the cellulose ether. The cationically modified cellulose ethers which comprise from 6,000 to 15,000 anhydroglucose repeat units are novel.Priority: US20040601889P Applic. Date: 2004-08-16; WO2005US26115 Applic. Date: 2005-07-22
Inventor: ZHANG XIAODONG [US]; KREEGER RUSSELL L [US]; DROVETSKAYA TATIANA V [US]
Application No.: US20070254044A1 Published: 01/Nov/2007Title: Antimicrobial Amorphous Compositions
Applicant/Assignee: ACRYMED, INC
Application No.: 11/663236 Filing Date: 19/Sep/2005
Abstract:The present invention comprises compositions and methods for providing antimicrobial compositions. The antimicrobial compositions comprise gel delivery vehicles comprising stabilized silver, wherein ionic silver is provided to a site for antimicrobial purposes. Methods of making and using such compositions are taught, including application of the silver-containing gel compositions to wounds, burns, abrasions, cuts, surgical incision, sites where skin or organ integrity has been breached, and other sites to supply an antimicrobial environment.
Priority: US20040611486P Applic. Date: 2004-09-20; WO2005US33600 Applic. Date: 2005-09-19
Inventor: KARANDIKAR BHALCHANDRA M [US]; GIBBINS BRUCE L [US]
Application No.: US20070254046A1 Published: 01/Nov/2007Title: Novel Pyrazolopyrimidines
Applicant/Assignee: ALTANA PHARMA AG BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Application No.: 11/661111 Filing Date: 05/Sep/2005
Abstract:Compounds of a certain formula I in which R1, R2, R3 and R4 have the meanings indicated in the description are novel compounds expected to be useful in the therapy of (hyper)proliferative diseases and/or disorders responsive to induction of apoptosis.
Priority: EP20040104283 Applic. Date: 2004-09-06; WO2005EP54366 Applic. Date: 2005-09-05
Inventor: MAIER THOMAS [DE]; ZUELCH ARMIN [DE]; CIOSSEK THOMAS [DE]; BAER THOMAS [DE]; BECKERS THOMAS [DE]
Application No.: US20070254052A1 Published: 01/Nov/2007Title: Substances capable of potentiating laminin 5 productivity in epidermal cells and their use
Applicant/Assignee:
Application No.: 11/819890 Filing Date: 29/Jun/2007
Abstract:The invention provides cosmetics or dermatological compositions comprising plant extract or whey extract having an action to potentiate laminin 5 productivity in the epidermal cells. They have mainly the action and efficacy to prevent or improve aging in the skin.
Priority: JP20010250285 Applic. Date: 2001-08-21; JP20010250289 Applic. Date: 2001-08-21; JP20010250295 Applic. Date: 2001-08-21; JP20020046014 Applic. Date: 2002-02-22; US2004-487277 Applic. Date: 2004-02-20; WO2002JP08402 Applic. Date: 2002-08-21
Inventor: TAKADA KEIKO [JP]; AMANO SATOSHI [JP]; NISHIYAMA TOSHIO [JP]
Application No.: US20070254920A1 Published: 01/Nov/2007Title: Prodrug derivatives of acids using alcohols with homotopic hydroxy groups and methods for their preparation and use
Applicant/Assignee: AERIE PHARMACEUTICALS, INC
Application No.: 11/412207 Filing Date: 26/Apr/2006
Abstract:This invention relates to novel homotopic prodrugs and medicaments and methods for their preparation, testing and use. In one embodiment, the homotopic prodrug has the general formula wherein is a biologically-active moiety comprising a carboxylic acid functional group, and Rb is a homotopically-symmetrical alcohol bonded to the biologically-active moiety through the carboxylic acid functional group to form an ester linkage, as well as optical isomers, enantiomers, pharmaceutically acceptable salts, biohydrolyzable amides, esters, and imides thereof and combinations thereof.
Priority:
Inventor: DELONG MITCHELL A [US]; MCFADDEN JILL M [US]; ROYALTY SUSAN M [US]; TOONE ERIC J [US]; YINGLING JEFFREY D [US]
Application No.: US20070254931A1 Published: 01/Nov/2007Title: Thiazole Derivatives Having Vap-1 Inhibitory Activity
Applicant/Assignee: ASTELLAS PHARMA INC
Application No.: 11/572772 Filing Date: 27/Jul/2005
Abstract:A compound of the formula (I), (II), (III) or (IV): wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof useful as a vascular adhesion protein-1 (VAP-1) inhibitor, a pharmaceutical composition, a method for preventing or treating a VAP-1 associated disease, especially macular edema, which method includes administering an effective amount of the compound or a pharmaceutically acceptable salt thereof to a subject, and the like.
Priority: AU20040904196 Applic. Date: 2004-07-27; WO2005JP14136 Applic. Date: 2005-07-27
Inventor: INOUE TAKAYUKI [JP]; TOJO TAKASHI [JP]; MORITA MASATAKA [JP]
Application No.: US20070255197A1 Published: 01/Nov/2007Title: Method of Treatment for Undesired Effect Following Transdermal or Topical Drug Delivery
Applicant/Assignee: ACRUX DDS PTY LTD
Application No.: 10/581991 Filing Date: 09/Dec/2004
Abstract:This invention relates to a method for inhibiting the percutaneous absorption of a physiologically active agent topically applied to a transdermal administration site of a subject, the method including the step of applying to skin of the subject at the transdermal administration site, a device ( 1, 7 ) comprising a membrane ( 8 ) for contacting the skin of the subject coated on the skin contacting side thereof ( 11 ) with a layer of an adhesive ( 10 ).
Priority: AU20030906842 Applic. Date: 2003-12-10; WO2004AU01738 Applic. Date: 2004-12-09
Inventor: HUMBERSTONE ANDREW J [AU]; WILKINS NINA F [AU]; GONDA IGOR [AU]
Application No.: US20070258911A1 Published: 08/Nov/2007Title: Method of producing high alcohol content foaming compositions with silicone-based surfactants
Applicant/Assignee:
Application No.: 11/806767 Filing Date: 04/Jun/2007
Abstract:This invention relates to a method of producing and dispensing a foam using a "high lower alcohol content"(>40% v/v of a C1-4 alcohol) liquid composition. The liquid compositions comprise an alcohol, C1-4(>40% v/v), a silicone-based surfactant of at least 0.001% by weight to prepare a foamable composition, 0-10% w/w of additional minor components added to obtain the desired performance (a foamable composition), and the balance being purified water. The compositions may include emulsifier-emollients and mosturizers, secondary surfactants, foam stabilizers, fragrances, antimicrobial agents, other type of medicinal ingredients, and the like ingredients or additives or combinations thereof commonly added to alcohol gels or foams, aerosol compositions or to toiletries, cosmetics, pharmaceuticals and the like.
Priority: US2006-591243 Applic. Date: 2006-03-07; WO2006CA00320 Applic. Date: 2006-03-07; US20050658580P Applic. Date: 2005-03-07
Inventor: FERNANDEZ DE CASTRO MARIA T [US]; KOLVISTO BRUCE M [US]; MUNOZ FRANCISCO [US]
Application No.: US20070258935A1 Published: 08/Nov/2007Title: Water dispersible films for delivery of active agents to the epidermis
Applicant/Assignee:
Application No.: 11/800722 Filing Date: 07/May/2007
Abstract:A water-dissipatable film forming formulation includes a polymer having at least one water solubilizing or dissipating moiety
an active ingredient or agent
and at least one of a plasticizer or a humectant. The present invention also includes a method for delivering an active agent to the epidermis of a subject. The method includes applying the film forming formulation to a predetermined area of skin.
Priority: US20060798574P Applic. Date: 2006-05-08
Inventor: MCENTIRE EDWARD ENNS [US]; STOCKL REBECCA REID [US]; MUNJAL RAMESH CHAND [US]; POSEY-DOWTY JESSICA DEE [US]; WATTERSON THELMA LEE [US]
Application No.: US20070259013A1 Published: 08/Nov/2007Title: Pharmaceutical compositions comprising silica microspheres
Applicant/Assignee:
Application No.: 11/783895 Filing Date: 12/Apr/2007
Abstract:The present invention relates to a topical composition which includes a bioactive drug formulated with silica in the form of microspheres, or drugs in a combination with the silica microspheres in an oily suspension, gel or emulsion. The topical compositions of the invention provide sustained release of a bioactive drug so as to reduce skin irritation.
Priority: US20060791902P Applic. Date: 2006-04-14; US20060817247P Applic. Date: 2006-06-29
Inventor: SHEVACHMAN MARINA [IL]; ZE EVI AMIRA [IL]; ASCULAI EILON [IL]; BINYAMINOVICH BATELLA [IL]
Application No.: US20070259029A1 Published: 08/Nov/2007Title: Water-dispersible patch containing an active agent for dermal delivery
Applicant/Assignee:
Application No.: 11/800727 Filing Date: 07/May/2007
Abstract:A dermal patch having comprising at least two layers wherein at least one layer is a polymer matrix system having an active agent admixed therein. At least one of the layers includes a water-dispersible or water-dissipatable polymer. The dermal patch has an elongation factor of at least 50%.
Priority: US20060798575P Applic. Date: 2006-05-08
Inventor: MCENTIRE EDWARD ENNS [US]; STOCKL REBECCA REID [US]; MUNJAL RAMESH CHAND [US]
Application No.: US20070259057A1 Published: 08/Nov/2007Title: Wrinkle Reduction Agent, Lipolysis Accelerator, Composition for External Use on Skin, and Food or Beverage Composition
Applicant/Assignee: KAO CORPORATION
Application No.: 11/661401 Filing Date: 29/Aug/2005
Abstract:An antiwrinkle agent, lipolysis promoter, external composition for skin, and food and beverage composition having for an active ingredient thereof a compound represented by general formula (1): (wherein R represents a hydrogen atom or an acyl group having 2 to 20 carbon atoms) or an extract obtained from guinea ginger and/or an acylation treatment product of said extract.
Priority: JP20040250178 Applic. Date: 2004-08-30; JP20040321698 Applic. Date: 2004-11-05; JP20050004506 Applic. Date: 2005-01-11; JP20050144765 Applic. Date: 2005-05-17; JP20050176165 Applic. Date: 2005-06-16; WO2005JP15635 Applic. Date: 2005-08-29
Inventor: SUGITA JUN [JP]; IKEMOTO TAKESHI [JP]; AKAZAWA YUMIKO [JP]; KOBAYASHI YURIE [JP]; MITANI MITSUMASA [JP]; HARATAKE AKINORI [US]; KOMIYA AYA [JP]
Application No.: US20070259354A1 Published: 08/Nov/2007Title: OPTIMIZED TRPM8 NUCLEIC ACID SEQUENCES AND THEIR USE IN CELL BASED ASSAYS AND TEST KITS TO IDENTIFY TRPM8 MODULATORS
Applicant/Assignee: SENOMYX, INC
Application No.: 11/536394 Filing Date: 28/Sep/2006
Abstract:Modified human TRPM8 nucleic acid sequences which are efficiently expressed in human cells and cell-based assays and test kits containing same are provided. These assays identify TRPM8 modulators using cells that express a modified human TRPM8 nucleic acid sequence according to the invention, wherein said sequence has been modified relative to a wild-type human TRPM8 nucleic acid sequence in order to optimize ion channel expression in desired cells. Assays using these modified TRPM8 sequences have been shown to identify compounds that modulate the human TRPM8 ion channel better or comparably to known coolants such as menthol and icilin.
Priority: US20050724776P Applic. Date: 2005-10-11; US20050724777P Applic. Date: 2005-10-11
Inventor: SERVANT GUY [US]; BRUST PAUL [US]; MOYER BRYAN [US]; LU MIN [US]; ECHEVERRI FERNANDO [US]; DAHAN DAVID [US]; ZOLLER MARK [US]; WILLIAMS MARK [US]; KIMMICH RACHEL [US]; KAMDAR POONIT [US]; DITSCHUN TANYA [US]; PATRON ANDREW [US]
Application No.: US20070259383A1 Published: 08/Nov/2007Title: Novel Genes involved in Epidermal differentiation, and uses thereof
Applicant/Assignee: EISAL R&D MANAGEMENT CO., LTD
Application No.: 10/591099 Filing Date: 02/Mar/2005
Abstract:A high-throughput in situ hybridization system was applied to the mouse foot pad epidermis to identify novel genes involved in epidermal differentiation. As a result, epidermal expression patterns were detected for about 100 unique mRNAs. Of these, two novel secreted proteins, dermokine-alpha and -beta, which are expressed in the suprabasal layer of the differentiated epithelia, were successfully identified. Further, the gene encoding the above proteins was found to constitute a novel gene complex (SSC).
Priority: JP20040057559 Applic. Date: 2004-03-02; WO2005JP03458 Applic. Date: 2005-03-02
Inventor: MATSUI TAKESHI [JP]; KISUMI FUMIE [JP]; KINOSHITA YOKO [JP]
Application No.: US20070259855A1 Published: 08/Nov/2007Title: THIAZOLYL-DIHYDRO-INDAZOLE
Applicant/Assignee:
Application No.: 11/690360 Filing Date: 23/Mar/2007
Abstract:Disclosed are compounds of general formula (I), wherein the groups R<1>, R<2> have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-indazoles and the use thereof as pharmaceutical compositions.
Priority: EP20060112299 Applic. Date: 2006-04-06
Inventor: MAIER UDO [DE]; GRAUERT MATTHIAS [DE]; HOFFMANN MATTHIAS [DE]; HOENKE CHRISTOPH [DE]; JOERGENSEN ANNE T [DE]; PAUTSCH ALEXANDER [DE]; BRANDL TRIXI [CH]; BREITFELDER STEFFEN [DE]; SCHEUERER STEFAN [DE]; ERB KLAUS [DE]; PIEPER MICHAEL [DE]; PRAGST INGO [DE]
Application No.: US20070259890A1 Published: 08/Nov/2007Title: Compounds and Compositions as Ppar Modulators
Applicant/Assignee: IRM LLC
Application No.: 11/596598 Filing Date: 13/May/2005
Abstract:The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPARdelta.
Priority: US20040571004P Applic. Date: 2004-05-14; WO2005US16747 Applic. Date: 2005-05-13
Inventor: EPPLE ROBERT [US]; AZIMIOARA MIHAI [US]
Application No.: US20070259904A1 Published: 08/Nov/2007Title: Bi-aryl meta-pyrimidine inhibitors of kinases
Applicant/Assignee: TARGEGEN, INC
Application No.: 11/796717 Filing Date: 26/Apr/2007
Abstract:The invention provides biaryl meta-pyrimidine compounds having the general structure (A). The pyrimidine compounds of the invention are capable of inhibiting kinases, such as members of the Jak kinase family, and various other specific receptor and non-receptor kinases.
Priority: US2006-588638 Applic. Date: 2006-10-26; US20050732629P Applic. Date: 2005-11-01; US20060838003P Applic. Date: 2006-08-15
Inventor: NORONHA GLENN [US]; MAK CHI C [US]; CAO JIANGUO [US]; RENICK JOEL [US]; MCPHERSON ANDREW [US]; ZENG BINQI [US]; PATHAK VED P [US]; LOHSE DANIEL L [US]; HOOD JOHN D [US]; SOLL RICHARD M [US]
Application No.: US20070261775A1 Published: 15/Nov/2007Title: Polystyrene binding peptides and methods of use
Applicant/Assignee: E.I. DU PONT DE NEMOURS AND COMPANY
Application No.: 11/607673 Filing Date: 01/Dec/2006
Abstract:Combinatorially generated peptides are provided that have binding affinity for polystyrene (PS). The peptides may be used to deliver benefit agents to various PS surfaces.
Priority: US20050750850P Applic. Date: 2005-12-15
Inventor: CUNNINGHAM SCOTT D [US]; LOWE DAVID J [US]; O'BRIEN JOHN P [US]; WANG HONG [US]; WILKINS ANTOINETTE E [US]
Application No.: US20070264204A1 Published: 15/Nov/2007Title: PERSONAL CARE COMPOSITIONS CONTAINING FUNCTIONALIZED POLYMERS
Applicant/Assignee: AIR PRODUCTS AND CHEMICALS, INC
Application No.: 11/747261 Filing Date: 11/May/2007
Abstract:The disclosure provides a personal care composition and method for forming the composition wherein the SCC polymer has at least one functionality selected from the group consisting of silicone, hydroxyl and carboxy. Such functionalized SCC polymers can be employed in a wide range of personal care compositions including skin care, body wash, and shampoo and hair treatments, among other personal care products.
Priority: US20060799616P Applic. Date: 2006-05-11; US20070900847P Applic. Date: 2007-02-12
Inventor: NOOR MUSSARAT [US]; LEMMA SOLOMON [US]
Application No.: US20070264208A1 Published: 15/Nov/2007Title: Cosmetic and/or pharmaceutical composition comprising at least one copolymer comprising at least one ionizable group, and cosmetic treatment process
Applicant/Assignee:
Application No.: 11/640420 Filing Date: 18/Dec/2006
Abstract:Disclosed herein is a cosmetic and/or pharmaceutical composition comprising, in a physiologically acceptable medium, at least one (co)polymer comprising a polymer backbone and at least one junction group linked to the polymer backbone and capable of establishing H bonds with at least one partner junction group, each pairing of a junction group involving at least 3 H bonds, wherein the at least one (co)polymer comprises at least one ionizable group. Also disclosed herein is a cosmetic treatment process comprising applying the composition to keratin materials.
Priority: FR20050053909 Applic. Date: 2005-12-16; US20050754183P Applic. Date: 2005-12-28
Inventor: MOUGIN NATHALIE [FR]; CHODOROWSKI-KIMMES SANDRINE [FR]; SCHULTZE XAVIER [FR]
Application No.: US20070264210A1 Published: 15/Nov/2007Title: Method of enhancing penetration of water-soluble actives
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/803532 Filing Date: 15/May/2007
Abstract:A method of enhancing the delivery of water-soluble skin care actives into keratinous tissue, comprising the step of applying to the keratinous tissue a water-in-oil emulsion comprising an aqueous phase and a non-aqueous phase, wherein the aqueous phase comprises a water-soluble skin care active, and whereupon application of shear stress to the composition, the aqueous phase is visibly separated from the non-aqueous phase.
Priority: US20060800378P Applic. Date: 2006-05-15
Inventor: ROBINSON LARRY RICHARD [US]
Application No.: US20070264295A1 Published: 15/Nov/2007Title: TOPICAL INSECT REPELLENT COMPOSITION AND METHOD OF APPLICATION
Applicant/Assignee: 3M INNOVATIVE PROPERTIES COMPANY
Application No.: 11/382976 Filing Date: 12/May/2006
Abstract:Stable, single phase, low VOC, topical insect repellent compositions containing a film-forming polymer, insect repellent, water miscible organic solvent, and water.
Priority:
Inventor: KANTNER STEVEN S [US]
Application No.: US20070264349A1 Published: 15/Nov/2007Title: Nano-structured compositions and methods of making and using the same
Applicant/Assignee: NOVAVAX, INC
Application No.: 11/714274 Filing Date: 06/Mar/2007
Abstract:The present invention provides a new tri-phasic method for making nanoparticles of poorly soluble active pharmaceutical ingredients.
Priority: US20060779420P Applic. Date: 2006-03-07; US20060837294P Applic. Date: 2006-08-14
Inventor: LEE ROBERT [US]; SHENOY DINESH [US]; WRIGHT D C [US]
Application No.: US20070264354A1 Published: 15/Nov/2007Title: TREATMENT OF A WOUND WITH A VASODILATOR
Applicant/Assignee:
Application No.: 11/745178 Filing Date: 07/May/2007
Abstract:A wound treatment administers a vasodilator by: (a) active transdermal treatment such as: by direct perfusion of the wound with the vasodilator, by an intradermal injection of the vasodilator about the wound and its surrounding skin area, by iontophoresis about the wound and its surrounding skin area with the vasodilator, by microdialysis of the wound with the vasodilator using one or more probe situated about the wound and its surrounding skin area
and/or by (b) passive transdermal treatment such as: by transcutaneous electrical stimulation (TENS) about the wound and its surrounding skin area while administering the vasodilator, or by a combination of the foregoing. The vasodilator can be calcitonin gene-related peptide (CGRP) with or without vasoactive intestinal polypeptide (VIP), nitric oxide (NO), nerve growth factor (NGF), or a combinations of the forgoing. Blood flow proximal the wound can be monitored during the treatment to derive a chemical/dose relationship of the vasodilator being administered in the treatment.
Priority: US20060746849P Applic. Date: 2006-05-09; US20070887756P Applic. Date: 2007-02-01
Inventor: HERMAN RICHARD M [US]
Application No.: US20070264368A1 Published: 15/Nov/2007Title: Carbohydrase inhibitors derived from fagaceous plants and use thereof
Applicant/Assignee:
Application No.: 11/662636 Filing Date: 03/Jun/2005
Abstract:The present invention provides a plant-derived carbohydrase inhibitor, wherein the inhibitor is effective for preventing or alleviating diabetes, or preventing obesity, and foods, drinks, and medicines containing the same. The present invention is accomplished by use of an alpha-amylase inhibitor or an alpha-glucosidase inhibitor as a carbohydrase inhibitor that is extracted from an entire or a part of fagaceous plants using water, another polar solvent, or a mixture thereof. The present invention can also be accomplished by adding the carbohydrase inhibitor to a food or medical composition as an active ingredient for delaying saccharide digestion or absorption, suppressing a rise in postprandial blood glucose levels, or preventing obesity.
Priority: JP20040265281 Applic. Date: 2004-09-13; JP20040381581 Applic. Date: 2004-12-28; WO2005JP10620 Applic. Date: 2005-06-03
Inventor: TSUJITA TAKAHIRO [US]
Application No.: US20070264720A1 Published: 15/Nov/2007Title: Polypropylene binding peptides and methods of use
Applicant/Assignee:
Application No.: 11/607792 Filing Date: 01/Dec/2006
Abstract:Combinatorially generated peptides are provided that have binding affinity for polypropylene (PP). The peptides may be used to deliver benefit agents to various PP surfaces.
Priority: US20050750599P Applic. Date: 2005-12-15
Inventor: CUNNINGHAM SCOTT D [US]; LOWE DAVID J [US]; O'BRIEN JOHN P [US]; WANG HONG [US]; WILKINS ANTOINETTE E [US]
Application No.: US20070265210A1 Published: 15/Nov/2007Title: Administration of C-glycoside compounds for protecting and/or activating gammadeltaT lymphocytes
Applicant/Assignee: L'OREAL
Application No.: 11/783410 Filing Date: 09/Apr/2007
Abstract:C-glycoside compounds having the general formula (I): are useful for protecting and/or stimulating the activity and/or the proliferation of gamma-delta T lymphocyte cells (gammadeltaT cells), and are advantageously formulated into cosmetic/pharmaceutical compositions suited for promoting skin tissue repair, for re-equilibrating epidermal proliferation and differentiation disorders which appear with lack of sleep, and for improving the appearance of the head of hair and limiting hair loss.
Priority: FR20060051269 Applic. Date: 2006-04-07
Inventor: BRETON LIONEL [FR]
Application No.: US20070265253A1 Published: 15/Nov/2007Title: Anti-Inflammatory Compounds
Applicant/Assignee: NEW ZEALAND INSTITUTE FOR CROP & FOOD RESEARCH LIMITED NATIONAL INSTITUTE OF WATER AND ATMOSPHERIC RESEARCH LIMITED MALAGHAN INSTITUTE OF MEDICAL RESEARCH
Application No.: 11/663157 Filing Date: 16/Sep/2005
Abstract:The invention relates to compounds of formula (I) or formula (II) which have anti-inflammatory activity and comprise a new class of NSAIDs. The compounds are therefore useful for treating inflammatory diseases or disorders. The invention also relates to pharmaceutical compositions containing these compounds, as well as methods of treating inflammatory diseases or disorders using compounds of formula (III) or formula (IV).
Priority: NZ20040535383 Applic. Date: 2004-09-17; WO2005NZ00246 Applic. Date: 2005-09-16
Inventor: DENNY WILLIAM A [NZ]; COPP BRENT R [NZ]; PEARCE ALLISON N [NZ]; BERRIDGE MICHAEL V [NZ]; HARPER JACQUIE L [NZ]; PERRY NIGEL B [NZ]; LARSEN LESLEY [NZ]; LARSEN LESLEY [NZ]; GODFREY COLETTE A [AU]
Application No.: US20070265431A1 Published: 15/Nov/2007Title: PMMA binding peptides and methods of use
Applicant/Assignee:
Application No.: 11/607732 Filing Date: 01/Dec/2006
Abstract:Combinatorially generated peptides are provided that have binding affinity for polymethylmethacrylate (PMMA). The peptides may be used to deliver benefit agents to various PMMA surfaces.
Priority: US20050750548P Applic. Date: 2005-12-15
Inventor: CUNNINGHAM SCOTT D [US]; LOWE DAVID J [US]; O'BRIEN JOHN P [US]; WANG HONG [US]; WILKINS ANTOINETTE E [US]
Application No.: US20070269379A1 Published: 22/Nov/2007Title: Penetration Enhancer Combinations for Transdermal Delivery
Applicant/Assignee:
Application No.: 10/560571 Filing Date: 21/Jul/2004
Abstract:A high throughput screening and isolation system identifies rare enhancer mixtures from a candidate pool of penetration enhancer combinations. The combinations are screened for high penetration but low irritation potential using a unique data mining method to find new potent and safe chemical penetration enhancer combinations. The members of a library of chemical penetration enhancer combinations are screened with a high throughput device to identify "hot spots", particular combinations that show higher chemical penetration enhancement compared to neighboring compositions. The irritation potentials of the hot spot combinations are measured to identify combinations that also show low irritation potential. A active component, such as a drug, is then combined with the combination in a formulation which is tested for the ability of the drug to penetrate into or through skin. It is then assessed whether the formulation can deliver the quantity of drug required, and animal tests are conducted to confirm in vivo the ability of the chemical penetration enhancer combinations to facilitate transport of sufficient active molecules across the skin to achieve therapeutic levels of the active molecule in the animal's blood. The invention provides specific unique and rare mixtures of chemical penetration enhancers that enhance skin permeability to hydrophilic macromolecules by more than 50-fold without inducing skin irritation, such as combinations of sodium laurel ether sulfate and 1-phenyl piperazine, and combinations of N-lauryl sarcosine and Span 20/sorbitan monolaurate.
Priority: US20030560717P Applic. Date: 2003-07-23; WO2004US23634 Applic. Date: 2004-07-21
Inventor: MITRAGOTRI SAMIR [US]; KARANDE PANKAJ S [US]; JAIN AMIT K [US]
Application No.: US20070269390A1 Published: 22/Nov/2007Title: OIL-IN-WATER EMULSION
Applicant/Assignee: L'OREAL
Application No.: 11/747998 Filing Date: 14/May/2007
Abstract:Oil-in-water emulsion containing (1) an emulsifying system containing at least one silicone surfactant of molecular weight greater than or equal to 10,000, at least one non-ionic cosurfactant, and at least one anionic cosurfactant, and (2) at least one monohydric alcohol containing from 2 to 6 carbon atoms, where the oils of the oily phase are soluble in the monohydric alcohol. These compositions exhibit good stability and good cosmetic properties. They can be used in many cosmetic and dermatological applications.
Priority: FR20060004406 Applic. Date: 2006-05-17; US20060802505P Applic. Date: 2006-05-23
Inventor: INOUE MIKA [JP]
Application No.: US20070269392A1 Published: 22/Nov/2007Title: Personal care compositions
Applicant/Assignee:
Application No.: 11/801872 Filing Date: 11/May/2007
Abstract:This invention relates to personal care compositions containing polytrimethylene ether glycol in a variety of physical forms including solutions, gels, oil-in-water emulsions, water-in-oil emulsions, suspensions and solids. In a particularly preferred embodiment, the polytrimethylene ether glycol is derived predominantly from monomers obtained from renewable resources, making the personal care products of this embodiment of the present invention more environmentally friendly in terms of their manufacture, use and disposal.
Priority: US20060801166P Applic. Date: 2006-05-17
Inventor: SUNKARA HARI B [US]
Application No.: US20070269393A1 Published: 22/Nov/2007Title: TOPICAL ANESTHETIC FORMULATION
Applicant/Assignee:
Application No.: 11/835500 Filing Date: 08/Aug/2007
Abstract:The topical medicament gel formulation of the present invention includes an anesthetic, an anti-microbial, an oxidant, a nutrient, a diuretic, an opioid, an anti-emetic, an anti-seizure drug, and a non-steroidal anti-inflammatory drug (NSAID), USP in a molecular, as opposed to a salt form, as the active ingredient. Additional constituents illustratively include a skin penetration enhancer and a gelling agent. This invention deals with problems commonly associated with topical application of local medicaments such as: slow onset of action
need for occlusion
and rapid loss of effect due to rapid systemic dispersion. The invention permits enhanced penetration of the medicament and thereby allows for a lesser total dosage of pharmaceutically active ingredient. The use of a lesser total dosage also decreases systemic toxicity.
Priority: US2002-111241 Applic. Date: 2002-07-10; WO2000US41451 Applic. Date: 2000-10-23; US2003-645951 Applic. Date: 2003-08-22
Inventor: WEPFER SCOTT [US]
Application No.: US20070269399A1 Published: 22/Nov/2007Title: HYDROGEN PEROXIDE CONTAINING COMPOSITION
Applicant/Assignee:
Application No.: 11/682374 Filing Date: 06/Mar/2007
Abstract:A hydrogen peroxide containing composition, which sufficiently decreases the stimulation to the scalp, skin, and the like when used as a hair dye. The hydrogen peroxide containing composition includes allantoin, guaiazulene and aloe extract as the second agent for mixing with a first agent containing an oxidation dye. These ingredients in the hydrogen peroxide containing composition act synergistically and demonstrate an anti-inflammatory effect, an anti-allergic action, and a moisture retention effect.
Priority: JP20060137879 Applic. Date: 2006-05-17
Inventor: TAGAWA SADAO [JP]
Application No.: US20070269405A1 Published: 22/Nov/2007Title: Androgen Receptor Modulators
Applicant/Assignee: MERCK & CO., INC
Application No.: 11/660289 Filing Date: 19/Aug/2005
Abstract:Compounds of structural Formula (I) are modulators of the androgen receptor (AR) in a tissue selective manner These compounds are useful in the enhancement of weakened muscle tone and the treatment of conditions caused by androgen deficiency or which can be ameliorated by androgen administration, including osteoporosis, osteopenia, glucocorticoid-induced osteoporosis, periodontal disease, bone fracture, bone damage following bone reconstructive surgery, sarcopenia, frailty, aging skin, male hypogonadism, postmenopausal symptoms in women, atherosclerosis, hypercholesterolemia, hyperlipidemia, obesity, aplastic anemia and other hematopoietic disorders, inflammatory arthritis and joint repair, HIV-wasting, prostate cancer, benign prostatic hyperplasia (BPH), abdominal adiposity, metabolic syndrome, type II diabetes, cancer cachexia, Alzheimer's disease, muscular dystrophies,
cognitive decline, sexual dysfunction, sleep apnea, depression, premature ovarian failure, and autoimmune disease, alone or in combination with other active agents.
Priority: US20040604368P Applic. Date: 2004-08-25; WO2005US29592 Applic. Date: 2005-08-19
Inventor: WANG JIABING [US]; CLOSE JOSHUA [US]
Application No.: US20070269473A1 Published: 22/Nov/2007Title: Microbial Encapsulation
Applicant/Assignee: MICAP PLC
Application No.: 11/587746 Filing Date: 07/Aug/2007
Abstract:The present invention relates to a method of encapsulation and a composition comprising an encapsulate material.
Priority: GB20040009374 Applic. Date: 2004-04-27; GB20040021590 Applic. Date: 2004-09-29; WO2005GB01604 Applic. Date: 2005-04-27
Inventor: NELSON GORDON [GB]
Application No.: US20070269524A1 Published: 22/Nov/2007Title: Use of Idrocilamide for the Preparation of a Pharmaceutical Composition of Rosacea
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT, S.N.C
Application No.: 10/580251 Filing Date: 10/Nov/2004
Abstract:The invention relates to the use of idrocilamide for the preparation of novel pharmaceutical compositions, more particularly dermatological compositions, which can be used to treat rosacea.
Priority: FR20030013666 Applic. Date: 2003-11-21; WO2004FR02899 Applic. Date: 2004-11-10
Inventor: DOLFI FABRIZIO [FR]; PILGRIM WILLIAM R [FR]
Application No.: US20070269526A1 Published: 22/Nov/2007Title: Carotenoid Composition and Method for Preparation Thereof
Applicant/Assignee:
Application No.: 11/576276 Filing Date: 29/Sep/2005
Abstract:This invention relates to a carotenoid composition comprising the carotenoid as particles of size smaller than 100 nanometers in an oil medium and a method of preparing the composition by milling the carotenoid in an oil medium and therapeutic compositions containing the carotenoid.
Priority: AU20040905670 Applic. Date: 2004-09-29; WO2005AU01515 Applic. Date: 2005-09-29
Inventor: BOS MICHAEL A [AU]; ELLIS DAVID G [AU]
Application No.: US20070269534A1 Published: 22/Nov/2007Title: Methods of treating skin to enhance therapeutic treatment thereof
Applicant/Assignee:
Application No.: 11/645405 Filing Date: 26/Dec/2006
Abstract:Excellent percutaneous absorption of drug or active agent is achieved by pre-treating skin with a cationic constituent prior to application of a drug or active agent.
Priority: US20060764410P Applic. Date: 2006-02-02
Inventor: RAMIREZ JOSE E [US]; FARYNIARZ JOSEPH [US]
Application No.: US20070269537A1 Published: 22/Nov/2007Title: Skin Condition Improvement Including Acne, Rosacea, and Topical Wounds by Artemisia Annua Extract via Iron Siderophore Trojan Horse Delivery System
Applicant/Assignee: BIODERM RESEARCH
Application No.: 11/615561 Filing Date: 01/Jan/2007
Abstract:This invention relates to certain extracts of Artemisia annua plant, both in their crude and refined forms, and certain refined forms of Artemisia annua plant extracts composed substantially of Artemisinin and its analogs, which are chemically classified as sesquiterpenes with an endo-peroxide group [FIG. 1 ]. These are suitable for compositions comprising topical application, and for the treatment or improvement of skin condition including acne, rosacea, topical wounds, age spots, wrinkles, excess facial oil, and darkened skin.
Priority: US2003-248691 Applic. Date: 2003-02-10
Inventor: GUPTA SHYAM K [US]
Application No.: US20070270340A1 Published: 22/Nov/2007Title: ADP-ribosyl transferase fusion variant proteins
Applicant/Assignee:
Application No.: 11/643940 Filing Date: 22/Dec/2006
Abstract:The present invention relates to novel chimeric C3-like Rho antagonists and their use for promoting repair and neuron survival in injured mammalian central and peripheral nervous system and for treating or preventing cancer.
Priority: CA20012342970 Applic. Date: 2001-04-12; CA20012362004 Applic. Date: 2001-11-13; CA20022367636 Applic. Date: 2002-01-15; US2004-902878 Applic. Date: 2004-08-02; US2004-902959 Applic. Date: 2004-08-02; US20030506162P Applic. Date: 2003-09-29
Inventor: MCKERRACHER LISA [CA]; MUNZER JON S [CA]
Application No.: US20070270370A1 Published: 22/Nov/2007Title: Novel bicyclonucleoside analogues
Applicant/Assignee: SANKYO COMPANY, LIMITED
Application No.: 11/700361 Filing Date: 31/Jan/2007
Abstract:Oligonucleotide analogues which have anti-sense or anti-gene activity, as well as in vivo stability, or pharmaceutically acceptable salts thereof. The oligonucleotide analogues have one or more structural units represented by the following formula (1a): provided that when the oligonucleotide has two or more structural units of formula (1a), each B is the same or different, wherein B represents a purin-9-yl group or a 2-oxo-1,2-dihydropyrimidin-1-yl group.
Priority: JP19990207170 Applic. Date: 1999-07-22; US2002-054300 Applic. Date: 2002-01-22; WO2000JP04902 Applic. Date: 2000-07-21
Inventor: IMANISHI TAKESHI [JP]; OBIKA SATOSHI [JP]
Application No.: US20070270382A1 Published: 22/Nov/2007Title: Composition for Protecting Skin
Applicant/Assignee:
Application No.: 10/574275 Filing Date: 01/Oct/2004
Abstract:Disclosed are a composition for protecting skin and uses thereof. The composition comprises sphingomyelin as an active ingredient and protects the skin by inhibiting skin aging, treating a skin wound and improving a skin barrier.
Priority: KR20030068932 Applic. Date: 2003-10-02; KR20040075864 Applic. Date: 2004-09-22; WO2004KR02517 Applic. Date: 2004-10-01
Inventor: PARK CHANGSEO [KR]; KIM SUNKI [KR]; KIM JINWOOK [KR]; KANG HYEONGJOON [KR]; HAN BOKYUNG [KR]; LEE YOUNGGON [KR]; CHUNG SOYOUNG [KR]; CHOI WANGKEUN [KR]; NAM SANG J [KR]
Application No.: US20070270496A1 Published: 22/Nov/2007Title: Pharmaceutical composition for the treatment of pathologies caused by the general response of the immune system
Applicant/Assignee: EPITECH GROUP S.R.L
Application No.: 11/724501 Filing Date: 14/Mar/2007
Abstract:The present invention relates to a pharmaceutical composition consisting of amides of mono- and di-carboxylic acids and hydroxystilbenes, and may be used for the treatment of pathologies caused, sustained and/or characterised by an abnormal general response of the immune system, in both humans and animals.
Priority: EP20060425206 Applic. Date: 2006-03-28
Inventor: DELLA VALLE FRANCESCO [IT]; DELLA VALLE MARIA F [IT]; MARCOLONGO GABRIELE [IT]; RAVAGNAN GIANPIERO [IT]; DI MARZO VINCENZO [IT]
Application No.: US20070270738A1 Published: 22/Nov/2007Title: Method of treating ACNE with stratum corneum piercing patch
Applicant/Assignee:
Application No.: 11/690960 Filing Date: 26/Mar/2007
Abstract:The invention features a method of treating acne by piercing the stratum corneum of skin in need of such treatment with a stratum corneum-piercing device that contains at least one stratum corneum-piercing microprotrusion and a compressible cover such that the compressible cover substantially encases the at least one stratum corneum-piercing microprotrusion, and wherein upon contacting the skin with the compressible cover, the at least one stratum corneum-piercing microprotrusion protrudes from the compressible cover and pierces the stratum corneum of the skin.
Priority: US2006-409454 Applic. Date: 2006-04-21; US2005-113890 Applic. Date: 2005-04-25
Inventor: WU JEFFREY M [US]; LIU JUE C [US]; SUN YING [US]; MCDONOUGH JUSTIN [US]; LAMBINO DANILO [AU]; MAGHRIBI MARIAM [US]
Application No.: US20070271709A1 Published: 29/Nov/2007Title: Method and composition for avoiding staining during hair coloring
Applicant/Assignee:
Application No.: 11/786429 Filing Date: 11/Apr/2007
Abstract:A compound or mixture and a method are provided for preventing the coloring of hair or skin during a coloring procedure. The system may include two components: a compound that chemically protects the surface of the hair to which it is applied
and an applicator to accurately apply the compound to a region of the hair or skin that is desired to not be subject to the coloration procedure, in other words, to not be colored.
Priority: US20060791000P Applic. Date: 2006-04-11
Inventor: KING RICHARD [US]
Application No.: US20070274932A1 Published: 29/Nov/2007Title: Water in oil emulsion compositions containing sunscreen actives and siloxane elastomers
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/803534 Filing Date: 15/May/2007
Abstract:The present invention relates to water in oil emulsion compositions suitable for use as sunscreen comprising: from about 0.1% to about 15% of an emulsifying crosslinked siloxane elastomer
from about 1% to about 40% of a solvent for the emulsifying crosslinked siloxane elastomer
from about 0.01% to about 5% of an additional emulsifier
from about 50% to about 99% of aqueous phase
and from about 0.01% to about 30% of a sunscreen active
wherein when shear stress is applied to the composition during spreading on skin, aqueous phase is released from the emulsion.
Priority: US20060800554P Applic. Date: 2006-05-15; US20060812791P Applic. Date: 2006-06-12
Inventor: SUGINAKA YASUKO [JP]; TANAKA HIDEKAZU [JP]; YOSHIMI NAOHISA [JP]
Application No.: US20070274934A1 Published: 29/Nov/2007Title: Bis-urea compounds and compositions and method of cosmetic treatment
Applicant/Assignee:
Application No.: 11/797931 Filing Date: 09/May/2007
Abstract:Disclosed herein is a cosmetic and/or pharmaceutical composition comprising, in a physiologically acceptable medium, a fatty phase and at least one compound chosen from compounds of formula (I), salts thereof, and isomers thereof, used to texture the fatty phase. Also disclosed herein is a method for texturing a cosmetic and/or pharmaceutical composition comprising adding to the composition at least one compound of formula (I). Further disclosed herein is a method for the cosmetic treatment of keratin materials comprising applying to the materials at least one composition of the present disclosure.
Priority: FR20060051653 Applic. Date: 2006-05-09; US20060802108P Applic. Date: 2006-05-22
Inventor: CHODOROWSKI-KIMMES SANDRINE [FR]
Application No.: US20070274936A1 Published: 29/Nov/2007Title: Oligonucleotide and the Use Thereof for Modulating an Isoform C Beta-1 Protein-Kinase in the Form of a Skin Depigmentation Agent
Applicant/Assignee:
Application No.: 10/584982 Filing Date: 28/Dec/2004
Abstract:This invention relates to oligonucleotide sequences and their derivatives. These oligonucleotide sequences are capable of hybridising with the genes or with products of the genes coding for the PKC-beta 1. This invention also relates to the use of these oligonucleotide sequences as a depigmenting or bleaching agent for the skin in a cosmetic composition or in a topical pharmaceutical composition.
Priority: FR20030015560 Applic. Date: 2003-12-30; WO2004FR03397 Applic. Date: 2004-12-28
Inventor: KURFURST ROBIN [FR]; NIZARD CARINE [FR]
Application No.: US20070274937A1 Published: 29/Nov/2007Title: Use of a Cruciferous Protein Hydrolysate as a Depigmentation Agent or For a Cosmetic and/or Pharmaceutical Composition
Applicant/Assignee:
Application No.: 11/578507 Filing Date: 21/Apr/2005
Abstract:A composition and method for whitening and/or depigmenting skin with a protein hydrolysate from plants belonging to the crucifer family.
Priority: FR20040004192 Applic. Date: 2004-04-21; WO2005FR00985 Applic. Date: 2005-04-21
Inventor: DAL FARRA CLAUDE [FR]; DOMLOGE NOUHA [FR]; PEYRONEL DOMINIQUE [FR]
Application No.: US20070274988A1 Published: 29/Nov/2007Title: Kiaa0779, Splice Variants Thereof, and Methods of Their Use
Applicant/Assignee: FIVE PRIME THERAPEAUTICS, INC
Application No.: 10/575265 Filing Date: 12/Oct/2004
Abstract:The invention provides novel polynucleotides, related polypeptides related nucleic acid and polypeptide compositions, and related modulators, such as antibodies and small molecule modulators. The invention also provides methods to make and use these polynucleotides, polypeptides, related compositions, and modulators. These methods include diagnostic, prophylactic, and therapeutic applications. The compositions and methods of the invention are useful in treating proliferative disorders, e.g., cancers, such as kidney and pancreatic cancer
and inflammatory, immune, and viral disorders.
Priority: US20030510612P Applic. Date: 2003-10-10; WO2004US33408 Applic. Date: 2004-10-12
Inventor: WONG JUSTIN G [US]; HESTIR KEVIN [US]; COLLINS AMY L T [US]; LEE ERNESTINE [US]
Application No.: US20070275070A1 Published: 29/Nov/2007Title: Barrier film-forming germicidal composition for controlling mastitis
Applicant/Assignee:
Application No.: 11/439941 Filing Date: 24/May/2006
Abstract:A long-lasting persistent, uniform film-forming skin protecting germicidal composition provides a long-lasting persistent barrier film when applied to skin. The compositions have particular utility as barrier teat dips for protecting cows against mastitis. A barrier film-forming agent is selected from the modified or hydrolyzed polysaccharides, particularly a hydrolyzed or modified starch, such as dextrin and maltodextrin. The barrier film-forming agent is stably solubilized in a solvent that dries to form the long-lasting persistent uniform film over the animal skin. The compositions also contain antimicrobial agents that fight against microbes that manage to penetrate the protective barrier film. Particularly, advantageous is that all the materials used are safe food additive and cost effective over the traditional barrier film forming agents.
Priority:
Inventor: AHMED FAHIM U [US]; TRAISTARU N CAMELIA [US]; UYTTERHAEGEN LIEVEN [BE]
Application No.: US20070275073A1 Published: 29/Nov/2007Title: Clay-based hemostatic agents and devices for the delivery thereof
Applicant/Assignee: Z-MEDICA CORPORATION
Application No.: 11/590427 Filing Date: 30/Oct/2006
Abstract:A device for promoting the clotting of blood comprises a clay material in particle form and a receptacle for containing the clay material. At least a portion of the receptacle is defined by a mesh. Another device comprises a gauze substrate and a clay material disposed on the gauze substrate. Another device is a bandage comprising a substrate, a mesh mounted on the substrate, and particles of a clay material retained in the mesh. A hemostatic sponge comprises a substrate, a hemostatic material disposed on a first surface of the substrate, and a release agent disposed on a second surface of the substrate. The release agent is disposed on the wound-contacting surface of the substrate. When treating a bleeding wound, application of the hemostatic sponge causes at least a portion of the hemostatic material to come into contact with blood through the release agent and through the substrate.
Priority: US20060808618P Applic. Date: 2006-05-26; US20060810447P Applic. Date: 2006-06-01
Inventor: HUEY RAYMOND [US]; LO DENNY [US]; BURNS DANIEL J [US]
Application No.: US20070275929A1 Published: 29/Nov/2007Title: Composition and method for controlling the transmission of noroviruses
Applicant/Assignee: THE DIAL CORPORATION
Application No.: 11/805296 Filing Date: 23/May/2007
Abstract:Antimicrobial compositions having a rapid effectiveness against noroviruses and against bacteria are disclosed. The antimicrobial compositions contain a disinfecting alcohol, an organic acid, and water, wherein the composition has a pH of about 5 or less and the nonvolatile components of the composition are capable of forming a barrier film or layer on a treated surface.
Priority: US20060811354P Applic. Date: 2006-06-06; US20060802911P Applic. Date: 2006-05-24
Inventor: FULS JANICE L [US]; RODGERS NANCY D [US]; THEILER RICHARD F [US]; PEDERSEN DANIEL E [US]; MOLINARO KATHERINE J [US]; ROLANDO JOHN J [US]
Application No.: US20070275943A1 Published: 29/Nov/2007Title: Method and Composition for Treatment or Prophylaxis of Amyloidosis Disorders
Applicant/Assignee: ACRUX DDS PTY LTD
Application No.: 10/579754 Filing Date: 19/Nov/2004
Abstract:A method of treatment or prophylaxis of amyloidosis disorders in a patient the method comprising topically applying to an area of skin of the patient a composition comprising: one or more zinc chelators
and one or more dermal penetration enhancers.
Priority: US20030523139P Applic. Date: 2003-11-19; WO2004AU01610 Applic. Date: 2004-11-19
Inventor: MORGAN TIMOTHY M [AU]; WILKINS NINA F [AU]
Application No.: US20070275955A1 Published: 29/Nov/2007Title: METHOD OF TREATING TUMORS
Applicant/Assignee: ED. GEISTLICH SOEHNE AG
Application No.: 11/670760 Filing Date: 02/Feb/2007
Abstract:A method of treatment for preventing or reducing tumor growth in a patient includes administering to the patient an effective about of taurolidine, taurultam or a mixture thereof, so as to prevent or reduce the tumor growth in the patient.
Priority: US20010281713P Applic. Date: 2001-04-06; US20010284933P Applic. Date: 2001-04-20; US20010284934P Applic. Date: 2001-04-20; GB19970016219 Applic. Date: 1997-07-31; US2006-351262 Applic. Date: 2006-02-10; US2001-971774 Applic. Date: 2001-10-09; US2000-493797 Applic. Date: 2000-01-28; WO1998GB02311 Applic. Date: 1998-07-31; US2003-424102 Applic. Date: 2003-04-28; US2002-281138 Applic. Date: 2002-10-28; US2000-583902 Applic. Date: 2000-06-01; US2004-934474 Applic. Date: 2004-09-07; US2002-109058 Applic. Date: 2002-03-29; US19990137421P Applic. Date: 1999-06-04; US19990151050P Applic. Date: 1999-08-27; US19990167681P Applic. Date: 1999-11-29; US20000174607P Applic. Date: 2000-01-05; US20000182200P Applic. Date: 2000-02-14; US20010280748P Applic. Date: 2001-04-03; US20010281710P Applic. Date: 2001-04-06; US20010281711P Applic. Date: 2001-04-06; US20010281712P Applic. Date: 2001-04-06
Inventor: PFIRRMANN ROLF W [CH]
Application No.: US20070275962A1 Published: 29/Nov/2007Title: Heterobicyclic Compounds as Pharmaceutically Active Agents
Applicant/Assignee: GPC BIOTECH AG
Application No.: 10/597120 Filing Date: 10/Sep/2004
Abstract:Described are heterobicyclic compounds such as 4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid amides, 4,7-dihydro-5H-thieno[2,3-c]thiopyran 3-carboxylic acid amides, 4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid amides, or benzo[b]thiophene-3-carboxylic acid amides and pharmaceutically acceptable salts thereof, the use of these derivatives for the prophylaxis and/or treatment of various diseases such as infectious diseases, including mycobacteriainduced infections and opportunistic diseases, prion diseases, immunological diseases, autoimmune diseases, bipolar and clinical disorders, cardiovascular diseases, cell proliferative diseases, diabetes, inflammation, transplant rejections, erectile dysfunction, neurodegenerative diseases and stroke, as well as compositions containing at least one heterobicyclic compound and/or pharmaceutically acceptable salts thereof. Furthermore, reaction procedures for the synthesis of the heterobicyclic compound are disclosed.
Priority: EP20040012814 Applic. Date: 2004-05-28; EP20030020616 Applic. Date: 2003-09-10; EP20040004891 Applic. Date: 2004-03-02; US20030502606P Applic. Date: 2003-09-15; US20040551341P Applic. Date: 2004-03-10; US20040577043P Applic. Date: 2004-06-07; WO2004EP10161 Applic. Date: 2004-09-10
Inventor: KOUL ANIL [BE]; KLEBL BERT [DE]; MULLER GERHARD [DE]; MISSIO ANDREA [IT]; SCHWAB WILFRIED [DE]; HAFENBRADL DORIS [DE]; NEUMANN LARS [DE]; SOMMER MARC-NICOLA [DE]; MULLER STEFAN [DE]; HOPPE EDMUND [DE]; FREISLEBEN ACHIM [DE]; BACKES ALEXANDER [DE]; HARTUNG CHRISTIAN [DE]; FELBER BEATRICE [DE]; ZECH BIRGIT [DE]; ENGKVIST OLA [SE]; KERI GYORGY [HU]; ORFI LASZLO [HU]; BANHEGYI PETER [HU]; GREFF ZOLTAN [HU]; HORVATH ZOLTAN [HU]; VARGA ZOLTAN [HU]; MARKO PETER [HU]; PATO JANOS [HU]; SZABADKAI ISTVAN [HU]; SZEKELYHID ZSOLT [HU]; WACZEK FRIGYES [HU]
Application No.: US20070275968A1 Published: 29/Nov/2007Title: Substituted Biphenyl Derivative
Applicant/Assignee:
Application No.: 11/574811 Filing Date: 05/Sep/2005
Abstract:The present invention relates to a biaryl derivative or a pharmacologically acceptable salt thereof having an excellent collagen-synthesis inhibition activity. A biaryl derivative having a structure represented by the following General Formula (I) or a pharmacologically acceptable salt thereof: wherein R<1 >represents a C6-C10 aryl group which is substituted with one to three group(s) each independently selected from the group consisting of a group defined by formula R-L-, a di-(C1-C6 alkyl)amino group, a di-(C1-C6 alkyl)aminosulfonyl group, a hydroxyaminocarbonyl group, and a halogen atom, and so on
R represents a C1-C6 alkyl group, and so on
L represents a sulfonyl group, an aminosulfonyl group, or a sulfonylamino group, and so on
R<2 >represents a hydrogen atom, and so on
A represents a group defined by formula (II), (III), or (IV)
R<3 >represents a C1-C6 alkyl group, and so on
and R<4 >represents a C1-C6 alkyl group, and so on.
Priority: JP20040259535 Applic. Date: 2004-09-07; WO2005JP16212 Applic. Date: 2005-09-05
Inventor: KURATA HITOSHI [JP]; NISHIMATA TOYOKI [JP]; WATANABE YUKIKO [JP]; EBISAWA MASAYUKI [JP]; FUJIMOTO TEPPEI [JP]; KOBAYASHI HIDEKI [JP]
Application No.: US20070275978A1 Published: 29/Nov/2007Title: Of at Use of an Antagonist Compound of at Least One Receptor Selected From a Group Comprising Beta-Adrenergic Receptors, A at1, 5-Ht5 and Galanin Receptor for Preparing a Pharmaceutical Composition for Treating Rosacea
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT S.N.C
Application No.: 10/590077 Filing Date: 17/Feb/2005
Abstract:The invention relates to the use of an antagonist of at least one receptor chosen from the group comprising the beta-adrenergic receptors, the AT1 receptor, the 5-HT2 receptor, the 5-HT5 receptor and the galanin receptor, for the preparation of a pharmaceutical composition for treating rosacea.
Priority: FR20040001715 Applic. Date: 2004-02-20; WO2005FR00367 Applic. Date: 2005-02-17
Inventor: DOLFI FABRIZIO [FR]; SAFONOVA IRINA [FR]
Application No.: US20070276000A1 Published: 29/Nov/2007Title: CHEMICAL COMPOUNDS
Applicant/Assignee: GLAXO SMITH KLINE LLC
Application No.: 11/570838 Filing Date: 21/Jun/2005
Abstract:The present invention relates to cycloalkylidene compounds with a variety of therapeutic uses, more particularly novel naphthalene compounds that are particularly useful for selective estrogen modulation.
Priority: WO2005US21963 Applic. Date: 2005-06-21; US20040581913P Applic. Date: 2004-06-22
Inventor: HEYER DENNIS [US]; FANG JING [US]; NAVAS III FRANK [US]; KATAMREDDY SUBBA R [US]; PECKHAM JENNIFER P [US]; TURNBULL PHILIP S [US]; MILLER AARON B [US]; AKWABI-AMEYAN ADWOA [US]; DADSWELL CHARLES E [US]
Application No.: US20070276345A1 Published: 29/Nov/2007Title: Clay-based hemostatic agents and devices for the delivery thereof
Applicant/Assignee: Z-MEDICA CORPORATION
Application No.: 11/715057 Filing Date: 06/Mar/2007
Abstract:A hemostatic device for promoting the clotting of blood includes a gauze substrate, a clay material disposed on the gauze substrate, and also a polyol such as glycerol or the like disposed on the gauze substrate to bind the clay material. When the device is used to treat a bleeding wound, at least a portion of the clay material comes into contact with blood emanating from the wound to cause the clotting. A bandage that can be applied to a bleeding wound to promote the clotting of blood includes a flexible substrate and a gauze substrate mounted thereon. The gauze substrate includes a clay material and a polyol. A hemostatic sponge also includes a gauze substrate and a dispersion of hemostatic material and a polyol on a first surface of the substrate.
Priority: US2006-590427 Applic. Date: 2006-10-30; US20060808618P Applic. Date: 2006-05-26; US20060810447P Applic. Date: 2006-06-01
Inventor: HUEY RAYMOND [US]; LO DENNY [US]; BURNS DANIEL J [US]
Application No.: US20070280317A1 Published: 06/Dec/2007Title: COMPOSITE LASER ROD,FABRICATING METHOD THEREOF, AND LASER DEVICE THEREWITH
Applicant/Assignee: KONOSHIMA CHEMICAL CO. LTD
Application No.: 11/561301 Filing Date: 17/Nov/2006
Abstract:As a composite laser rod capable of satisfying the positional stability and output stability of a laser beam, a laser rod in which a laser active element is doped is intimately inserted into a hollow portion of a non-doped ceramic pipe that has a crystal structure the same as the laser rod followed by baking so as to remove a gap and strain at an interface between the laser rod and the ceramic pipe after the baking further followed by polishing a surface of the ceramic pipe to form a ceramic skin layer, and thereby a composite laser rod is formed. In the composite laser rod, an influence due to fluctuation in the cooling capacity of cooling water or a heat sink is averaged by a non-doped skin layer, temperature fluctuation of the laser rod is suppressed, and an influence of vibration from the cooling water or a cooling fan can be suppressed.
When the refractive index of the laser rod is made higher than that of the ceramic pipe, a high efficiency oscillation can be realized, and furthermore when the thermal conductivity of the ceramic pipe is made higher than that of the laser rod, the thermal lens effect can be alleviated.
Priority: JP20020051360 Applic. Date: 2002-02-27; US2003-372836 Applic. Date: 2003-02-26
Inventor: KOUTA HIKARU [JP]; SUZUKI YOSHIKAZU [JP]; KUDO SHUETSU [JP]; TSUNEKANE MASAKI [JP]; MUKAIHARA KATSUJI [JP]; YANAGITANI TAKAGIMI [JP]; YAGI HIDEKI [JP]
Application No.: US20070280891A1 Published: 06/Dec/2007Title: Oleaginous pharmaceutical and cosmetic foam
Applicant/Assignee: FOAMIX LTD
Application No.: 11/645444 Filing Date: 26/Dec/2006
Abstract:The invention relates to stable oleaginous cosmetic or therapeutic foam compositions containing certain active agents, having unique therapeutic properties and methods of treatment using such compositions. The foamable composition includes a polyethylene glycol (PEG) or PEG derivative and mixtures thereof, wherein the PEG or PEG derivative is present at a concentration of about 70% to about 96.5% by weight of the total composition
a surface-active agent at a concentration of about 0.1% to less than about 10% by weight of the total composition
and a therapeutically effective amount of at least one active agent.
Priority: US2004-835505 Applic. Date: 2004-04-28; US20030530015P Applic. Date: 2003-12-16; US20030492385P Applic. Date: 2003-08-04
Inventor: TAMARKIN DOV [IL]; FRIEDMAN DORON [IL]; EINI MEIR [IL]; BESONOV ALEX [IL]
Application No.: US20070280900A1 Published: 06/Dec/2007Title: Compositions having a high antiviral efficacy
Applicant/Assignee: THE DIAL CORPORATION
Application No.: 11/807457 Filing Date: 29/May/2007
Abstract:Antiviral compositions having a rapid antiviral effectiveness, and a persistent antiviral effectiveness, are disclosed. The antimicrobial compositions contain (a) a powdered solid substrate and (b) an organic acid.
Priority: US20060809291P Applic. Date: 2006-05-30; US20060811354P Applic. Date: 2006-06-06
Inventor: FOX PRISCILLA S [US]; PEDERSEN DANIEL E [US]; ROLANDO JOHN J [US]; STAUB RICHARD K [US]
Application No.: US20070280901A1 Published: 06/Dec/2007Title: Method of inhibiting the transmission of influenza virus
Applicant/Assignee: THE DIAL CORPORATION
Application No.: 11/809068 Filing Date: 31/May/2007
Abstract:Antimicrobial compositions having a rapid and persistent antiviral effectiveness against influenza viruses, including avian flu viruses, are disclosed. The antimicrobial compositions contain (a) a disinfecting alcohol, (b) an organic acid, and (c) water, wherein the composition has a pH of about 5 or less and the nonvolatile components of the composition are capable of forming a barrier film or layer on a treated surface.
Priority: US20060810389P Applic. Date: 2006-06-02; US20060811354P Applic. Date: 2006-06-06
Inventor: FULS JANICE L [US]; RODGERS NANCY D [US]; THEILER RICHARD F [US]; PEDERSEN DANIEL E [US]; ROLANDO JOHN J [US]; STAUB RICHARD K [US]
Application No.: US20070280999A1 Published: 06/Dec/2007Title: ORALLY ADMINISTRABLE COMPOSITION FOR THE PHOTOPROTECTION OF THE SKIN
Applicant/Assignee: NESTEC S.A
Application No.: 11/772704 Filing Date: 02/Jul/2007
Abstract:An orally administrable composition for the photoprotection of the skin which comprises the combination of i) at least one probiotic lactic acid bacterium or a culture supernatant thereof, and ii) at least one carotenoid or derivative, included into an orally acceptable carrier.
Priority: EP20020075703 Applic. Date: 2002-02-21; US2004-505305 Applic. Date: 2004-10-27; WO2003EP01685 Applic. Date: 2003-02-18
Inventor: BRETON LIONEL [FR]; BUREAU-FRANZ ISABELLE [CH]; FANCHON CHANTAL [FR]
Application No.: US20070281037A1 Published: 11/May/2006Title: Sterile preparations and compositions including stinging capsules and methods of producing and using same
Applicant/Assignee: NANOCYTE INC
Application No.: 10/981522 Filing Date: 05/Nov/2004
Abstract:A sterile stinging capsule preparation and methods of producing and using same are provided.
Priority: US2004-868802 Applic. Date: 2004-06-17; US2003-406202 Applic. Date: 2003-04-04; US2001-963672 Applic. Date: 2001-09-27; US20000235910P Applic. Date: 2000-09-28
Inventor: LOTAN TAMAR [IL]
Application No.: US20070281047A1 Published: 06/Dec/2007Title: Composition Containing a Plant Extract and Process for Producing Same
Applicant/Assignee: COGNIS FRANCE, S.A.S
Application No.: 10/576816 Filing Date: 15/Oct/2004
Abstract:A composition which includes a pulp extract from the fruit of Argania spinosa and at least one dermopharmaceutical or cosmetic auxiliary and/or additive is provided. A process for producing an extract from the fruit of Argania spinosa, and a triterpene fraction of an extract of the pulp of the fruit of Argania spinosa including lupeol, alpha-amyrine, beta-amyrine, taraxasterol, and psi-taraxasterol are also provided.
Priority: EP20030292668 Applic. Date: 2003-10-24; WO2004EP11625 Applic. Date: 2004-10-15
Inventor: HENRY FLORENCE [FR]; DANOUX LOUIS [FR]; PAULY GILLES [FR]
Application No.: US20070281984A1 Published: 06/Dec/2007Title: Use Of Metronidazole For Preparing A Pharmaceutical Composition For Treating A Cutaneous Inflammation
Applicant/Assignee: GALDERMA RESEARCH & DEVELOPMENT, S.N.C
Application No.: 10/590078 Filing Date: 17/Feb/2005
Abstract:The invention relates to use of metronidazole for the preparation of a pharmaceutical composition for treating cutaneous inflammation, and preferentially the inflammatory component of rosacea.
Priority: FR20040001723 Applic. Date: 2004-02-20; WO2005FR00371 Applic. Date: 2005-02-17
Inventor: DOLFI FABRIZIO [FR]; SAFONOVA IRINA [FR]
Application No.: US20070281999A1 Published: 06/Dec/2007Title: Alcohol-containing antimicrobial compositions having improved efficacy
Applicant/Assignee: THE DIAL CORPORATION
Application No.: 11/807689 Filing Date: 30/May/2007
Abstract:Antimicrobial compositions having a rapid antiviral and antibacterial effectiveness, and a persistent antiviral effectiveness, are disclosed. The antimicrobial compositions contain (a) a disinfecting alcohol, (b) a blend containing a C12 to C22 alcohol and an ethoxylated C12 to C22 alcohol, such as a cetearyl alcohol and cetereth-20 blend, a cetearyl alcohol, steareth-20, and steareth-10 blend, or a mixture thereof, (c) an optional organic acid, and (c) water.
Priority: US20060811354P Applic. Date: 2006-06-06; US20060809495P Applic. Date: 2006-05-31
Inventor: FOX PRISCILLA S [US]; PEDERSEN DANIEL E [US]; ROLANDO JOHN J [US]; STAUB RICHARD K [US]
Application No.: US20070283516A1 Published: 13/Dec/2007Title: Disposable nonwoven implement
Applicant/Assignee: THE IAMS COMPANY
Application No.: 11/788410 Filing Date: 20/Apr/2007
Abstract:A disposable nonwoven implement that is retained on a user's hand during use is provided. The disposable nonwoven implement can be associated with a composition.
Priority: US20060794701P Applic. Date: 2006-04-25
Inventor: RASMUSSEN CRAIG MERILLAT [US]; MASON BRENT WILLIAM [US]; SCHULLER DAVID WILLIAM [US]; CAUDILL SHELLIE JEAN PORTER [US]
Application No.: US20070283977A1 Published: 13/Dec/2007Title: Composition comprising novel polyurethanes and cosmetic treatment process
Applicant/Assignee:
Application No.: 11/723455 Filing Date: 20/Mar/2007
Abstract:The present disclosure relates to novel polyurethanes comprising cationic units, of diisocyanates and of nonionic units derived from polyolefins comprising at least 10 mol % of units comprising at least one residual carbon-carbon double bond. The present disclosure also relates to cosmetic or pharmaceutical compositions comprising the polyurethanes, and also to a cosmetic treatment process, for example for shaping and/or holding the hair, comprising the application of such a composition.
Priority: FR20060050951 Applic. Date: 2006-03-20; US20060785988P Applic. Date: 2006-03-27
Inventor: MOUGIN NATHALIE [FR]; SCHULTZE XAVIER [FR]
Application No.: US20070286669A1 Published: 13/Dec/2007Title: Kit for the application of a fluid preparation
Applicant/Assignee: BEIERSDORF AG
Application No.: 11/447949 Filing Date: 07/Jun/2006
Abstract:A kit for applying a fluid onto a surface. The kit comprises (i) a fluid having a yield point, (ii) a container having at least one opening, and (iii) an applicator for applying the fluid to a surface. The applicator comprises a porous area, whereby when the applicator is disposed on the opening of the container and the porous area is in contact with the fluid, the fluid wets the porous area of the applicator without leaking out of it, as long as the porous area is not in contact with the surface. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
Priority:
Inventor: NUEBEL THOMAS [DE]; BIEL STEFAN [DE]
Application No.: US20070286824A1 Published: 13/Dec/2007Title: Bleed-resistant colored microparticles and skin care compositions comprising them
Applicant/Assignee:
Application No.: 11/448353 Filing Date: 07/Jun/2006
Abstract:Bleed-resistant microparticles comprising at least one colorant, a process to produce them, compositions containing them and their use in skin care applications to produce a natural, textured tone effect.
Priority:
Inventor: RABE THOMAS ELLIOT [US]; WILDGUST PAUL GRAHAM [US]; MORRISSEY CHRISTOPHER TODD [US]; JONES STEPHEN RAY [US]; GREY BRYAN DAVID [GB]; DYMOND PAUL MICHAEL [GB]; BAXTER MARK CHRISTOPHER [GB]; ANDRIANOV CHRISTINA LIGIA [US]
Application No.: US20070286829A1 Published: 13/Dec/2007Title: Antiperspirant Or Deodorant Compositions
Applicant/Assignee:
Application No.: 11/596451 Filing Date: 03/May/2005
Abstract:The stability of antiperspirant or deodorant compositions comprising an aqueous solution of an antiperspirant or deodorant salt that has been thickened by a polyquaternium derivative of an hydroxycellulose and containing lypophylic organic material can be improved by employing a stabilising amount of propylene glycol, preferably selected in the range of from 1.5 to 5% by weight, thereby enabling the formulation to maintain its viscosity better or longer or under less favourable climatic conditions.
Priority: GB20040010616 Applic. Date: 2004-05-13; WO2005EP04828 Applic. Date: 2005-05-03
Inventor: BATISTA ANDREA P [FR]
Application No.: US20070286876A1 Published: 13/Dec/2007Title: Skin care compositions comprising low concentrations of skin treatment agents
Applicant/Assignee:
Application No.: 11/894165 Filing Date: 20/Aug/2007
Abstract:Skin care compositions may comprise from about 0.001% to about 0.1% by weight of hexamidine and either or both of (i) from about 0.001% to about 10% by weight of zinc oxide, and/or (ii) from about 0.01% to about 10% by weight of niacinamide.
Priority: US2002-152924 Applic. Date: 2002-05-21; US2001-968154 Applic. Date: 2001-10-01
Inventor: WARREN RAPHAEL [US]; BLEVINS JOHN M [US]; KLOFTA THOMAS J [US]; MINOGUCHI RYO [US]; PENNINGTON REGINA L [US]; STAUDIGEL JAMES A [US]; TANNER PAUL R [US]; VATTER MICHAEL L [US]
Application No.: US20070286880A1 Published: 13/Dec/2007Title: Inoculated spongiform scaffold for transplantation and tissue regeneration
Applicant/Assignee:
Application No.: 11/450625 Filing Date: 08/Jun/2006
Abstract:A spongiform scaffold which comprises epithelial stem cells, and free of mesenchymal cells. A spongiform scaffold comprising precursor keratinocytes for use in a method of transplantion of the scaffold to an epithelial cell target site in a recipient, resulting in growth of said epithelial stem cells and the ingrowth of cells from the body of said recipient to restore tissue. A version of the scaffold is formed from collagen, and in particular, Spongostan(TM).
Priority:
Inventor: VASILIEV ANDREY [RU]; FAIZULIN AYVAR [RU]; KISELIOV IVAN [RU]; ROCOVAYA OLGA [RU]; TANKOVICH NIKOLAI [US]; KHARAZI ALEXANDER [US]
Application No.: US20070287010A1 Published: 13/Dec/2007Title: Composite structures with integral intelligent skin
Applicant/Assignee: GENERAL ATOMICS
Application No.: 11/448284 Filing Date: 07/Jun/2006
Abstract:Composite structures having an integral intelligent skin are made of one or more plies of a structural base material and an intelligent or smart film by molding one or more plies and the film into an integral unitary body with the intelligent film outermost. The intelligent or smart film contains or bears a functionally active or interactive component such as antennae, electronic sensors, electric and/or electronic circuitry, and/or spectrally tailored coatings. A method of making the composite structure in a very economical manner is disclosed.
Priority:
Inventor: MCGOVERN THOMAS R [US]; HUBBARD RONALD N [US]
Application No.: US20070287648A1 Published: 13/Dec/2007Title: DILUTION THICKENED PERSONAL CLEANSING COMPOSITION
Applicant/Assignee: CONOPCO, INC., D/B/A UNILEVER CONOPCO, INC
Application No.: 11/423787 Filing Date: 13/Jun/2006
Abstract:A liquid or flowable cleansing composition is described that contains high levels of anionic and nonionic surfactants and that show a substantial increase in viscosity upon dilution with water. The cleansing composition also contains water soluble EO/PO block copolymer(s).
Priority:
Inventor: MOADDEL TEANOOSH [US]; ABBAS SYED HUSAIN [US]; OZKAN-BAL KIMBERLY [US]
Application No.: US20070287688A1 Published: 13/Dec/2007Title: Pharmaceutical Compositions for Topical Application
Applicant/Assignee: MACRO CHEM CORPORATION
Application No.: 10/564199 Filing Date: 09/Jul/2004
Abstract:Compounds of Formula I are useful as skin penetration enhancing agents: (I) wherein: R represents a linear, saturated or unsaturated, substituted or unsubstituted hydrocarbyl radical
and X represents a -(CO)O-, -O(CO)-, C-O, CONH, O, NHCONH, S, or S-O radical. Compositions and methods using these compounds are also described.
Priority: US20030486236P Applic. Date: 2003-07-11; WO2004US21855 Applic. Date: 2004-07-09
Inventor: CHAN THOMAS [US]; KRAUSER SCOTT [US]
Application No.: US20070287689A1 Published: 13/Dec/2007Title: Therapeutic And/Or Preventive Agents For Chronic Skin Diseases
Applicant/Assignee: KYOWA HAKKO KOGYO CO., LTD
Application No.: 11/576972 Filing Date: 13/Oct/2005
Abstract:The present invention provides: a therapeutic and/or preventive agent for chronic skin diseases which comprises (a) a phosphodiesterase (PDE)-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a steroid agent as active ingredients
a therapeutic and/or preventive agent for chronic skin diseases to be administered simultaneously or separately with an interval which comprises (a) a PDE-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a steroid agent, as active ingredients
a kit for treating and/or preventing chronic skin diseases characterized by comprising (a) a first component comprising a PDE-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a second component comprising a steroid agent
and the like.
Priority: JP20040299103 Applic. Date: 2004-10-13; JP20050113264 Applic. Date: 2005-04-11; WO2005JP18855 Applic. Date: 2005-10-13
Inventor: HARADA DAISUKE [JP]; KOBAYASHI KATSUYA [JP]; MANABE HARUHIKO [JP]; OHSHIMA ETSUO [JP]
Application No.: US20070287949A1 Published: 13/Dec/2007Title: Transdermal System for Sustained Delivery of Polypeptides
Applicant/Assignee: TRANSPHARMA MEDICAL LTD
Application No.: 10/580875 Filing Date: 15/Mar/2007
Abstract:A transdermal system for sustained delivery of high molecular weight hydrophilic drugs, especially peptide-, polypeptide- or protein-drugs, and methods of use thereof, are provided. The system includes an apparatus that generates micro-channels in the skin of a subject in combination with a transdermal patch comprising at least one drug reservoir layer comprising a polymeric matrix and a therapeutic or immunogenic peptide, polypeptide, or protein. The system provides sustained delivery of therapeutic or immunogenic agents, thereby achieving sustained therapeutic blood concentrations of these agents.
Priority: IL20030159273 Applic. Date: 2003-12-09; WO2004IL01119 Applic. Date: 2004-12-09
Inventor: LEVIN GALIT [IL]; SACKS HAGIT [IL]
Application No.: US20070287950A1 Published: 13/Dec/2007Title: Device and method for single-needle in vivo electroporation
Applicant/Assignee:
Application No.: 11/704591 Filing Date: 09/Feb/2007
Abstract:Described is a device and method for administration of molecules to tissue in vivo for various medical applications, the device comprising a single hypodermic injection needle and at least two spaced elongate electrodes which provide for the ability, when the needle is inserted into tissue, such as skin or muscle, to pulse tissue with a non-uniform electric field sufficient to cause reversible poration of cells lying along or in close proximity to the track made by the needle upon its insertion into said tissue.
Priority: US20060772255P Applic. Date: 2006-02-11
Inventor: KJEKEN RUNE [US]; MATHIESEN IACOB [US]; TJELLE ELISABETH T [US]; MCHUGH GEORGE [US]
Application No.: US20070287971A1 Published: 13/Dec/2007Title: Absorbent articles with feedback signal upon urination
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/724713 Filing Date: 16/Mar/2007
Abstract:Absorbent articles incorporating sensory element members are disclosed. The absorbent articles may be disposable pant like garments designed to assist urinary toilet training such as of young children. Upon urination by the wearer, the article produces a feedback response which is transmitted to the wearer by the sensory element member. Wetness based, temperature based and other feedback responses are disclosed. The feedback response should be immediate and unmistakable to the wearer and also be temporary and harmless.
Priority: US20060788482P Applic. Date: 2006-03-31
Inventor: ROE DONALD CARROLL [US]; NANDREA JENNIFER JOAN [US]; NISHIKAWA MASAHARU [US]
Application No.: US20070288249A1 Published: 13/Dec/2007Title: Integrated Animal Management System And Method
Applicant/Assignee:
Application No.: 11/578392 Filing Date: 18/Mar/2005
Abstract:The present invention relates to a system for the intensive management of animals, the system comprising: animal identification means for identifying individual animals
at least one device for measuring one or more parameters of individual animals
a processor for processing measurements obtained for the one or more parameters, wherein the processed parameter data is used to determine management strategies for individual animals in real-time
and means for implementing management strategies for the animals.
Priority: AU20040901941 Applic. Date: 2004-04-13; AU20040905559 Applic. Date: 2004-09-24; WO2005AU00393 Applic. Date: 2005-03-18
Inventor: ROWE JAMES B [AU]; ATKIN KEVIN D [AU]; SEMPLE STEPHEN J [AU]; RICHARDS JESSICA S [AU]; MURRAY WILLIAM K [AU]; FISHER ANDREW D [AU]; MIRON DAVID J [AU]; EXLEY JOHN P [AU]; COLDITZ IAN G [AU]; KELLY MATTHEW J [CA]; KNOX MALCOLM [AU]; BESIER BROWN [AU]
Application No.: US20070292355A1 Published: 20/Dec/2007Title: Anti-infection augmentation foamable compositions and kit and uses thereof
Applicant/Assignee: FOAMIX LTD
Application No.: 11/732547 Filing Date: 04/Apr/2007
Abstract:Anti-infective foamable composition and kits include a foamable carrier
a therapeutically safe and effective concentration of an anti-infective agent
an augmenting agent selected from the group consisting of a keratolytic agent and a skin penetration enhancer
and a propellant. The composition is housed in a container and upon release is expandable to form a breakable foam. The foamable carrier is selected to generate a foam of good or excellent quality in the presence of the augmenting agent and anti-infective agent. Methods for treating, alleviating or preventing a disorder of the skin, a body cavity or mucosal surface, wherein the disorder involves a fungal, bacterial or viral infection as one of its etiological factors, is described.
Priority: IL20020152486 Applic. Date: 2002-10-25; US2005-532618 Applic. Date: 2005-12-22; US2004-835505 Applic. Date: 2004-04-28; US2004-922358 Applic. Date: 2004-08-20; US2005-041921 Applic. Date: 2005-01-24; US2004-911367 Applic. Date: 2004-08-04; US2006-448490 Applic. Date: 2006-06-07; WO2003IB05527 Applic. Date: 2003-10-24; US20030492385P Applic. Date: 2003-08-04; US20030530015P Applic. Date: 2003-12-16; US20030497648P Applic. Date: 2003-08-25; US20020429546P Applic. Date: 2002-11-29; US20050688244P Applic. Date: 2005-06-07; US20060789186P Applic. Date: 2006-04-04; US20060861620P Applic. Date: 2006-11-29; US20070880434P Applic. Date: 2007-01-12
Inventor: TAMARKIN DOV [IL]; FRIEDMAN DORON [IL]; EINI MEIR [IL]
Application No.: US20070292359A1 Published: 20/Dec/2007Title: Polypropylene glycol foamable vehicle and pharmaceutical compositions thereof
Applicant/Assignee: FOAMIX LTD
Application No.: 11/811140 Filing Date: 07/Jun/2007
Abstract:The present invention teaches a foamable pharmaceutical carrier comprising polypropylene glycol (PPG) alkyl ether, a surface-active agent water and a liquefied hydrocarbon gas propellant
and pharmaceutical compositions thereof. The present invention further teaches a foamable pharmaceutical carrier comprising polypropylene glycol (PPG) alkyl ether, a surface-active agent, and a liquefied hydrocarbon gas propellant
and pharmaceutical compositions thereof.
Priority: IL20020152486 Applic. Date: 2002-10-25; US2006-481596 Applic. Date: 2006-07-06; US2004-911367 Applic. Date: 2004-08-04; US2005-532618 Applic. Date: 2005-12-22; WO2003IB05527 Applic. Date: 2003-10-24; US2006-488989 Applic. Date: 2006-07-19; US2004-835505 Applic. Date: 2004-04-28; US2004-922358 Applic. Date: 2004-08-20; US2005-124676 Applic. Date: 2005-05-09; US2007-717897 Applic. Date: 2007-03-13; US2005-078902 Applic. Date: 2005-03-11; US20030492385P Applic. Date: 2003-08-04; US20030530015P Applic. Date: 2003-12-16; US20030497648P Applic. Date: 2003-08-25; US20050696878P Applic. Date: 2005-07-06; US20050700702P Applic. Date: 2005-07-19; US20020429546P Applic. Date: 2002-11-29; US20060781868P Applic. Date: 2006-03-13; US20070897638P Applic. Date: 2007-01-26; US20070899176P Applic. Date: 2007-02-02; US20060811627P Applic. Date: 2006-06-07
Inventor: FRIEDMAN DORON [IL]; TAMARKIN DOV [IL]; FEIMAN NAOMI [IL]; SCHUZ DAVID [IL]; BERMAN TAL [IL]
Application No.: US20070292374A1 Published: 20/Dec/2007Title: Personal care products containing high refractive index esters and methods of preparing the same
Applicant/Assignee: INOLEX INVESTMENT COMPANY
Application No.: 11/895759 Filing Date: 27/Aug/2007
Abstract:The invention includes personal care compositions and methods of preparing these personal care compositions that include incorporation of a polyol polyester that is the reaction product of an aliphatic polyol that does not contain an ether group, and benzoic acid, wherein the resultant polyol polyester has a refractive index at 25 DEG C. of greater than about 1.5. The aliphatic polyol may have two to three carbon atoms. Alternatively, the invention includes personal care compositions and methods of preparing personal care compositions including incorporating a polyol polyester into a personal care formulation. The polyol polyester is represented by formula (I): wherein R is an aliphatic alkyl group that does not contain an ether group and has a refractive index of greater than about 1.5 at 25 DEG C. Also described are methods of preparing personal care compositions comprising a first phase and a second phase, wherein the second phase contains any of the polyol polyesters described above.
Priority: US2004-819589 Applic. Date: 2004-04-07
Inventor: BURGO ROCCO [US]
Application No.: US20070292375A1 Published: 20/Dec/2007Title: Piperidinium compounds and cosmetic compositions containing them
Applicant/Assignee: BEIERSDORF AG
Application No.: 11/449720 Filing Date: 09/Jun/2006
Abstract:Cosmetic or dermatological compositions which comprise at least one piperidinium salt, preferably a 4-[(2-cyclopentyl-2-hydroxyphenylacetyl)oxy]-1,1-dimethyl-piperidinium salt, and the use thereof, particularly as antiperspirants. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
Priority:
Inventor: WOEHRMANN MICHAEL [DE]; TERSTEGEN LARA [DE]; MARTIN ANNETTE [DE]; SULZBERGER MELANIE [DE]
Application No.: US20070292420A1 Published: 20/Dec/2007Title: Anti-IL-6 Antibodies, Compositions, Methods and Uses
Applicant/Assignee: CENTOCOR, INC
Application No.: 11/832323 Filing Date: 01/Aug/2007
Abstract:The present invention relates to at least one novel chimeric, humanized or CDR-grafted anti-IL-6 antibodies derived from the murine CLB-8 antibody, including isolated nucleic acids that encode at least one such anti-IL-6 antibody, vectors, host cells, transgenic animals or plants, and methods of making and using thereof, including therapeutic compositions, methods and devices.
Priority: US2002-280716 Applic. Date: 2002-10-26; US20010332743P Applic. Date: 2001-11-14
Inventor: GILES-KOMAR JILL [US]; KNIGHT DAVID [US]; PERITT DAVID [US]; TRIKHA MOHIT [US]
Application No.: US20070292438A1 Published: 20/Dec/2007Title: Novel Gene Disruptions, Compositions and Methods Relating Thereto
Applicant/Assignee:
Application No.: 10/583466 Filing Date: 13/Dec/2004
Abstract:The present invention relates to transgenic animals, as well as compositions and methods relating to the characterization of gene function. Specifically, the present invention provides transgenic mice comprising disruptions in PRO224, PRO9783, PRO1108, PRO34000, PRO240, PRO943, hu A33, PRO230, PRO178, PRO1199, PRO4333, PRO1336, PRO19598, PRO1083, hu TRPM2 or PRO1801 genes. Such in vivo studies and characterizations may provide valuable identification and discovery of therapeutics and/or treatments useful in the prevention, amelioration or correction of diseases or dysfunctions associated with gene disruptions such as neurological disorders
cardiovascular, endothelial or angiogenic disorders
eye abnormalities
immunological disorders
oncological disorders
bone metabolic abnormalities or disorders
lipid metabolic disorders
or developmental abnormalities.
Priority: US20030530043P Applic. Date: 2003-12-16; WO2004US41721 Applic. Date: 2004-12-13
Inventor: ANDERSON STEPHEN J [US]; BRENNAN JANE [GB]; DE SAUVAGE FREDERIC J [US]; DING ZHIYONG [US]; EDWARDS JOEL [US]; FIKES NELDA A [US]; HUANG WENHU [US]; OUYANG WENJUN [US]; RANGEL CAROLINA [US]; SANGHA MAMTA [US]; SHI ZHENG-ZHENG [US]; SPARKS MARY J [US]; TRACKEY JOSEPH [US]; VETTER MELISSA [US]; WANG CHING-YUN [US]; WOODINGS JESSICA [US]
Application No.: US20070292439A1 Published: 20/Dec/2007Title: Antagonist Anti-Cd40 Monoclonal Antibodies and Methods for Their Use
Applicant/Assignee: NOVARTIS VACCINES AND DIAGNOSTICS, INC
Application No.: 11/587911 Filing Date: 27/Jul/2007
Abstract:Compositions and methods for inhibiting CD40-directed activities that are mediated via the binding of C4BP to CD40 are provided. The compositions of the invention include anti-CD40 antibodies, or antigen-binding fragments thereof, that have the following characteristics: 1) are free of significant CD40 agonist activity when bound to CD40 antigen
and 2) are capable of specifically binding to CD40 antigen expressed on the surface of cells, wherein this binding to CD40 antigen blocks C4BP-mediated CD40 signaling, thereby inhibiting one or more CD40-directed activities. These antagonist anti-CD40 antibodies can effectively be used to treat CD40-associated diseases that are mediated by C4BP stimulation of CD40 signaling, including cancers, such as B cell-related cancers and solid tumors, and diseases or disorders that have an autoimmune and/or inflammatory component, including organ and tissue transplant rejection.
Priority: US20040565775P Applic. Date: 2004-04-27; WO2005US14359 Applic. Date: 2005-04-27
Inventor: LUQMAN MOHAMMAD [US]
Application No.: US20070292461A1 Published: 20/Dec/2007Title: Oleaginous pharmaceutical and cosmetic foam
Applicant/Assignee: FOAMIX LTD
Application No.: 11/653205 Filing Date: 12/Jan/2007
Abstract:The invention relates to stable pharmaceutical or cosmetic foam compositions containing certain active agents, having unique therapeutic properties and methods of treatment using such compositions. The foamable composition includes at least one solvent comprising polyethylene glycol (PEG) or PEG derivative and mixtures thereof, or comprising propylene glycol, wherein the solvent is present at a concentration of about 70% to about 96.5% by weight of the total composition, at least a non-ionic surface-active agent at a concentration of about 0.1% to less than about 10% by weight of the total composition.
Priority: US2004-911367 Applic. Date: 2004-08-04; US2006-430599 Applic. Date: 2006-05-09; US2004-835505 Applic. Date: 2004-04-28; US20030492385P Applic. Date: 2003-08-04; US20030530015P Applic. Date: 2003-12-16; US20050679020P Applic. Date: 2005-05-09; US20060784793P Applic. Date: 2006-03-21
Inventor: TAMARKIN DOV [IL]; FRIEDMAN DORON [IL]; EINI MEIR [IL]; BESONOV ALEX [IL]; DANZIGER JORGE [IL]; SCHUZ DAVID [IL]; BERMAN TAL [IL]
Application No.: US20070292463A1 Published: 20/Dec/2007Title: COMPOSITIONS AND METHODS COMPRISING ENERGIZABLE PARTICLES FOR HEALTH USE
Applicant/Assignee:
Application No.: 11/846111 Filing Date: 28/Aug/2007
Abstract:The present invention provides a composition comprising a topical composition base and a plurality of particles selected from the group consisting of magnetic particles, particles comprising microcircuit chips, and combinations thereof. The composition can further comprise one or more active agents. The particles and/or active agent(s) can optionally be encapsulated and/or coated. Methods for making and using the composition are also provided.
Priority: US2005-318191 Applic. Date: 2005-12-22; US20060825920P Applic. Date: 2006-09-17
Inventor: SPECTOR DONALD [US]
Application No.: US20070292527A1 Published: 20/Dec/2007Title: Composition for the cosmetic treatment of age-related dermatological symptoms
Applicant/Assignee: DAIMLERCHRYSLER AG
Application No.: 10/577976 Filing Date: 03/Nov/2004
Abstract:A composition comprising an extract of a deep sea fish
and an extract of rooibos aspalathus linearis)
and optionally an extract of bearberry (arctostaphylos uva-ursi) as active components thereof
and optionally one or more fillers or ancillary agents conventionally used in the formulation of compositions is provided. Upon administration, the composition has beneficial effect in relation to the cosmetic treatment of age-related dermatological symptoms, such as wrinkled and/or aged skin as well as hair loss.
Priority: DK20030001631 Applic. Date: 2003-11-03; WO2004DK00759 Applic. Date: 2004-11-03
Inventor: CHRISTENSEN FLEMMING K [DK]
Application No.: US20070292537A1 Published: 20/Dec/2007Title: Method and composition for reducing appearance of wrinkles
Applicant/Assignee:
Application No.: 11/789017 Filing Date: 23/Apr/2007
Abstract:The present invention provides a cosmetic composition having a cosmetically acceptable vehicle and one or more gap junction inhibitors and/or one or more choline acetyl transferase (CAT) inhibitors in an amount effective for reducing the appearance of deep wrinkles on the skin. Also provided is a method of reducing the appearance of deep wrinkles on the skin, including the steps of topically applying to the skin the above cosmetic composition in an amount and for a period of time sufficient to reduce the appearance of deep wrinkles on the skin.
Priority: WO2005US46190 Applic. Date: 2005-12-20; US20040638147P Applic. Date: 2004-12-22
Inventor: JONES BRIAN C [US]; HINES MICHELLE D [US]
Application No.: US20070292676A1 Published: 20/Dec/2007Title: Microcapsules Loaded with Active Ingredients and a Method for Their Preparation
Applicant/Assignee:
Application No.: 10/566369 Filing Date: 01/Aug/2004
Abstract:The invention relates to microcapsules having a core material encapsulated within a microcapsular shell, the core material comprises at least one active ingredient, wherein the microcapsular shell comprises at least one inorganic polymer comprising polymerized precursors obtained by in-situ polymerization of the precursors
wherein the concentration of the core material based total weight of the microcapsules is above 95% w/w. The invention further relates to a composition and to a suspension comprising the microcapsules. The invention additionally relates to a process for preparing the microcapsules.
Priority: US20030491295P Applic. Date: 2003-07-31; WO2004IL00702 Applic. Date: 2004-08-01
Inventor: NAIGERTSIK OLEG [IL]; ROTHSCHILD SOREL [IL]; ROTTMAN CLAUDIO [IL]
Application No.: US20070293414A1 Published: 20/Dec/2007Title: Detergent compositions for cleaning and fabric care
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/818473 Filing Date: 14/Jun/2007
Abstract:Detergent compositions comprising selected deposition polymers for improved deposition of fabric care benefit agents, such as organosilicones, polyolefin dispersions, polymer latexes, microencapsulated fabric care actives, onto fabrics through the laundering operation.
Priority: US20060815241P Applic. Date: 2006-06-20
Inventor: PANANDIKER RAJAN KESHAV [US]; SIVIK MARK ROBERT [US]; MCCHAIN ROBERT JOE [US]; BUESCHER SUSAN EILEEN [US]; ROTHGEB TIMOTHY MICHAEL [US]; SHEETS CONNIE LYNN [US]; KINDEL PAUL FRANCIS [US]
Application No.: US20070293433A1 Published: 20/Dec/2007Title: Methods of treating aging of skin with oligosaccharides in cosmetic or dermatological compositions that stimulate adhesion of keratinocytes to major proteins of the dermoepidermal junction and restore epidermal cohesion
Applicant/Assignee: LABORATOIRES DE BIOLOGIE VEGETALE YVES ROCHER, A CORPORATION OF FRANCE
Application No.: 11/894945 Filing Date: 22/Aug/2007
Abstract:A method of treating aging of skin including applying a therapeutically effective amount of an anti-aging dermatological care composition including at least one cosmetic formulation agent and oligogalacturonides having a degree of polymerization between 1 and 5 that stimulates adherence of basal keratinocytes to laminin V and/or collagen IV and reduces communication disturbances between a subject's dermis and epidermis and reduces diminishment in interkeratinocyte cohesion within the epidermis, to skin.
Priority: FR20010014463 Applic. Date: 2001-11-08; US2004-839420 Applic. Date: 2004-05-05; WO2002FR03844 Applic. Date: 2002-11-08
Inventor: LUBRANO CHRISTIAN [FR]; FLAVET LAURENCE [FR]; SAINTIGNY GAELLE [FR]; ROBIN JEAN-RENAUD [FR]
Application No.: US20070293795A1 Published: 20/Dec/2007Title: Skin Abrasion Apparatus and Method
Applicant/Assignee:
Application No.: 11/697536 Filing Date: 06/Apr/2007
Abstract:A handheld apparatus including an internal motor and a removable treatment paddle. The removable treatment paddle is designed for connection with the internal motor, and typically has a first surface and a second surface. The first surface typically includes an abrasive material formed into or attached to the surface for skin exfoliation, and the second surface is typically a relatively less abrasive surface than the first surface, for aid in infusing at least one topical active into the skin after treatment with the first surface. The improved device also includes a multi-sided handpiece having a plurality of flat sides for ease of handling, and at least one ventilation hole to prevent overheating of the device during operation. The handpiece can also include a fan for proper ventilation through the ventilation holes. In one embodiment, the handpiece includes an insulating sleeve to protect the user's hand from the heat generated from the device, as well as to provide an improved gripping surface for the handpiece and to decrease the level of noise production from the handpiece.
Priority:
Inventor: CARROLL TIMOTHY [US]
Application No.: US20070297996A1 Published: 27/Dec/2007Title: Multi-phase composition comprising a sunscreen
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/472737 Filing Date: 22/Jun/2006
Abstract:Personal care composition comprising a discrete transparent aqueous phase and a discrete non-aqueous phase, wherein the aqueous phase comprises from about 0.05% to about 5% of a polymeric thickener, and from about 50% to about 99.5% water, both by weight of the aqueous phase
and the non-aqueous phase comprises from about 20% to about 90% of a sunscreen selected from the group consisting of oil-soluble sunscreens, oil-insoluble sunscreens, and combinations thereof
and from about 5% to about 40% of an oil thickener, all by weight of the non-aqueous phase
and wherein the ratio of the weight of the aqueous phase to the weight of the non-aqueous phase is from about 1:1 to about 9:1
and wherein the aqueous phase and the non-aqueous phase are visually distinct and form a stable pattern.
Priority:
Inventor: TANNER PAUL ROBERT [US]
Application No.: US20070297997A1 Published: 27/Dec/2007Title: Personal care composition
Applicant/Assignee: THE PROCTER & GAMBLE COMPANY
Application No.: 11/472739 Filing Date: 22/Jun/2006
Abstract:Stable personal care composition comprising from about 1% to about 20% of a non-emulsifying silicone elastomer
from about 0.5% to about 10% of an emulsifying silicone elastomer
from about 5% to about 30% of an oil-soluble sunscreen
from about 1% to about 20% of a sunscreen solvent
and from about 30% to about 80% of a non-polar emollient.
Priority:
Inventor: TANNER PAUL ROBERT [US]
Application No.: US20070298006A1 Published: 27/Dec/2007Title: Dendritic Polymers With Enhanced Amplification and Interior Functionality
Applicant/Assignee: DENDRITIC NANOTECHNOLOGIES, INC
Application No.: 11/630044 Filing Date: 21/Dec/2005
Abstract:Dendritic polymers with enhanced amplification and interior functionality are disclosed. These dendritic polymers are made by use of fast, reactive ring-opening chemistry (or other fast reactions) combined with the use of branch cell reagents in a controlled way to rapidly and precisely build dendritic structures, generation by generation, with cleaner chemistry, often single products, lower excesses of reagents, lower levels of dilution, higher capacity method, more easily scaled to commercial dimensions, new ranges of materials, and lower cost. The dendritic compositions prepared have novel internal functionality, greater stability (e.g., thermal stability and less or no reverse Michael's reaction), and reach encapsulation surface densities at lower generations. Unexpectedly, these reactions of polyfunctional branch cell reagents with polyfunctional cores do not create cross-linked materials. Such dendritic polymers are useful as demulsifiers for oil/water emulsions, wet strength agents in the manufacture of paper, proton scavengers, polymers, nanoscale monomers, calibration standards for electron microscopy, making size selective membranes, and agents for modifying viscosity in aqueous formulations such as paint. When these dendritic polymers have a carried material associated with their surface and/or interior, then these dendritic polymers have additional properties for carrying materials due to the unique characteristics of the dendritic polymer, such as for drug delivery, transfection, and diagnostics.
Priority: WO2005US47635 Applic. Date: 2005-12-21
Inventor: TOMALIA DONALD A [US]; SWANSON DOUGLAS R [US]; HUANG BAOHUA [US]; PULGAM VEERA R [US]; SVENSON SONKE [US]; REYNA LORI A [US]; ZHURAVEL MICHAEL A [US]; CHAUHAN ABHAY S [US]; DEMATTEI CORDELL R [US]; HEINZELMANN JOSEPH R [US]
Application No.: US20070298135A1 Published: 27/Dec/2007Title: TOPICAL HERBAL FORMULATIONS
Applicant/Assignee: BIOBOTANIC CORP
Application No.: 11/750125 Filing Date: 17/May/2007
Abstract:An herbal formulation is described as an effective treatment of burn injuries and chronic wounds. The herbal formulation comprises an extract of Paris and Sanguisorba prepared by infusing Paris and Sanguisorba in a liquid medium having a boiling point of no more than 160 DEG C.
Priority: US20060801971P Applic. Date: 2006-05-18
Inventor: ZHAO LIZHEN [CN]
Application No.: US20070299018A1 Published: 27/Dec/2007Title: Derivatives of Genkwanin and Sakuranetin, Cosmetic and Therapeutic Use Thereof and Preparation Method of Same
Applicant/Assignee:
Application No.: 10/598752 Filing Date: 11/Mar/2005
Abstract:The invention relates to: (i) the use of osyl derivatives of genkwanin and sakuranetin having formula (I) in (a) cosmetics or dermatology and (b) therapeutics
(ii) the use of novel derivatives having formula (I) as industrial products
and (iii) the production method thereof [Formula (I)], wherein symbol [Formula (II)] represents a single or double bond, R represents H or an osyl residue, particularly with structure S<1 >or s<2 >[Formula (III)], Z represents H, an alkyl group at C1-C4, acyl at C1-C5, monosaccharide or sulphate.
Priority: FR20040002554 Applic. Date: 2004-03-11; WO2005FR00596 Applic. Date: 2005-03-11
Inventor: PROST MICHEL [FR]; RAGOT JACQUELINE [FR]; TUBERY PIERRE [FR]
Application No.: US20070299032A1 Published: 27/Dec/2007Title: Method and Composition for Thickening Hair
Applicant/Assignee: SHISEIDO COMPANY, LTD
Application No.: 10/578507 Filing Date: 10/Nov/2004
Abstract:The present invention provides a method for maintaining and promoting hair thickening by increasing the expression of keratinocyte growth factor (FGF-7) in hair follicle cells, and preferably dermal papilla cells, a composition for increasing expression of FGF-7 that contains adenosine and/or a derivative thereof, and particularly, an external scalp preparation for maintaining and promoting hair thickening.
Priority: JP20030381470 Applic. Date: 2003-11-11; WO2004JP17037 Applic. Date: 2004-11-10
Inventor: EHAMA RITSUKO [JP]; IINO MASATO [JP]; NAKAZAWA YOSUKE [JP]; TAJIMA MASAHIRO [JP]; OGOU MASASHI [JP]; ARASE SEIJI [JP]
Application No.: US20070299046A1 Published: 27/Dec/2007Title: Orally available light-independent antineoplastic compounds
Applicant/Assignee:
Application No.: 11/474890 Filing Date: 26/Jun/2006
Abstract:Pheophorbide derivative compounds which can inhibit cell proliferation and angiogenesis in a light-independent manner are disclosed and claimed. Importantly, these compounds exhibit low toxicity, and are orally/subcutaneous/intravenously/transdermally/topically available, thus having value as new potential agents to treat cancer or diseases related to imbalance in cell proliferation and angiogenesis.
Priority:
Inventor: BROOKS MAI NGUYEN [US]; NORRIS ANDREW JOHN [US]
Application No.: US20070299047A1 Published: 27/Dec/2007Title: Combination of Organic Compounds
Applicant/Assignee:
Application No.: 11/574994 Filing Date: 08/Sep/2005
Abstract:The present invention relates to a pharmaceutical composition, comprising a PPAR agonist, or pharmaceutically acceptable salts thereof, alone or in combination with at least one active ingredient selected from the group consisting of (i) HDL increasing compounds
(ii) anti-diabetics
(iii) an anti-hypertensive agent
(iv) cholesterol absorption modulator
(v) apo-A1 analogs and mimetics
(vi) renin inhibitors
(vii) thrombin inhibitors
(viii) aldosterone inhibitors
(ix) GLP-1 agonists
(x) glucagon receptor antagonists
(xi) cannabinoid receptor 1 antagonists
(xii) anti-obesity agents
and (xiii) inhibitors of platelet aggregation or, in each case, a pharmaceutically acceptable salt thereof
and optionally a pharmaceutically acceptable carrier.
Priority: US20040608310P Applic. Date: 2004-09-09; US20040609577P Applic. Date: 2004-09-14; US20050689738P Applic. Date: 2005-06-10; WO2005US32224 Applic. Date: 2005-09-08
Inventor: MAHER WILLIAM [US]; MERCURI MICHELE [US]; NEVATIA MEENAKSHI [CH]; CHEN HONG [US]; WANG PEI-RAN [US]
Application No.: US20070299050A1 Published: 27/Dec/2007Title: Fused Tricyclic Compounds as Inhibitors of Tumor Necrosis Factor-Alpha
Applicant/Assignee: NICHOLAS PIRAMAL INDIA LIMITED PIRAMAL LIFE SCIENCES LIMITED
Application No.: 11/667580 Filing Date: 08/Nov/2005
Abstract:Compounds of formula 1: are disclosed, wherein V is CH2
W is S(O)m
m is the integer 0, 1 or 2
U is O, C(O), CR13R14 or NR15
where R13 is H, alkyl
R14 is H, OH, OR13 or OCOR13
R15 is H, alkyl, cycloalkyl, alkenyl, C(O)R13, C(O)OR13 or alkylaminocarbonyl
R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein. These compounds are inhibitors of tumor necrosis factor-alpha (TNF-alpha) and are useful as medicaments for the treatment and prevention of disorders caused by increased TNF-alpha activity, in particular inflammations.
Priority: IN2004MU01226 Applic. Date: 2004-11-10; US20040637217P Applic. Date: 2004-12-17; WO2005IB53654 Applic. Date: 2005-11-08
Inventor: LAL BANSI [IN]; SHARMA SOMESH [IN]; GHOSH USHA [IN]; BAL-TEMBE SWATI [IN]; MORE TULSIDAS [IN]; GAGARE PRAVIN [IN]; JADHAV SUNIL [IN]; PATIL SHASHIKANT [IN]; KULKARNI-ALMEIDA ASHA [IN]; PARIKH SAPNA [IN]; PANICKER RADHA [IN]; DAMRE ANAGHA [IN]; GUPTE RAVINDRA [IN]
Application No.: US20070299090A1 Published: 27/Dec/2007Title: SUBSTITUTED 8-AMINOALKOXY-XANTHINE COMPOUNDS AND COMPOSITIONS USEFUL IN THE TREATMENT OF HYPERLIPIDEMIA AND DIABETES
Applicant/Assignee: SANOFI-AVENTIS DEUTSCHLAND GMBH
Application No.: 11/674261 Filing Date: 13/Feb/2007
Abstract:Compounds for the treatment of elevated blood glucose levels and the physiological and metabolic disorders arising therefrom are disclosed which are inhibitors of the enzyme dipeptidyl peptidase IV (DDP-IV) and comprise novel substituted bicyclic 8-pyrrolidinoxanthines of formula I and their derivatives: wherein the various R-groups are defined herein. These compounds may be combined with other secondary active compounds which also are effective in the treatment of said disorders and the disease states or physiological manifestations arising therefrom.
Priority: DE200410039507 Applic. Date: 2004-08-14; WO2005EP08283 Applic. Date: 2005-07-30
Inventor: SCHOENAFINGER KARL [DE]; JAEHNE GERHARD [DE]; DEFOSSA ELISABETH [DE]; BUNING CHRISTIAN [DE]; TSCHANK GEORG [DE]; WERNER ULRICH [DE]
Application No.: US20070299113A1 Published: 27/Dec/2007Title: Metabotropic glutamate receptor modulators
Applicant/Assignee: MERZ PHARMA GMBH & CO. KGAA
Application No.: 11/821492 Filing Date: 22/Jun/2007
Abstract:The invention relates to imidazothiazole derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are group I mGluR modulators and are therefore useful for the control and prevention of various disorders, including acute and/or chronic neurological disorders.
Priority: US20060816171P Applic. Date: 2006-06-23
Inventor: KALVINSH IVARS [LV]; KAULINA LARISA [LV]; KAUSS VALERJANS [LV]; ZEMRIBO RONALDS [LV]; DANYSZ WOJCIECH [DE]; HENRICH MARKUS [DE]; PARSONS CHRISTOPHER GRAHAM RAP [DE]; WEIL TANJA [DE]; ERDMANE ELINA [LV]