, n and B have meanings given in the description which are useful as competitive inhibitors of trypsin-like proteases, such as thrombin, and in particular in the treatment of conditions where inhibition of thrombin is required (e.g. thrombosis) or as anticoagulants.Priority: SE19980004313 Applic. Date: 1998-12-14; WO1999SE02316 Applic. Date: 1999-12-10; US2004-815954 Applic. Date: 2004-04-02; US2000-509032 Applic. Date: 2000-03-21
Inventor: INGHARDT TORD [SE]; KARLSSON OLLE [SE]; LINSCHOTEN MARCEL [SE]; NYSTROM JAN-ERIK [SE]
Application No.: US20070250106A1 Published: 25/Oct/2007Title: SELF-FLUSHING MEDICAL APPARATUS
Applicant/Assignee: BOSTON SCIENTIFIC SCIMED, INC
Application No.: 11/379884 Filing Date: 24/Apr/2006
Abstract:An apparatus for use in a therapeutic medical procedure that may include an elongate sheath having a longitudinal axis, an outer surface a distal end and a proximal end, the elongate sheath having a first lumen having a first cross-sectional area running from an first opening at the distal end to a first point proximal the distal end and a second lumen fluidly connected to the first lumen, the second lumen having a distal end at or proximal the first point and a second cross-sectional area less than the first cross-sectional area, the second lumen having a portion running generally along the elongate axis
and an elongate member having a first portion having a third cross-sectional area, a proximal end and a distal end and having a therapeutic device disposed on the elongate member proximate the distal end, the therapeutic device having a first configuration having a fourth cross-sectional area, wherein the elongate member is disposed in the first and second lumens and the distal protection device is disposed in the first lumen, wherein when the distal protection device is disposed in the first lumen, the elongate sheath has a second opening proximate and proximal the distal protection device and a third opening proximal the second opening in which the elongate member is partially disposed, and wherein the second opening is in fluid communication with the third opening when the distal protection device is disposed in the first lumen.
Priority:
Inventor: KIM ELIOT T [US]
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.: US20070258894A1 Published: 08/Nov/2007Title: System and Method for Real-Time Diagnosis, Treatment, and Therapeutic Drug Monitoring
Applicant/Assignee:
Application No.: 10/588749 Filing Date: 28/Feb/2005
Abstract:Systems and methods for diagnosing and/or treating diseases as well as monitoring disease treatment. For diagnosis, the present invention uses nanoparticle-based assemblies, which comprise a nanoparticle
a surrogate marker
and a means for detecting a specific chemical entity. In certain embodiments, nanoparticle-based assemblies include a payload for simultaneous diagnosis and treatment of disease. In further embodiments, a therapeutic drug and therapeutic drug marker are administered to a patient to monitor disease treatment. Bodily fluid samples are analyzed using sensor technology to detect the presence of surrogate and/or therapeutic drug markers to provide an efficient and accurate means for diagnosing a disease and/or monitoring disease treatment.
Priority: US2000-708789 Applic. Date: 2000-11-08; WO2005US06355 Applic. Date: 2005-02-28
Inventor: MELKER RICHARD J [US]; SACKELLARES JAMES C [US]; GOLD MARK S [US]; DENNIS DONN M [US]
Application No.: US20070259809A1 Published: 08/Nov/2007Title: Methods of Using High Affinity Atiii Variants
Applicant/Assignee:
Application No.: 10/584640 Filing Date: 10/Jan/2005
Abstract:Disclosed are compositions and methods related to binding of ATIII under low and high shear rate conditions.
Priority: US20040535360P Applic. Date: 2004-01-09; US20040618746P Applic. Date: 2004-10-14; WO2005US00843 Applic. Date: 2005-01-10
Inventor: BOCK SUSAN C [US]
Application No.: US20070264194A1 Published: 15/Nov/2007Title: Peptides That Bind To Atherosclerotic Lesions
Applicant/Assignee: THE SCRIPPS RESEARCH INSTITUTE
Application No.: 10/486318 Filing Date: 09/Aug/2002
Abstract:The present invention provides peptides that selectively bind to mammalian atherosclerotic lesions. The present invention also provides methods for in vivo identification of peptides capable of binding to biomolecules as well as methods for identifying the targets of such binding moieties. Methods to diagnose or treat pathologic conditions that involve atherosclerotic lesions are also provided by the invention that involve administering to a mammal a peptide attached to a reporter molecule or a therapeutic agent, respectively.
Priority: US20010311507P Applic. Date: 2001-08-10; WO2002EP08942 Applic. Date: 2002-08-09
Inventor: LIU CHENG [US]; EDGINGTON THOMAS S [US]; PRESCOTT MARGARET F [US]
Application No.: US20070265615A1 Published: 15/Nov/2007Title: Electrosurgical instrument with suction, irrigation and means to collect blood
Applicant/Assignee:
Application No.: 11/473103 Filing Date: 23/Jun/2006
Abstract:An electrosurgical instrument with electrode, suction, optional irrigation and means to bend the distal part of the surrounding suction tube is described. A distal part of the suction tube (around the electrode) has two members, whereas one member can be engaged inside the other-to various degrees-in order to control the length of the suction tube and its relation to the tip of the electrode. Means to fixate the electrode within the suction tube are described. Also described are means to evacuate smoke, blood, irrigation anticoagulant fluid and debris via a suction tube to a separation chamber and evacuation of the gaseous portions by a vacuum machine. The separation chamber serves as a blood collection container (the blood could then be re-infused to the patient!). Irrigation means of isotonic fluid with blood-anticoagulant combined with the suction are described. Combination of the various functions and options could be utilized for building various useful surgical instruments.
Priority: IL20060175493 Applic. Date: 2006-05-09
Inventor: BEN-SIMHON HAIM [IL]
Application No.: US20070270939A1 Published: 22/Nov/2007Title: Drug Delivery Device
Applicant/Assignee: TAYSIDE FLOW TECHNOLOGIES LTD
Application No.: 10/597677 Filing Date: 04/Feb/2005
Abstract:A drug delivery device ( 1 ) is disclosed. The device comprises a vascular implant having a helical formation ( 4 ) that is capable of inducing helical flow of blood passing it. A drug is releasably associated with the helical formation.
Priority: GB20040002736 Applic. Date: 2004-02-06; WO2005GB00379 Applic. Date: 2005-02-04
Inventor: HOOD ROBERT G [GB]; DUFF CRAIG M [GB]
Application No.: US20070275889A1 Published: 29/Nov/2007Title: Gene Expression Technique
Applicant/Assignee: DELTA BIOTECHNOLOGY LIMITED
Application No.: 10/584424 Filing Date: 23/Dec/2004
Abstract:The present invention provides a method for producing heterologous protein comprising: (a) providing a host cell comprising a 2 mum-family plasmid, the plasmid comprising a gene encoding a protein comprising the sequence of a chaperone protein and a gene encoding a heterologous protein
(b) culturing the host cell in a culture medium under conditions that allow the expression of the gene encoding the chaperone protein and the gene encoding a heterologous protein
(c) purifying the thus expressed heterologous protein from the cultured host cell or the culture medium.
Priority: GB20030029681 Applic. Date: 2003-12-23; WO2004GB05462 Applic. Date: 2004-12-23
Inventor: SLEEP DARRELL [GB]; SHUTTLEWORTH GILLIAN [GB]; FINNIS CHRISTOPHER JOHN A [GB]
Application No.: US20070282280A1 Published: 06/Dec/2007Title: Intravascular Line and Port Cleaning Methods, Methods of Administering an Agent Intravascularly, Methods of Obtaining/Testing Blood, and Devices for Performing Such Methods
Applicant/Assignee: HYPROTEK, INC
Application No.: 11/745843 Filing Date: 08/May/2007
Abstract:An intravascular port access device includes a first component having a chamber configured to attach reversibly to an intravenous line port. A second component reversibly attaches to the first component and contains a disinfecting agent and an applicator material. The second component is configured to be reversibly received over external surfaces of the intravenous line port. A method of cleansing an intravenous line port includes providing a port cleaning device having a first component with a chamber containing a first cleaning agent. A second component includes a second cleaning agent. A third component has a microbiocidal agent and is reversibly attached to the first component. The second component is removed from the device, the external surfaces of the port are contacted with the second cleaning agent, the first cleaning agent is ejected from the chamber into the port, and the third component is used to cap the port.
Priority: US20060842194P Applic. Date: 2006-08-31; US20060747606P Applic. Date: 2006-05-18; US20070895621P Applic. Date: 2007-03-19
Inventor: TENNICAN PATRICK O [US]
Application No.: US20070284298A1 Published: 13/Dec/2007Title: PLASMA EXTRACTION APPARATUS
Applicant/Assignee: CHROMEDX INC
Application No.: 11/835631 Filing Date: 08/Aug/2007
Abstract:Some analyzers cannot measure blood analytes from a sample of whole blood, but can measure the analytes in plasma extracted from the whole blood. Some embodiments of the invention provide a disposable apparatus that is suitable for extracting plasma from whole blood received from a blood supply. The blood supply includes one of a tube containing blood, a syringe containing blood, a drop of blood on the skin resulting from a pin prick, a vein, an artery, and an arterial line. The apparatus includes a housing, and arranged within the housing is a porous membrane, a filtration chamber, and a plasma collection chamber. The porous membrane forms a barrier between the whole blood and the plasma extracted from the whole blood. The filtration chamber receives the whole blood for plasma extraction, and the plasma collection chamber collects the plasma extracted from the whole blood.
The apparatus also includes a blood flow path within the housing, and the blood flow path includes the filtration chamber. Means for enabling blood flow in the blood flow path are provided, and means for enabling plasma extraction and plasma removal from the housing are also provided.
Priority: CA20052507323 Applic. Date: 2005-05-13; US2006-432616 Applic. Date: 2006-05-12
Inventor: SAMSOONDAR JAMES [CA]
Application No.: US20070292490A1 Published: 20/Dec/2007Title: Production of tissue factor in plants
Applicant/Assignee:
Application No.: 11/165590 Filing Date: 22/Jun/2005
Abstract:The instant invention provides transgenic plants that express mammalian, e.g., human, recombinant tissue factor (rhTF) as well as methods for making rhTF. The invention further provides rhTF or functional fragment thereof that are obtained from a transgenic plant. The invention also provides methods of treating a subject using the rhTF or a fragment thereof.
Priority: US20040583187P Applic. Date: 2004-06-25
Inventor: NEGROUK VALENTIN [US]; WONG HING C [US]; TAYLOR DEAN [US]; HAN KAI-PING [US]
Application No.: US20070298021A1 Published: 27/Dec/2007Title: Methods and Compositions for the Treatment or Prevention of Secondary Ischemic Injury
Applicant/Assignee: INDEX PHARMACEUTICALS AB
Application No.: 10/589842 Filing Date: 21/Feb/2005
Abstract:After a primary ischemic injury, which predominantly results in necrosis, there is a secondary injury in the neighbouring tissue, due at least to some extent to apoptosis. This secondary damage is usually not evident until several days after the initial ischemic event. The present invention provides methods of preventing, treating and/or alleviating secondary ischemic damage in a mammalian organ or tissue, comprising a step of administering an effective amount of an NF-kappaB inhibitor to said organ or tissue. Compositions for this purpose are also disclosed.
Priority: SE20040000399 Applic. Date: 2004-02-20; US20040546723P Applic. Date: 2004-02-20; WO2005SE00231 Applic. Date: 2005-02-21
Inventor: VON STEIN OLIVER [SE]; PETTERSSON SVEN [SE]; LIM SAI K [SG]
Application No.: US20080000484A1 Published: 03/Jan/2008Title: Apparatus for vascular and nerve tissue histogenesis and enhancement
Applicant/Assignee:
Application No.: 11/477175 Filing Date: 28/Jun/2006
Abstract:An apparatus for delivering decompressive energy to soft tissues to stimulate cellular expansion through deep penetration of said applied decompressive energy to said soft tissues to stimulate a predetermined reaction to application of said decompressive energy comprising a vessel having an open end and adapted to encompass the soft tissue to be stimulated. A source of decompressive energy in communication with said vessel and a flexible mass affixed to said open end of said vessel to absorb the pressure exerted by delivery of said decompressive energy to said soft tissue, thereby acting as a seal and force diffuser between said vessel and the soft tissue adjacent the periphery of said vessel.
Priority:
Inventor: KAISER DANIEL E [US]
Application No.: US20080000801A1 Published: 03/Jan/2008Title: Automated system, method, and kit for immediate treatment of acute medical condition
Applicant/Assignee:
Application No.: 11/300104 Filing Date: 13/Dec/2005
Abstract:A system, method, and kit for immediate and initial treatment of an acute medical condition. The system, method, and kit may be self-administered in the event of an acute medical condition.
Priority: US20040635800P Applic. Date: 2004-12-13
Inventor: MACKIE ROBERT W JR [US]
Application No.: US20080003214A1 Published: 03/Jan/2008Title: Medicaments Comprising Carbonyl Compounds, And The Use Thereof
Applicant/Assignee:
Application No.: 11/575711 Filing Date: 24/Aug/2005
Abstract:Use of compounds of the formula (I) in which D, E, G, W, X, Y, T, R<1 >and R<2 >have the meaning indicated in Patent Claim 1 , for the prophylaxis and/or therapy of thromboembolic diseases
Priority: DE200410045796 Applic. Date: 2004-09-22; WO2005EP09124 Applic. Date: 2005-08-24
Inventor: CEZANNE BERTRAM [DE]; DORSCH DIETER [DE]; MEDERSKI WERNER [DE]; TSAKLAKIDIS CHRISTOS [DE]; GLEITZ JOHANNES [DE]
Application No.: US20080003231A1 Published: 03/Jan/2008Title: Method of medically treating an individual
Applicant/Assignee:
Application No.: 11/478070 Filing Date: 29/Jun/2006
Abstract:A method immunizing an individual that minimizes the amount of antigen or attenuated organism needed and the number of doses and clinic visits required, while making possible polyvalent simultaneous immunizations. The method comprises the steps of obtaining a sample of blood. Exposing at least a portion of this sample to at least one immunogenic antigen, attenuant or other immunogen. Incubating the exposed sample under specified optimal conditions and introducing this exposed sample into the individual to effect immunization thereof. The method of the invention also provides a method of delivery of materials, other than antigens, throughout an individual's body such as therapeutic drugs, virus vectors, genes, DNA, RNA, isotopes, and other therapeutic substances. A method for the delivery of treatment material to an individual is also provided by this method.
Priority:
Inventor: NALIN DAVID R [US]
Application No.: US20080003564A1 Published: 03/Jan/2008Title: SAMPLE PROCESSING
Applicant/Assignee: IQUUM, INC
Application No.: 11/674117 Filing Date: 12/Feb/2007
Abstract:A sample processing tubule may include at least three segments. Each segment may be defined by the tubule, may be fluidly isolated, at least in part by a breakable seal, may be so expandable as to receive a volume of fluid expelled from another segment, and may be so compressible as to contain substantially no fluid when so compressed. At least one segment may contain at least a control reagent. At least one segment may contain at least one of a nucleic acid amplification reagent and a detection reagent.
Priority: US20060743292P Applic. Date: 2006-02-14
Inventor: CHEN SHUQI [US]; CHEN LINGJUN [US]
Application No.: US20080008693A1 Published: 10/Jan/2008Title: PLASMA-DEPLETED, NON-RED BLOOD CELL-DEPLETED CORD BLOOD COMPOSITIONS AND METHODS OF USE
Applicant/Assignee: STEMCYTE, INC
Application No.: 11/771942 Filing Date: 29/Jun/2007
Abstract:The umbilical cord blood (UCB) compositions of the present invention possess the unique features of having plasma that is substantially depleted from the UCB unit and red blood cells (RBC) that are not depleted from the UCB unit. Such UCB units can be prepared by a process that combines plasma depletion with cryopreservation, selection, thawing, and/or transplantation of hematopoietic stem cells to provide superior clinical outcome by maximizing post-processing cell recovery and post-thaw infusion cell dose. Methods for treating a wide variety of malignant diseases and benign diseases associated with the hematopoietic system by administering the UCB compositions of the present invention are also provided.
Priority: US2006-422017 Applic. Date: 2006-06-02; US20050733956P Applic. Date: 2005-11-03; US20050687127P Applic. Date: 2005-06-02
Inventor: CHOW ROBERT [US]
Application No.: US20080008744A1 Published: 10/Jan/2008Title: Novel tissue support
Applicant/Assignee:
Application No.: 11/825478 Filing Date: 06/Jul/2007
Abstract:The present disclosure provides tissue supports which may be utilized by themselves or in combination with other tissue closure means to enhance wound closure and healing. The tissue supports are made of a material which shrinks upon application of heat or light to further support the tissue and/or wound to which it is applied.
Priority: US20060819152P Applic. Date: 2006-07-07
Inventor: PROMMERSBERGER MEGAN [US]
Application No.: US20080009009A1 Published: 10/Jan/2008Title: Device and method for high-throughput quantification of mRNA from whole blood
Applicant/Assignee:
Application No.: 11/803663 Filing Date: 15/May/2007
Abstract:Disclosed are a method, device kit, and automated system for simple, reproducible, and high-throughput quantification of mRNA from whole blood. More particularly, the method, device, kit and automated system involve combinations of leukocyte filters attached to oligo(dT)-immobilized multi-well plates.
Priority: US2004-796298 Applic. Date: 2004-03-09; US2003-698967 Applic. Date: 2003-10-30; WO2003US12895 Applic. Date: 2003-04-24; US20020375472P Applic. Date: 2002-04-24
Inventor: MITSUHASHI MASATO [US]
Application No.: US20080009935A1 Published: 10/Jan/2008Title: STENT DESIGN WITH SHEATH ATTACHMENT MEMBERS
Applicant/Assignee: BOSTON SCIENTIFIC SCIMED, INC
Application No.: 11/857531 Filing Date: 19/Sep/2007
Abstract:A stent is provided having attachment members for allowing attachment of a sheath or sheaths. Accordingly, a practitioner is able to selectively choose a desirable sheath, such as a polymeric sleeve, a biomaterial, or a natural blood vessel, at a point-of-use and attach it to the sheath. The attachment members may be bendable tabs and/or secondary support stents.
Priority: US2001-974653 Applic. Date: 2001-10-10
Inventor: BICEK ANDREW D [US]; GIRTON TIMOTHY S [US]
Application No.: US20080014148A1 Published: 17/Jan/2008Title: Perturbed membrane-binding compounds and methods of using the same
Applicant/Assignee: APOSENSE LTD
Application No.: 11/882490 Filing Date: 02/Aug/2007
Abstract:The present invention relates to compounds that selectively bind to cells undergoing perturbations and alterations of their normal plasma membrane organization, such as cells undergoing apoptosis or activated platelets. The invention further provides methods for utilizing said compounds in medical practice, for diagnostic and therapeutic purposes.
Priority: US2004-799586 Applic. Date: 2004-03-15; US20040536493P Applic. Date: 2004-01-15; US20040537289P Applic. Date: 2004-01-20
Inventor: ZIV ILAN [IL]; SHIRVAN ANAT [IL]
Application No.: US20080015487A1 Published: 17/Jan/2008Title: System and Method for Delivery of Regional Citrate Anticoagulation to Extracorporeal Blood Circuits
Applicant/Assignee: HENRY FORD HEALTH SYSTEM
Application No.: 11/829261 Filing Date: 27/Jul/2007
Abstract:The present invention includes a comprehensive replacement fluid system and method for the delivery of regional citrate anticoagulation (RCA) to extracorporeal blood circuits, wherein the system may include an online clearance monitor (OCM) and a circuit effluent online sensor system (OSS) for the continuous determination of patient plasma content of ultrafilterable solutes.
Priority: WO2007US62589 Applic. Date: 2007-02-22; US20060775729P Applic. Date: 2006-02-22; US20060775728P Applic. Date: 2006-02-22; US20060790882P Applic. Date: 2006-04-11; US20060791055P Applic. Date: 2006-04-11; US20060845646P Applic. Date: 2006-09-19
Inventor: SZAMOSFALVI BALAZS [US]; FRINAK STANLEY [US]; YEE JERRY [US]
Application No.: US20080015598A1 Published: 17/Jan/2008Title: Novel skin staples
Applicant/Assignee:
Application No.: 11/827278 Filing Date: 11/Jul/2007
Abstract:The present disclosure provides composite staples which include legs made of a bioabsorbable shape memory material capable of gripping tissue upon application in vivo and holding the staple in place.
Priority: US20060819965P Applic. Date: 2006-07-11
Inventor: PROMMERSBERGER MEGAN [US]
Application No.: US20080017577A1 Published: 24/Jan/2008Title: Membrane-based Double-layer Tube for Sample Collections
Applicant/Assignee: BECTON, DICKINSON AND COMPANY
Application No.: 11/459076 Filing Date: 21/Jul/2006
Abstract:The fluid sample collection device is adapted to collect and separate a fluid sample into constituent parts such as separating plasma or serum from a blood sample. The device includes an evacuated outer container and an inner container. The outer container has a first open end and a second closed end. A pierceable closure closes the first open end thereby defining a first interior chamber. The inner container is contained within the outer container and separates the first interior chamber into an upper chamber portion and lower chamber portion in fluid communication. The inner container defines a second interior chamber separated from the lower chamber portion through a porous membrane. A port is provided for placing the second interior chamber in fluid communication with the first interior chamber. Another aspect of the device relates to a method of using the device to separate plasma or serum from a blood sample.
Priority:
Inventor: YI JIZU [US]; LIN FU CHUNG [US]; MANOUSSAKIS DIMITRIOS [US]; GELFAND CRAIG [US]
Application No.: US20080019985A1 Published: 24/Jan/2008Title: NOVEL TISSUE FACTOR TARGETED THROMBOMODULIN FUSION PROTEINS AS ANTICOAGULANTS
Applicant/Assignee: BAYER SCHERING AG BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Application No.: 11/766155 Filing Date: 21/Jun/2007
Abstract:This invention relates to novel fusion proteins which are comprised of a targeting protein that binds tissue factor (TF), which is operably linked to the thrombomodulin (TM) EGF456 domain alone or in combination with at least one other TM domain selected from the group consisting of the N-terminal hydrophobic region domain, the EGF123 domain, the interdomain loop between EGF3 and EGF4, and the O-glycosylated Ser/Thr-rich domain, or analogs, fragments, derivatives or variants thereof. The fusion protein binds at the site of injury and prevents the initiation of thrombosis. The fusion protein can be used to treat a variety of thrombotic conditions including but not limited to deep vein thrombosis, disseminated intravascular coagulation, and acute coronary syndrome.
Priority: US2003-427805 Applic. Date: 2003-04-30; US20020376566P Applic. Date: 2002-05-01
Inventor: LIGHT DAVID [US]; MCLEAN KIRK [US]
Application No.: US20080020965A1 Published: 24/Jan/2008Title: NOVEL TISSUE FACTOR TARGETED THROMBOMODULIN FUSION PROTEINS AS ANTICOAGULANTS
Applicant/Assignee: BAYER SCHERING AG BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Application No.: 11/766160 Filing Date: 21/Jun/2007
Abstract:This invention relates to novel fusion proteins which are comprised of a targeting protein that binds tissue factor (TF), which is operably linked to the thrombomodulin (TM) EGF456 domain alone or in combination with at least one other TM domain selected from the group consisting of the N-terminal hydrophobic region domain, the EGF123 domain, the interdomain loop between EGF3 and EGF4, and the O-glycosylated Ser/Thr-rich domain, or analogs, fragments, derivatives or variants thereof. The fusion protein binds at the site of injury and prevents the initiation of thrombosis. The fusion protein can be used to treat a variety of thrombotic conditions including but not limited to deep vein thrombosis, disseminated intravascular coagulation, and acute coronary syndrome.
Priority: US2003-427805 Applic. Date: 2003-04-30; US20020376566P Applic. Date: 2002-05-01
Inventor: LIGHT DAVID [US]; MCLEAN KIRK [US]
Application No.: US20080021065A1 Published: 24/Jan/2008Title: NOVEL BENZAMIDINE COMPOUND
Applicant/Assignee: AJINOMOTO CO. INC AJINOMOTO CO., INC
Application No.: 11/832895 Filing Date: 02/Aug/2007
Abstract:Compounds represented by formula (1) and pharmaceutically acceptable salt thereofs: wherein each symbol is as defined in the specification, are useful as inhibitors of an activated blood coagulation factor X. Compositions which contain, as an active ingredient, an FXa selective low-molecular weight FXa inhibitor having a short serum half-life are particularly useful as anticoagulants for an extracorporeal blood circuit.
Priority: JP20050026949 Applic. Date: 2005-02-02; WO2006JP302202 Applic. Date: 2006-02-02
Inventor: TAKAYANAGI MASARU [JP]; TAKEHANA SHUNJI [JP]; OTANI KAYO [JP]; SAITOU YUKI [JP]
Application No.: US20080021366A1 Published: 24/Jan/2008Title: WEARABLE ULTRAFILTRATION DEVICE
Applicant/Assignee: NATIONAL QUALITY CARE, INC FRESENIUS MEDICAL CARE HOLDINGS, INC
Application No.: 11/830695 Filing Date: 30/Jul/2007
Abstract:An ultrafiltration device adapted to be worn on a portion of the body of a patient includes a blood inlet tube leading from a first blood vessel, a blood pump, an anticoagulant reservoir for infusing anticoagulants into the blood, a blood filter including a substrate through which the blood is circulated and filtered, a fluid bag for storing the excess fluid and a blood outlet tube leading to a second blood vessel.
Priority: US2002-251937 Applic. Date: 2002-09-19; US2001-085349 Applic. Date: 2001-11-16
Inventor: GURA VICTOR [US]; RAMBOD EDMOND [US]
Application No.: US20080023399A1 Published: 31/Jan/2008Title: Apparatus and method for continuous particle separation
Applicant/Assignee: THE TRUSTEES OF PRINCETON UNIVERSITY
Application No.: 11/809559 Filing Date: 31/May/2007
Abstract:The invention is directed to an apparatus and a method of separating particles, such as cells, from a heterogeneous fluid, such as blood, where the particles have a large range of sizes.
Priority: US20060809933P Applic. Date: 2006-06-01
Inventor: INGLIS DAVID W [AU]; DAVIS JOHN [US]; AUSTIN ROBERT [US]; STURM JAMES [US]
Application No.: US20080025872A1 Published: 31/Jan/2008Title: Disposable Fluid Sample Collection Device
Applicant/Assignee:
Application No.: 10/578453 Filing Date: 05/Nov/2004
Abstract:A fluid sampling device ( 100 ) that operates by a combination of capillary action to collect a small fluid sample, and by pressure differential when inserted into an analyzer ( 200 ) to expose the fluid sample for testing by the analyzer ( 200 ). The device is especially suited for use as a disposable blood sampling unit designed to interface with a blood analyzer, albeit the concept of the invention may be employed for sampling and testing virtually any fluids.
Priority: US20030517573P Applic. Date: 2003-11-05; WO2004US36909 Applic. Date: 2004-11-05
Inventor: DYKES CHRIS [US]; LANE BEN [US]
Application No.: US20080026474A1 Published: 31/Jan/2008Title: ASSAY FOR DIFFERENTIATING COMPOUNDS THAT MODULATE THE EXTRINSIC AND/OR INTRINSIC COAGULATION PATHWAYS
Applicant/Assignee: BRISTOL-MYERS SQUIBB COMPANY
Application No.: 11/782660 Filing Date: 25/Jul/2007
Abstract:Methods for differentiating compounds that modulate the extrinsic and/or intrinsic coagulation pathways are provided. Also provided are methods for identifying a compound that modulates the extrinsic coagulation pathway. In addition, methods for determining an effective dosage of an anticoagulant in a patient are provided.
Priority: US20060833674P Applic. Date: 2006-07-27
Inventor: WANG XINKANG [US]; HSU MEI-YIN [US]; WONG PANCRAS C [US]
Application No.: US20080031874A1 Published: 07/Feb/2008Title: Treatment of endotoxemia using endotoxin neutralizing agents
Applicant/Assignee:
Application No.: 11/703538 Filing Date: 06/Feb/2007
Abstract:Methods and compositions for selecting a patient suffering from endotoxemia for treatment with an endotoxin neutralizing agent are disclosed comprising: (a) determining the level of endotoxin in the patient's blood
and (b) comparing the endotoxin level in the patient's blood to a predetermined threshold endotoxin level to determine if the patient has elevated endotoxin levels. The methods can further comprise treating patients identified as having elevated levels of endotoxin with an endotoxin neutralizing therapy. The methods provide increased safety and a reduction in risk for critically ill patients.
Priority: US20060765996P Applic. Date: 2006-02-06
Inventor: SANDERS MARTIN E [US]
Application No.: US20080031934A1 Published: 07/Feb/2008Title: Processes for the production of solid dressings for treating wounded tissue
Applicant/Assignee:
Application No.: 11/882872 Filing Date: 06/Aug/2007
Abstract:Disclosed are processes for preparing solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of a fibrinogen component and a fibrinogen activator. Also disclosed are methods for treating wounded tissue using these dressings and frozen and liquid compositions useful for preparing the haemostatic layer(s) of these dressings or for treating wounded tissue in a mammal.
Priority: US20060835423P Applic. Date: 2006-08-04
Inventor: MACPHEE MARTIN [US]; BEALL DAWSON [US]
Application No.: US20080033331A1 Published: 07/Feb/2008Title: Solid dressing for treating wounded tissue
Applicant/Assignee:
Application No.: 11/882874 Filing Date: 06/Aug/2007
Abstract:Disclosed are solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of a fibrinogen component and a fibrinogen activator, wherein the haemostatic layer(s) is cast or formed from a single aqueous solution containing the fibrinogen component and the fibrinogen activator. Also disclosed are methods for treating wounded tissue using these dressings and frozen compositions useful for preparing the haemostatic layer(s) of these dressings.
Priority: US20060835423P Applic. Date: 2006-08-04
Inventor: MACPHEE MARTIN [US]; BEALL DAWSON [US]
Application No.: US20080033332A1 Published: 07/Feb/2008Title: Solid dressing for treating wounded tissue
Applicant/Assignee:
Application No.: 11/882876 Filing Date: 06/Aug/2007
Abstract:Disclosed are solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of fibrinogen and a fibrinogen activator, wherein the fibrinogen is present in an amount between 3.0 mg/cm<2 >of the wound facing surface of the dressing and 13.0 mg/cm<2 >of the wound facing surface of the dressing. Also disclosed are methods for treating wounded tissue.
Priority: US20060835423P Applic. Date: 2006-08-04
Inventor: MACPHEE MARTIN [US]; BEALL DAWSON [US]
Application No.: US20080033333A1 Published: 07/Feb/2008Title: Solid dressing for treating wounded tissue
Applicant/Assignee:
Application No.: 11/882879 Filing Date: 06/Aug/2007
Abstract:Disclosed are solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of a fibrinogen component and thrombin, wherein the thrombin is present in an amount between 0.250 Units/mg of fibrinogen component and 0.062 Units/mg of fibrinogen component. Also disclosed are methods for treating wounded tissue.
Priority: US20060835423P Applic. Date: 2006-08-04
Inventor: MACPHEE MARTIN [US]; BEALL DAWSON [US]
Application No.: US20080038316A1 Published: 14/Feb/2008Title: Conveniently implantable sustained release drug compositions
Applicant/Assignee:
Application No.: 11/826833 Filing Date: 18/Jul/2007
Abstract:This invention provides for biocompatible and biodegradable syringeable liquid, implantable solid, and injectable gel pharmaceutical formulations useful for the treatment of systemic and local disease states.
Priority: US2005-236426 Applic. Date: 2005-09-27; US20050709665P Applic. Date: 2005-08-19; US20040614484P Applic. Date: 2004-10-01; US20060831991P Applic. Date: 2006-07-19
Inventor: WONG VERNON G [US]; WOOD LOUIS L [US]
Application No.: US20080038351A1 Published: 14/Feb/2008Title: Flowable carrier matrix
Applicant/Assignee: WARSAW ORTHOPEDIC, INC
Application No.: 11/504363 Filing Date: 14/Aug/2006
Abstract:A carrier matrix may be delivered to a target position within a patient in a minimally invasive manner by first cutting a collagen sponge sheet into a plurality of relatively small pieces. These pieces are sized so that, when wet, they are capable of flowing through a cannula and/or reduced-diameter syringe tip. The pieces are placed into a syringe and wetted, say with a morphogenic solution, and optionally mixed with a bulking material, which is similarly sized to fit through the cannula. The thoroughly mixed and wetted product forms a viscous aggregate which may then be injected into the patient at the target site.
Priority:
Inventor: BEALS NEAL [US]; SCIFERT JEFFREY L [US]; BODEN SCOTT D [US]
Application No.: US20080038764A1 Published: 14/Feb/2008Title: COMPOSITIONS, KIT AND ONE-STEP METHOD FOR MONITORING COMPOUNDS HAVING ANTI-FACTOR Xa AND/OR ANTI FACTOR IIa ACTIVITIES
Applicant/Assignee:
Application No.: 11/841684 Filing Date: 20/Aug/2007
Abstract:Provided are compositions and methods for accurate determination of the concentration of anticoagulant in a sample such as a blood or plasma sample. The compositions can contain a Factor X compound and Factor V compound, and additional components as well. Methods for performing the assay include one-step methods in which a sample is added to a coagulation assay composition, and time is monitored from the point of adding the sample and coagulation assay composition to an endpoint, such as clot formation.
Priority: US2005-127540 Applic. Date: 2005-05-11; US20040570312P Applic. Date: 2004-05-11
Inventor: YIN THYE [US]
Application No.: US20080038828A1 Published: 14/Feb/2008Title: Protocol for Monitoring Direct Thrombin Inhibition
Applicant/Assignee: HAEMOSCOPE CORPORATION
Application No.: 11/753071 Filing Date: 24/May/2007
Abstract:A hemostasis analyzer, such as the Thrombelastograph(R) (TEG(R)) hemostasis analyzer is utilized to measure continuously in real time, the hemostasis process from the initial fibrin formation, through platelet-fibrin interaction and lysis to generate blood hemostasis parameters. The measured blood hemostasis parameters permit evaluation of hemostasis therapies including anticoagulation therapies such as direct thrombin inhibition therapies.
Priority: US2006-608174 Applic. Date: 2006-12-07; US2003-384345 Applic. Date: 2003-03-07; US2000-591371 Applic. Date: 2000-06-09; US1999-255099 Applic. Date: 1999-02-22; US20060803184P Applic. Date: 2006-05-25
Inventor: COHEN ELI [US]; COHEN ROSLYN [US]
Application No.: US20080039373A1 Published: 14/Feb/2008Title: Pegylated Factor VII Glycoforms
Applicant/Assignee: NOVO NORDISK A/S
Application No.: 11/845175 Filing Date: 27/Aug/2007
Abstract:The invention concerns a preparation comprising a plurality of Factor VII polypeptides or Factor VII-related polypeptides, wherein the polypeptides comprise asparagine-linked and/or serine-linked oligosaccharide chains, and wherein at least one oligosaccharide group is covalently attached to at least one polymeric group.
Priority: DK20020000964 Applic. Date: 2002-06-21; US2003-609701 Applic. Date: 2003-06-30; WO2003DK00420 Applic. Date: 2003-06-20; US20020394778P Applic. Date: 2002-07-01
Inventor: KLAUSEN NIELS K [DK]; BJORN SOREN [DK]; BEHRENS CARSTEN [DK]; GARIBAY PATRICK W [DK]
Application No.: US20080045881A1 Published: 21/Feb/2008Title: DEVICES AND METHODS FOR REMOVING A MATTER FROM A BODY CAVITY OF A PATIENT
Applicant/Assignee: UNIVERSITY OF SOUTHERN CALIFORNIA
Application No.: 11/829879 Filing Date: 27/Jul/2007
Abstract:Disclosed are systems and methods for removing a matter from a body cavity of a patient. Exemplary systems of the present invention generally comprise a delivery catheter device, a central matter retrieval device and a device retriever. The central matter retrieval device has an elongated body and shape memory foam attached thereon. In use, the central matter retrieval device is housed within a parking segment of the delivery catheter and delivered to a desired body cavity in a patient. The retriever device is separately deployed to securely remove the matter and the central matter retrieval device from the patient.
Priority: US2005-087780 Applic. Date: 2005-03-23; WO2005US09658 Applic. Date: 2005-03-24; US20040556993P Applic. Date: 2004-03-26; US20040611684P Applic. Date: 2004-09-20; US20060820671P Applic. Date: 2006-07-28
Inventor: TEITELBAUM GEORGE P [US]; LARSEN DONALD W [US]
Application No.: US20080045985A1 Published: 21/Feb/2008Title: COMPOSITIONS AND METHODS FOR JOINING NON-CONJOINED LUMENS
Applicant/Assignee: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Application No.: 11/766779 Filing Date: 21/Jun/2007
Abstract:Disclosed are compositions, methods, and kits for joining together non-conjoined lumens in a patient's body including vascular lumens. More particularly, in various aspects, this invention provides compositions, methods, and kits for joining such non-conjoined lumens, including small lumens typically requiring microsurgical technique
Priority: US20060805425P Applic. Date: 2006-06-21; US20060806242P Applic. Date: 2006-06-29; US20070914635P Applic. Date: 2007-04-27
Inventor: GURTNER GEOFFREY C [US]; FULLER GERALD G [US]; LONGAKER MICHAEL T [US]; RAJADAS JAYAKUMAR [US]
Application No.: US20080047898A1 Published: 28/Feb/2008Title: Sealed Sterile System and Method for Filtering Biological or Medical Fluids, in Particular Whole Blood
Applicant/Assignee: GERATEZENTRALE FUR BLUTTRANSFUSION DES OSTERREICHI
Application No.: 11/632823 Filing Date: 14/Jun/2005
Abstract:The invention relates to a sealed, sterile system for filtering fluids, in particular whole blood. The system comprises a first collapsible container for receiving the fluid to be filtered and a second collapsible container for receiving the filtered fluid, both containers interconnected by a fluid line, in which a filter and a third container, for deaeration, are located. The first collapsible container contains a predetermined quantity of air, which is sufficient to ensure that no blood remains in the filter and the adjacent tube line sections when the whole blood is transferred from the first container into the second container. The air that is present in the second container, after the whole blood has been filtered, is transferred to the deaeration container.
Priority: DE200410035352 Applic. Date: 2004-07-21; WO2005EP06338 Applic. Date: 2005-06-14
Inventor: SOMMER CHRISTIAN [AT]; KURZ MICHAEL [AT]; MAYER GUNTER [AT]
Application No.: US20080047908A1 Published: 28/Feb/2008Title: Tool for Recovering Biological Samples and Method for Recovering Biological Samples
Applicant/Assignee: EIKEN KAGAKU KABUSHIKI KAISHA
Application No.: 11/597412 Filing Date: 25/May/2005
Abstract:This invention provides a tool for recovering biological samples for realizing more simple and accurate clinical testing with the use of a trace amount of the blood sample, a kit comprising the same, and a method for recovering and separating biological samples using the same. Such tool comprises: a recovery container body composed of an upper container portion having a medium-accommodating portion, provided with an upper opening, for accommodating and conserving an absorption medium to be impregnated with the recovered biological samples and a lower container portion for accommodating the biological samples separated from the medium
and a lid for closing the upper opening of the medium-accommodating portion, the bottom of such medium-accommodating portion being provided with an open area in communication with the lower container portion.
Priority: JP20040158290 Applic. Date: 2004-05-27; WO2005JP09534 Applic. Date: 2005-05-25
Inventor: SEKINE KAZUHITO [JP]; HIRAHARA SHIN [JP]; ICHIKAWA YOSHIHARU [JP]; TAKAHASHI TOMOYOSHI [JP]; OYAMA TAKAO [JP]; TAKAHASHI MASAMI [JP]
Application No.: US20080050389A1 Published: 28/Feb/2008Title: Compositions and methods for prevention and treatment of uncontrolled formation of intravascular fibrin clots
Applicant/Assignee: TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA UNIVERSITY OF VIRGINIA PATENT FOUNDATION
Application No.: 11/640737 Filing Date: 18/Dec/2006
Abstract:Compositions and methods for prevention and treatment of uncontrolled formation of intravascular fibrin clots are provided wherein fibrinolytic or anticoagulant drugs are biocompatibly coupled to red blood cell carriers.
Priority: US2002-253518 Applic. Date: 2002-09-23; US1999-454666 Applic. Date: 1999-12-03; WO1999US10547 Applic. Date: 1999-05-12; US19980086262P Applic. Date: 1998-05-21
Inventor: MUZYKANTOV VLADIMIR R [US]; HIGAZI ABD A [US]; MURCIANO JUAN C [ES]; CINES DOUGLAS [US]; TAYLOR RONALD P [US]
Application No.: US20080050394A1 Published: 28/Feb/2008Title: System and device for medically treating an individual
Applicant/Assignee:
Application No.: 11/507876 Filing Date: 22/Aug/2006
Abstract:A system for medically treating/vaccinating an individual comprising a first syringe, containing an anticoagulant material therein, for drawing a sample of blood from the individual. A centrifuge means for centrifuging the sample of blood contained within the first syringe to obtain a buffy coat. A second syringe comprising a second plunger and at least one microtubule member containing one of a treatment agent and a vaccine antigen. At least one open end formed within the at least one microtubule member for drawing a portion of the buffy coat therein and exposing the buffy coat to one of the treatment agent and vaccine antigen. A second needle capable of being attached onto the second syringe for introducing the exposed sample into the individual to effect treatment/vaccination thereof.
This system is capable of allowing a plurality of treatment agents and/or vaccine antigens to be simultaneously applied to an individual.
Priority:
Inventor: NALIN DAVID R [US]
Application No.: US20080050461A1 Published: 28/Feb/2008Title: NANOPARTICULATE COMPOSITIONS OF ANGIOGENESIS INHIBITORS
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 11/928250 Filing Date: 30/Oct/2007
Abstract:Nanoparticulate compositions comprising at least one poorly soluble angiogenesis inhibitor and at least one surface stabilizer are described. The nanoparticulate compositions have an average particle size of less than about 2000 nm. The invention also describes methods of making and using such compositions.
Priority: US2003-392403 Applic. Date: 2003-03-20; US20020365540P Applic. Date: 2002-03-20; US20020366542P Applic. Date: 2002-03-25
Inventor: MERISKO-LIVERSIDGE ELAINE [US]; BOSCH H WILLIAM [US]; CARY GRETA G [US]; PRUITT JOHN [US]; RYDE TUULA [US]; JAIN RAJEEV [US]; WALTERS AMY [US]
Application No.: US20080051689A1 Published: 28/Feb/2008Title: WEARABLE ULTRAFILTRATION DEVICE
Applicant/Assignee: NATIONAL QUALITY CARE, INC
Application No.: 11/933569 Filing Date: 01/Nov/2007
Abstract:An ultrafiltration device adapted to be worn on a portion of the body of a patient includes a blood inlet tube leading from a first blood vessel, a blood pump, an anticoagulant reservoir for infusing anticoagulants into the blood, a blood filter including a substrate through which the blood is circulated and filtered, a fluid bag for storing the excess fluid and a blood outlet tube leading to a second blood vessel.
Priority: US2004-846618 Applic. Date: 2004-05-17; US2001-085349 Applic. Date: 2001-11-16
Inventor: GURA VICTOR [US]; RAMBOD EDMOND [US]
Application No.: US20080056933A1 Published: 06/Mar/2008Title: Self-Propelled Sterilization Robot and Method
Applicant/Assignee:
Application No.: 11/468157 Filing Date: 29/Aug/2006
Abstract:A sterilization apparatus ( 200 ) comprises a robot ( 201 ), at least one germicidal energy source ( 202 ), and at least one motive capability ( 203 ). The sterilization apparatus may optionally further comprise numerous additional components, including a filtration unit ( 204 ), at least one power source ( 209 ), a power connector ( 210 ), an environmental sampling device ( 211 ), at least one sensor ( 212 ), a control system ( 213 ), an audio output device ( 214 ), a data transmitter ( 215 ), a global positioning satellite (GPS) receiver ( 216 ), a radio frequency identification (RFID) tag ( 217 ), a vacuum device ( 218 ), a floor washing device ( 219 ), an activator ( 220 ), a waterproof housing ( 221 ), and/or a padded housing ( 222 ).
Priority:
Inventor: MOORE BARRETT H [US]; BOTOS MATTHEW J [US]
Application No.: US20080057101A1 Published: 06/Mar/2008Title: MEDICAL DEVICES FOR CONTROLLED DRUG RELEASE
Applicant/Assignee:
Application No.: 11/839093 Filing Date: 15/Aug/2007
Abstract:The present invention is a medical device for controlling the release of an active agent. The medical device has a supporting structure having a porous body disposed therein. At least one elution rate controlling matrix containing an effective amount of at least one active agent is disposed within the pores of the porous body in a manner that protects the matrix from mechanical damage. The medical device may therefore be used for controlled drug release applications. Additionally, the present invention discloses a method for using the medical device for the treatment and prevention of diseases in mammals. This invention further relates to a method for using the medical device for treating and preventing vascular diseases.
Priority: US20060823057P Applic. Date: 2006-08-21; US20060823061P Applic. Date: 2006-08-21; US20060823063P Applic. Date: 2006-08-21; US20060823067P Applic. Date: 2006-08-21; US20060823069P Applic. Date: 2006-08-21; US20060823071P Applic. Date: 2006-08-21
Inventor: ROORDA WOUTER [US]
Application No.: US20080057102A1 Published: 06/Mar/2008Title: METHODS OF MANUFACTURING MEDICAL DEVICES FOR CONTROLLED DRUG RELEASE
Applicant/Assignee:
Application No.: 11/839104 Filing Date: 15/Aug/2007
Abstract:The present invention is a medical device for controlling the release of an active agent. The medical device has a supporting structure having a porous body disposed therein. At least one elution rate controlling matrix containing an effective amount of at least one active agent is disposed within the pores of the porous body in a manner that protects the matrix from mechanical damage. The medical device may therefore be used for controlled drug release applications. Additionally, the present invention discloses a method for using the medical device for the treatment and prevention of diseases in mammals. This invention further relates to a method for using the medical device for treating and preventing vascular diseases.
Priority: US20060823057P Applic. Date: 2006-08-21; US20060823061P Applic. Date: 2006-08-21; US20060823063P Applic. Date: 2006-08-21; US20060823067P Applic. Date: 2006-08-21; US20060823069P Applic. Date: 2006-08-21; US20060823071P Applic. Date: 2006-08-21; US2007-839093 Applic. Date: 2007-08-15; US2007-839121 Applic. Date: 2007-08-15
Inventor: ROORDA WOUTER [US]
Application No.: US20080057103A1 Published: 06/Mar/2008Title: METHODS OF USING MEDICAL DEVICES FOR CONTROLLED DRUG RELEASE
Applicant/Assignee:
Application No.: 11/839121 Filing Date: 15/Aug/2007
Abstract:The present invention is a medical device for controlling the release of an active agent. The medical device has a supporting structure having a porous body disposed therein. At least one elution rate controlling matrix containing an effective amount of at least one active agent is disposed within the pores of the porous body in a manner that protects the matrix from mechanical damage. The medical device may therefore be used for controlled drug release applications. Additionally, the present invention discloses a method for using the medical device for the treatment and prevention of diseases in mammals. This invention further relates to a method for using the medical device for treating and preventing vascular diseases.
Priority: US20060823057P Applic. Date: 2006-08-21; US20060823061P Applic. Date: 2006-08-21; US20060823063P Applic. Date: 2006-08-21; US20060823067P Applic. Date: 2006-08-21; US20060823069P Applic. Date: 2006-08-21; US20060823071P Applic. Date: 2006-08-21; US2007-839093 Applic. Date: 2007-08-15; US2007-839104 Applic. Date: 2007-08-15
Inventor: ROORDA WOUTER [US]
Application No.: US20080058695A1 Published: 06/Mar/2008Title: Autotransfusion Method and Autotransfusion Device with Phase Separation and Concentration, Comprising Removable Bags
Applicant/Assignee: DIRECTION ET PRIORITES SA
Application No.: 11/660323 Filing Date: 04/Aug/2005
Abstract:A process for treating the haemorrhage fluids of a patient at the time of a surgical procedure with the aim of carrying out an autotransfusion, includes a stage for recovering the haemorrhage fluids with simultaneous introduction of agents such as anticoagulant and/or diluting agents, at least one stage for the mechanical separation/concentration of this haemodiluted haemorrhage fluid in order to concentrate its content in red blood cells and partially purify it, this phase being collected in a sterile manner so as to be fit for injecting back to the patient. Also described is the related device.
Priority: WO2005FR50648 Applic. Date: 2005-08-04
Inventor: PEROVITCH PHILIPPE [FR]; GADRAT FRANCIS [FR]; CHASTENET BERTRAND [FR]
Application No.: US20080058696A1 Published: 06/Mar/2008Title: WEARABLE CONTINUOUS RENAL REPLACEMENT THERAPY DEVICE
Applicant/Assignee: NATIONAL QUALITY CARE, INC
Application No.: 11/933533 Filing Date: 01/Nov/2007
Abstract:A continuous renal replacement therapy (CRRT) device adapted to be worn on a portion of the body of a patient. The CRRT device is worn by the patient and operates on rechargeable batteries for more than 5 hours. Dialysate is used to remove impurities from the blood. The dialysate is recycled and refreshed by a filter section. Less than one liter of dialysate is required to circulate through the wearable CRRT device.
Priority: US2004-940862 Applic. Date: 2004-09-14; US2001-085349 Applic. Date: 2001-11-16
Inventor: GURA VICTOR [US]; RAMBOD EDMOND [US]
Application No.: US20080063695A1 Published: 13/Mar/2008Title: Thin film dressing
Applicant/Assignee: TYCO HEALTHCARE GROUP LP
Application No.: 11/900301 Filing Date: 11/Sep/2007
Abstract:Multi-layer articles are provided which are suitable for use as medical dressings. The articles include a hydrophilic layer, a hydrophobic layer, a delivery layer, and a release layer. In embodiments, the articles may also include adhesive tapes, stabilizer layers, and absorbent materials which may be included in an existing layer or applied as a separate absorbent layer.
Priority: US20060844008P Applic. Date: 2006-09-12
Inventor: VITARIS RONALD F [US]
Application No.: US20080063708A1 Published: 13/Mar/2008Title: Pharmaceutical Compositions of Amorphous Dispersions of Drugs and Lipophilic Microphase-Forming Materials
Applicant/Assignee:
Application No.: 11/924988 Filing Date: 26/Oct/2007
Abstract:A pharmaceutical composition comprises a solid amorphous dispersion comprising a low-solubility drug and a concentration-enhancing polymer and a lipophilic microphase-forming material. Alternatively, a solid amorphous dispersion comprising a low-solubility drug and a concentration-enhancing polymer is co-administered with a lipophilic microphase-forming material to an in vivo use environment.
Priority: WO2003IB00335 Applic. Date: 2003-01-28; US2003-355747 Applic. Date: 2003-01-31; US20020354081P Applic. Date: 2002-02-01
Inventor: PERLMAN MICHAEL E [US]; SHANKER RAVI M [US]; BABCOCK WALTER C [US]; FRIESEN DWAYNE T [US]; RABENSTEIN MARK D [US]; SMITHEY DAN T [US]
Application No.: US20080066741A1 Published: 20/Mar/2008Title: METHODS AND SYSTEMS OF DELIVERING MEDICATION VIA INHALATION
Applicant/Assignee:
Application No.: 11/689315 Filing Date: 21/Mar/2007
Abstract:Systems and methods for delivery of a drug to the respiratory system of a patient are provided, where the drug is supplied in purified air at a positive pressure relative to atmospheric pressure. With the systems and methods of the present disclosure, medication available in a variety of forms is introduced in a controlled fashion into the purified air stream in aerosol, nebulized, or vaporized form.
Priority: US2007-627692 Applic. Date: 2007-01-26; US2006-552871 Applic. Date: 2006-10-25; US20060826271P Applic. Date: 2006-09-20
Inventor: LEMAHIEU EDWARD [US]; JONES CHARLES [US]; STERN TOM [US]; HEBRANK JACK [US]; HUNTER CHARLES ERIC [US]; DUVALL LYNDELL [US]; HARTLEY CHRIS [US]; BALLOU BERNARD L [US]; HUNTER JOCELYN [US]; MCNEIL LAURIE [US]; WETZEL PAUL [US]; CRISS RON [US]
Application No.: US20080069889A1 Published: 20/Mar/2008Title: Compressible resilient granules and formulations prepared therefrom
Applicant/Assignee:
Application No.: 11/899601 Filing Date: 05/Sep/2007
Abstract:The present invention provides resilient self-adhering granules which comprise a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa.s to about 250,000 mPa.s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m<2>. The present invention also provides oral dosage compositions comprising the resilient self-adhering granules and methods for making and using the resilient self-adhering granules.
Priority: US2007-715821 Applic. Date: 2007-03-07; US20060780304P Applic. Date: 2006-03-07
Inventor: CHERUKURI S R [US]
Application No.: US20080075691A1 Published: 27/Mar/2008Title: Permucosal Composition and Method of Improving Permucosal Absorption
Applicant/Assignee: OTSUKA PHARMACEUTICAL CO., LTD
Application No.: 11/662094 Filing Date: 12/Sep/2005
Abstract:An object of the invention is to provide a composition for transmucosal administration that enables pharmacologically active peptides and proteins to be efficiently absorbed through the mucosa such as the pulmonary mucosa, nasal mucosa, oral mucosa, vaginal mucosa, gastric mucosa, gastrointestinal mucosa or the like. A composition for transmucosal administration are prepared by adding (i) at least one member selected from the group consisting of peptides and proteins having pharmacological activity
and (ii) at least one member selected from the group consisting of chitosan oligosaccharides having a polymerization degree of from 2 to 20, derivatives thereof, glucosamine, and salts thereof.
Priority: JP20040268891 Applic. Date: 2004-09-15; WO2005JP16739 Applic. Date: 2005-09-12
Inventor: YAMAMOTO AKIRA [JP]; YAMADA KEIGO [JP]
Application No.: US20080075772A1 Published: 27/Mar/2008Title: PHARMACEUTICAL COMPOSITIONS HAVING NOVEL SCORING PATTERNS AND METHODS OF USING THOSE COMPOSITIONS
Applicant/Assignee:
Application No.: 11/735268 Filing Date: 13/Apr/2007
Abstract:The invention provides novel scoring patterns for a wide variety of tablets that contain specific drugs or contain drugs in certain drug classes, and methods of treatment with layered tablets and fractional tablets derived from breaking said tablets.
Priority: US20060791834P Applic. Date: 2006-04-13; US20060792601P Applic. Date: 2006-04-17; US20060792933P Applic. Date: 2006-04-18; US20060861898P Applic. Date: 2006-11-30
Inventor: SOLOMON LAWRENCE [US]; KAPLAN ALLAN S [US]
Application No.: US20080075788A1 Published: 27/Mar/2008Title: DIAMMONIUM PHOSPHATE AND OTHER AMMONIUM SALTS AND THEIR USE IN PREVENTING CLOTTING
Applicant/Assignee:
Application No.: 11/859291 Filing Date: 21/Sep/2007
Abstract:The present invention relates to products, methods, and processes of various ammonium salts and their use as anti-coagulants.
Priority: US20060846312P Applic. Date: 2006-09-21
Inventor: LEE SAMUEL [US]; LOUIE STEPHANIE [US]; SCHWARDT JEFFREY D [US]; SLATER THOMAS A [US]; WENZ ROBERT [DE]
Application No.: US20080086107A1 Published: 10/Apr/2008Title: DEVICES FOR DELIVERING SUBSTANCES THROUGH AN EXTRA-ANATOMIC OPENING CREATED IN AN AIRWAY
Applicant/Assignee: BRONCUS TECHNOLOGIES, INC
Application No.: 11/538950 Filing Date: 05/Oct/2006
Abstract:Devices and methods for delivering substances to lung tissue through an extra-anatomic passage created in an airway.
Priority:
Inventor: ROSCHAK EDMUND J [US]
Application No.: US20080090800A1 Published: 17/Apr/2008Title: Mandelic acid derivatives and their use as thrombin inhibitors
Applicant/Assignee: ASTRAZENECA AB ASTRAZENECA
Application No.: 11/797656 Filing Date: 04/May/2007
Abstract:There is provided a compound of formula (I) wherein R, R<1>, R<2>, Y and R<3 >have meanings given in the description and pharmaceutically-acceptable derivatives (including prodrugs) thereof, which compounds and derivatives are useful as, or are useful as prodrugs of, competitive inhibitors of trypsin-like proteases, such as thrombin, and thus, in particular, in the treatment of conditions where inhibition of thrombin is required (e.g., thrombosis) or as anticoagulants.Priority: SE20000004458 Applic. Date: 2000-12-01; SE20010000965 Applic. Date: 2001-03-19; SE20010001239 Applic. Date: 2001-04-06; SE20010002921 Applic. Date: 2001-08-30; US2006-520063 Applic. Date: 2006-09-13; US2003-432411 Applic. Date: 2003-05-21; WO2001SE02657 Applic. Date: 2001-11-30
Inventor: INGHARDT TORD [SE]; JOHANSSON ANDERS [SE]; SVENSSON ARNE [SE]
Application No.: US20080090807A1 Published: 17/Apr/2008
Title: LACTAM-CONTAINING COMPOUNDS AND DERIVATIVES THEREOF AS FACTOR XA INHIBITORS
Applicant/Assignee: BRISTOL-MYERS SQUIBB COMPANY BRISTOL-MEYERS SQUIBB COMPANY
Application No.: 11/955678 Filing Date: 13/Dec/2007
Abstract:The present application describes lactam-containing compounds and derivatives thereof of Formula I: or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
Priority: US2005-198801 Applic. Date: 2005-08-05; US2004-850587 Applic. Date: 2004-05-20; US2002-245122 Applic. Date: 2002-09-17; US20010324165P Applic. Date: 2001-09-21; US20020402317P Applic. Date: 2002-08-09
Inventor: PINTO DONALD J P [US]; QUAN MIMI L [US]; ORWAT MICHAEL J [US]; LI YUN-LONG [US]; HAN WEI [US]; QIAO JENNIFER X [US]; LAM PATRICK Y S [US]; KOCH STEPHANIE L [US]
Application No.: US20080090907A1 Published: 17/Apr/2008Title: Crystal Comprising (2R)-2-Propyloctanoic Acid and Amine
Applicant/Assignee: ONO PHARMACEUTICAL CO., LTD
Application No.: 11/579071 Filing Date: 27/Apr/2005
Abstract:Crystals comprising (2R)-2-propyloctoic acid and an amine which retain the pharmacological effect of (2R)-2-propyloctoic acid and can be safely used as a medicinal raw drug for peroral solid preparations. Of these crystals, the crystals especially with dibenzylamine are advantageous because not only the crystals themselves are useful as a medicinal raw drug but also use of the crystals as an intermediate can yield (2R)-2-propyloctoic acid having an optical purity exceeding 99.5% e.e., which has not been obtained hitherto.
Priority: JP20040134655 Applic. Date: 2004-04-28; WO2005JP08462 Applic. Date: 2005-04-27
Inventor: HASEGAWA TOMOYUKI [JP]; KAWANAKA YASUFUMI [JP]; KASAMATSU EIJI [JP]
Application No.: US20080097241A1 Published: 24/Apr/2008Title: SAMPLING DEVICE
Applicant/Assignee: CALIFORNIA INSTITUTE OF TECHNOLOGY
Application No.: 11/874830 Filing Date: 18/Oct/2007
Abstract:This invention provides devices and methods for obtaining a sample.
Priority: US20060852830P Applic. Date: 2006-10-18
Inventor: MALTEZOS GEORGE [US]; SCHERER AXEL [US]
Application No.: US20080097242A1 Published: 24/Apr/2008Title: Disposable Blood Sampling Device
Applicant/Assignee: KUN SHAN MEDSAFE MEDICAL TECH CO., LTD
Application No.: 11/781237 Filing Date: 21/Jul/2007
Abstract:A disposable blood sampling device is disclosed herein, which includes a plunger, a rubber stopper, a barrel, a sealing member, a needle holder, a protection sleeve, an anticoagulant storing tube and a needle sheath. In use, the disposable blood sampling device is deconstructed by removing each component therefrom and is unable to be assembled again for recycling. Furthermore, the needle can be hidden in the protection sleeve before it is detached from the blood sampling device, which effectively prevents a medical operator from being hurt or even infected by the needle.
Priority: TW20060218599U Applic. Date: 2006-10-20
Inventor: CAI JIAN [CN]
Application No.: US20080097243A1 Published: 24/Apr/2008Title: HOLLOW NEEDLE ASSEMBLY
Applicant/Assignee:
Application No.: 11/466588 Filing Date: 23/Aug/2006
Abstract:Some embodiments of the invention provide a needle with a sharp open end and a blunt open end, housed in a barrel with an open anterior end and an open posterior end. The barrel can travel along the hub of the needle, for extending the needle for insertion into a blood vessel, and for retracting the needle into the barrel to avoid injury. The blunt open end can be fluidly connected to the inlet opening of a measurement apparatus, so that the blood can flow directly into the measurement apparatus, eliminating the traditional step of transferring the blood from a syringe to the measurement apparatus. The hollow needle assembly can remain attached to the measurement apparatus because of its small size, and the engagement of an optional safety cap to the open anterior end of the barrel, minimizes the risk of injury and blood contamination. Because a small blood sample is required, a very small needle shaft can be used, minimizing the discomfort experienced by the patient.
Priority:
Inventor: SAMSOONDAR JAMES [CA]
Application No.: US20080097592A1 Published: 24/Apr/2008Title: Artificial Blood Vessel
Applicant/Assignee: VASCUTEK LIMITED TERUMO CORPORATION
Application No.: 11/792498 Filing Date: 14/Feb/2005
Abstract:There is described an artificial blood vessel for use in a region of a living body which needs to be repeatedly pierced with a needle. The artificial blood vessel includes a main section having a vessel wall which includes a laminated assembly comprising an inner layer, an outer layer, and an intermediate layer positioned therebetween, and a pair of anastomotic sections disposed on the respective opposite ends of the main section. Each of the anastomotic sections has an intermediate layer thinner than the intermediate layer of the main section or is free of an intermediate layer, so that the anastomotic section as a vessel wall thinner than the main section.
Priority: WO2005GB00521 Applic. Date: 2005-02-14
Inventor: FITZPATRICK CHARLES [GB]; OKUBO TADANORI [GB]
Application No.: US20080102115A1 Published: 01/May/2008Title: Modified coagulation factor IX polypeptides and use thereof for treatment
Applicant/Assignee:
Application No.: 11/818985 Filing Date: 15/Jun/2007
Abstract:Provided are modified factor IX (FIX) polypeptides and methods of generating modified FIX polypeptides. Also provided are pharmaceutical compositions, including compositions formulation for oral administration, that contain the modified FIX polypeptides, and methods of treatment using modified FIX polypeptides.
Priority: US20060815113P Applic. Date: 2006-06-19
Inventor: OYHENART JORGE [AR]; GALLET XAVIER [FR]; BORRELLY GILLES [FR]; GUYON THIERRY [FR]; VEGA MANUEL [FR]; DRITTANTI LILA [FR]
Application No.: US20080107678A1 Published: 08/May/2008Title: Method for treating thrombotic disorders using sulfated polysaccharides
Applicant/Assignee:
Application No.: 11/789447 Filing Date: 24/Apr/2007
Abstract:Methods for treating thrombotic disorders using sulfated polysaccharides such as fucoidans are disclosed.
Priority: US20060797079P Applic. Date: 2006-04-27
Inventor: JOHNSON KIRK W [US]
Application No.: US20080107741A1 Published: 08/May/2008Title: NANOPARTICULATE COMPOSITIONS OF ANGIOGENESIS INHIBITORS
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 11/928278 Filing Date: 30/Oct/2007
Abstract:Nanoparticulate compositions comprising at least one poorly soluble angiogenesis inhibitor and at least one surface stabilizer are described. The nanoparticulate compositions have an average particle size of less than about 2000 nm. The invention also describes methods of making and using such compositions.
Priority: US2003-392403 Applic. Date: 2003-03-20; US20020366542P Applic. Date: 2002-03-25; US20020365540P Applic. Date: 2002-03-20
Inventor: MERISKO-LIVERSIDGE ELAINE [US]; BOSCH H W [US]; CARY GRETA G [US]; PRUITT JOHN [US]; RYDE TUULA [US]; JAIN RAJEEV [US]; WALTERS AMY [US]
Application No.: US20080108122A1 Published: 08/May/2008Title: Microchemical nanofactories
Applicant/Assignee: STATE UNIVERSITY
Application No.: 11/897998 Filing Date: 31/Aug/2007
Abstract:Embodiments of an apparatus, system, and method for chemical synthesis and/or analysis are disclosed. One embodiment of a disclosed apparatus comprises a laminated, microfluidic structure defining a reactor and a separator. Such apparatuses, or portions thereof, generally have dimensions ranging from about 1 micrometer to about 100 micrometers. To implement synthetic processes, disclosed embodiments of the apparatus generally include at least one unit operation, such as a mixer, a valve, a separator, a detector, and combinations thereof. Individual apparatuses may be coupled both in series and in parallel to form a system for making chemical compounds. An individual apparatus or a system also can be used in combination with known devices and processes.
Priority: US20060841778P Applic. Date: 2006-09-01
Inventor: PAUL BRIAN K [US]; CHANG CHIH-HUNG [US]; REMCHO VINCENT T [US]
Application No.: US20080108942A1 Published: 08/May/2008Title: ANALYTE SENSOR
Applicant/Assignee: DEXCOM, INC
Application No.: 11/691426 Filing Date: 26/Mar/2007
Abstract:Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes a vascular access device, a sensor and sensor electronics, the system being configured for insertion into communication with a host's circulatory system.
Priority: US2006-543396 Applic. Date: 2006-10-04; US2006-543490 Applic. Date: 2006-10-04; US2006-543404 Applic. Date: 2006-10-04
Inventor: BRISTER MARK [US]; SWANSON VANCE [US]; PETISCE JAMES R [US]; SAINT SEAN [US]; WONG DAVID K [US]; WOO KUM MING [US]
Application No.: US20080109070A1 Published: 08/May/2008Title: BIODEGRADABLE ELASTOMERIC SCAFFOLDS CONTAINING MICROINTEGRATED CELLS
Applicant/Assignee:
Application No.: 11/837235 Filing Date: 10/Aug/2007
Abstract:Described herein are elastomeric materials, and in particular porous biodegradable elastomeric materials which optionally may have microintegrated cells. Also described herein are bioprosthetic devices that can be manufactured using the biodegradable elastomeric materials, non-limiting examples of such devices including pulmonary valves, vocal chords, and blood vessels.
Priority: US20060822073P Applic. Date: 2006-08-10
Inventor: WAGNER WILLIAM R [US]; STANKUS JOHN [US]; GUAN JIANJUN [US]; FUJIMOTO KAZURO L [US]; NIEPONICE ALEJANDRO [AR]; SOLETTI LORENZO [US]; VORP DAVID A [US]; SACKS MICHAEL S [US]; COURTNEY TODD [US]; MAYER JOHN E [US]
Application No.: US20080112955A1 Published: 15/May/2008Title: METHOD AND COMPOSITION FOR PREVENTING PAIN IN SICKLE CELL PATIENTS
Applicant/Assignee: TRF PHARMA, INC
Application No.: 12/015885 Filing Date: 17/Jan/2008
Abstract:A method of preventing pain in a sickle cell patient is disclosed. The method includes orally administering to the patient, an amount of an active agent effective on oral administration to inhibit binding of the patient's sickle erythrocytes to P-selectin on the patient's vascular endothelium. The inhibition may be evidenced in a number of ways. The active agent administration inhibits the adhesion of sickle erythrocytes to vascular endothelium in the patient, thereby preventing patient pain associated with vascular occlusion. Also disclosed are compositions useful in practicing the method.
Priority: US2003-418653 Applic. Date: 2003-04-18; US20020373841P Applic. Date: 2002-04-18; US20020373842P Applic. Date: 2002-04-18; US20020373844P Applic. Date: 2002-04-18
Inventor: EMBURY STEPHEN H [US]; MATSUI NEIL M [US]
Application No.: US20080119703A1 Published: 22/May/2008Title: Analyte sensor
Applicant/Assignee:
Application No.: 11/543396 Filing Date: 04/Oct/2006
Abstract:Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes a vascular access device, a sensor and sensor electronics, the system being configured for insertion into a host's peripheral vein or artery.
Priority: US2006-543404 Applic. Date: 2006-10-04; US2006-543490 Applic. Date: 2006-10-04
Inventor: BRISTER MARK [US]; SAINT SEAN [US]; SWANSON VANCE [US]; PETISCE JAMES R [US]
Application No.: US20080119704A1 Published: 22/May/2008Title: Analyte sensor
Applicant/Assignee:
Application No.: 11/543490 Filing Date: 04/Oct/2006
Abstract:Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes a vascular access device, a sensor and sensor electronics, the system being configured for insertion into a host's peripheral vein or artery.
Priority: US2006-543396 Applic. Date: 2006-10-04; US2006-543404 Applic. Date: 2006-10-04
Inventor: BRISTER MARK [US]; SAINT SEAN [US]; SWANSON VANCE [US]; QUINTANA NELSON [US]
Application No.: US20080124280A1 Published: 29/May/2008Title: Thyroid Hormone Analogs and Methods of Use
Applicant/Assignee:
Application No.: 11/663047 Filing Date: 15/Sep/2005
Abstract:Disclosed are methods of treating subjects having conditions related to angiogenesis including administering an effective amount of a polymeric form of thyroid hormone, or an antagonist thereof, to promote or inhibit angiogenesis in the subject. Compositions of the polymeric forms of thyroid hormone, or thyroid hormone analogs, are also disclosed.
Priority: US2004-943072 Applic. Date: 2004-09-15; US20030502721P Applic. Date: 2003-09-15; US20050670534P Applic. Date: 2005-04-13; WO2005US32813 Applic. Date: 2005-09-15
Inventor: MOUSA SHAKER A [US]; DAVIS FAITH B [US]; DAVIS PAUL J [US]
Application No.: US20080124700A1 Published: 29/May/2008Title: Method and apparatus for controlling the flow rate of washing solution during the washing step in a blood centrifugation bowl
Applicant/Assignee:
Application No.: 11/604664 Filing Date: 27/Nov/2006
Abstract:A method of washing blood mixed with undesirable elements not normally found in healthy whole blood to remove the undesirable elements, the method comprising: separating the blood into components according to relative densities of the components with a rotating centrifuge bowl
providing a port through which fluid exits the bowl, the exiting fluid having a concentration of undesirable elements
flowing washing solution into the centrifuge bowl at an initial flow rate
monitoring the fluid exiting the bowl with an optical sensor having an output signal indicative of the composition of the exiting fluid
and increasing and decreasing the flow rate of the wash solution as a function of the output signal.
Priority:
Inventor: FORTINI MATTEO [IT]; REGGIANI STEFANO [IT]; PANZANI IVO [IT]
Application No.: US20080131423A1 Published: 05/Jun/2008Title: Anti-TREM-like transcript-1 (TLT-1) antibodies, methods and compositions
Applicant/Assignee: GOVERNMENT OF THE US, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES THE UNITED STATES OF AMERICA AS REPRESENTED BY SECRETARY DEPARTMENT OF HEALTH AND HUMAN SERVICES
Application No.: 11/634331 Filing Date: 04/Dec/2006
Abstract:The present invention relates to methods and compositions for modulating platelet activity, and methods and compositions for treating a disease or disorder associated with platelet activity in a subject, comprising administering a single chain anti-TREM-like transcript-1 (TLT-1) antibody or a functional fragment or variant thereof in an amount effective to modulate platelet activity.
Priority:
Inventor: MORI TOSHIYUKI [JP]; MCVICAR DANIEL W [US]; GIOMARELLI BARBARA [US]; WASHINGTON A V [US]
Application No.: US20080132499A1 Published: 05/Jun/2008Title: PLATELET ADP RECEPTOR INHIBITORS
Applicant/Assignee: PORTOLA PHARMACEUTICALS, INC
Application No.: 11/856616 Filing Date: 17/Sep/2007
Abstract:Compounds are provided which are useful as platelet ADP receptor inhibitors, for treating thrombosis and for reducing the likelihood and/or severity of a secondary ischemic event in a patient.
Priority: US20060846328P Applic. Date: 2006-09-20
Inventor: SCARBOROUGH ROBERT M [US]; SCARBOROUGH CARROLL ANNA CREW [US]; BAUER SHAWN M [US]; PANDEY ANJALI [US]
Application No.: US20080138277A1 Published: 12/Jun/2008Title: Delivery systems and methods for diagnosing and treating cardiovascular diseases
Applicant/Assignee: MEDSTAR HEALTH INC GEORGETOWN UNIVERSITY
Application No.: 11/386513 Filing Date: 23/Mar/2006
Abstract:The invention relates to the treatment and prevention of atherosclerosis and cardiovascular diseases associated with atherosclerosis. The invention further relates to methods of diagnosing atherosclerosis and cardiovascular diseases associated with atherosclerosis. In certain embodiments, the invention provides biological systems and methods for delivering a therapeutic agent or an imaging agent to atherosclerotic lesions such as vulnerable plaques.
Priority: US20050664330P Applic. Date: 2005-03-23
Inventor: EPSTEIN STEPHEN E [US]; BURNETT MARY SUSAN [US]; MULLINS MARTIN A [US]
Application No.: US20080145423A1 Published: 19/Jun/2008Title: Chewable tablet and method of formulating
Applicant/Assignee:
Application No.: 11/639016 Filing Date: 14/Dec/2006
Abstract:Processes for preparing a chewable tablet comprising a micronized form of an active ingredient, the method comprising the steps of combining the active ingredient with tablet excipients by geometric dilution to form a final mixture and applying direct compression to at least a portion of the final mixture to form at least one tablet.
Priority:
Inventor: KHAN AJMAL ALI [US]; BRUNSON EDDIE [US]
Application No.: US20080145438A1 Published: 19/Jun/2008Title: Micro- and nano-particulate drugs and methods of making thereof
Applicant/Assignee:
Application No.: 11/823476 Filing Date: 26/Jun/2007
Abstract:A micro and nano-particulate drug comprising a drug substance and a surfactant in which the drug and surfactant form a eutectic mixture. The matrix formed between the drug substance and the surfactant has a melting point less than the decomposition temperature of the drug substance and thus provides the advantages of reduced irritation due to the melting process without the prior art problem of decomposition of the drug substance. In one embodiment, crystals are formed while the mixture is cooled at room temperature under high shear conditions. In a second embodiment, a flowable material may be formed which also contains the drug and that may be incorporated into a pharmaceutical delivery system is also disclosed. Methods of preparing the micro and nano-particulate drug crystals and non-crystalline substance are also contemplated in the inventive subject matter.
Priority: US2001-022799 Applic. Date: 2001-12-20
Inventor: BOGUE BEUFORD ARLIE [US]
Application No.: US20080152585A1 Published: 26/Jun/2008Title: Low viscosity liquid dosage forms
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 11/979253 Filing Date: 31/Oct/2007
Abstract:The present invention relates to liquid dosage forms of nanoparticulate active agents having very low viscosities.
Priority: US2003-420927 Applic. Date: 2003-04-23; US2003-412669 Applic. Date: 2003-04-14; US20020371680P Applic. Date: 2002-04-12; US20020430348P Applic. Date: 2002-12-03
Inventor: RYDE TUULA [US]; RYDE NIELS [US]; BOSCH H WILLIAM [US]; PRUITT JOHN D [US]; WERTZ CHRISTIAN F [US]
Application No.: US20080153152A1 Published: 26/Jun/2008Title: MICROFLUIDIC CHIP
Applicant/Assignee:
Application No.: 11/943380 Filing Date: 20/Nov/2007
Abstract:A microfluidic chip, includes: a first port for inputting: a sample liquid
and a first liquid
a second port for inputting a second liquid
a third port for supplying air pressure
a first channel (A) for mixing the sample liquid and the first liquid to generate a first mixed liquid
a second channel (B) for beating the first mixed liquid
a third channel (C) for allowing the second liquid to converge into the first mixed liquid to generate a second mixed liquid
a fourth channel (D) installing a first solid
a fifth channel (E) for promoting mixing of the first solid
a plurality of sixth channels (F) each having a second solid
and a seventh channel (G), which connects the fifth channel (E) and the plurality of sixth channels (F), for dispensing a fixed quantity of the second mixed liquid to each of the plurality of sixth channels (F).
Priority: JP20060316129 Applic. Date: 2006-11-22; JP20070297003 Applic. Date: 2007-11-15
Inventor: WAKABAYASHI AKIRA [JP]; KARAKI HIDEYUKI [JP]; SAWAYASHIKI YOSHIHIRO [JP]; KATO KOTA [JP]; IWAKI YOSHIHIDE [JP]
Application No.: US20080154181A1 Published: 26/Jun/2008Title: Central nervous system ultrasonic drain
Applicant/Assignee:
Application No.: 12/008611 Filing Date: 11/Jan/2008
Abstract:The invention provides a method and apparatus for treating hemorrhage and maintaining catheter patency in the brain and spine through a new and minimally invasive technique. Ultrasound energy is delivered either through a catheter inserted directly into the hemorrhage and the delivered ultrasound energy dissolves the blood clot which is then drained through the catheter.
Priority: US2006-418849 Applic. Date: 2006-05-05
Inventor: KHANNA ROHIT K [US]
Application No.: US20080159984A1 Published: 03/Jul/2008Title: Compositions Capable of Facilitating Penetration Across a Biological Barrier
Applicant/Assignee:
Application No.: 11/547568 Filing Date: 14/Apr/2005
Abstract:This invention relates to novel penetrating compositions including one or more effectors included within a water soluble composition, immersed in a hydrophobic medium The invention also relates to methods of treating or preventing diseases by administering such penetrating compositions to affected subjects.
Priority: US20040562345P Applic. Date: 2004-04-15; WO2005IB04183 Applic. Date: 2005-04-14
Inventor: BEN-SASSON SHMUEL A [IL]
Application No.: US20080161296A1 Published: 03/Jul/2008Title: Compositions comprising nebivolol
Applicant/Assignee: FOREST LABORATORIES HOLDINGS LIMITED
Application No.: 11/273992 Filing Date: 15/Nov/2005
Abstract:Nebivolol has been shown to be beneficial in the treatment of cardiovascular diseases such hypertension, congestive heart failure, arterial stiffness and endothelial dysfunction. The present invention features a pharmaceutical composition comprising nebivolol and at least one other active agent, wherein the at least one other active agent is a cardiovascular agent.
Priority: US2005-141235 Applic. Date: 2005-05-31; US20040577423P Applic. Date: 2004-06-04
Inventor: DAVIS ERIC [US]; O'DONNELL JOHN P [US]; BOTTINI PETER BRUCE [US]; SHAW ANDREW [US]; MASON R PRESTON [US]
Application No.: US20080161793A1 Published: 03/Jul/2008Title: Cooled ablation catheter with reciprocating flow
Applicant/Assignee:
Application No.: 11/646255 Filing Date: 28/Dec/2006
Abstract:The invention relates to an ablation catheter which controls the temperature and reduces the coagulation of biological fluids on an electrode of a catheter, prevents the impedance rise of tissue in contact with the electrode, and maximizes the potential energy transfer to the tissue, thereby allowing an increase in the lesion size produced by the ablation. The electrode includes passages positioned to allow blood and other biological fluids to flow into and out of an inner cavity of the electrode. This fluid flow produced the desired cooling effect and is accomplished, for example, by a reciprocating plunger or piston, or by a balloon that is alternately inflated and deflated.
Priority:
Inventor: WANG HUISUN [US]; DANDO JEREMY D [US]
Application No.: US20080161907A1 Published: 03/Jul/2008Title: Stent coated with a sustained-release drug delivery and method for use thereof
Applicant/Assignee: PSIVIDA INC
Application No.: 11/906765 Filing Date: 02/Oct/2007
Abstract:An intraluminal medical device comprises a stent having a coating applied to at least part of an interior surface, an exterior surface, or both. The coating comprises a sustained release formulation of a combination of pharmaceutical compounds dispersed within a biologically tolerated polymer composition. The choice of the combination of pharmaceutical compounds are intended to reduce neointimal hyperplasia restenosis.
Priority: US2002-245840 Applic. Date: 2002-09-17; US20010322428P Applic. Date: 2001-09-17; US20020372761P Applic. Date: 2002-04-15
Inventor: CHEN JIANBING [US]; ASHTON PAUL [US]
Application No.: US20080166324A1 Published: 07/Dec/2006Title: PLASMA-DEPLETED, NON-RED BLOOD CELL-DEPLETED CORD BLOOD COMPOSITIONS AND METHODS OF USE
Applicant/Assignee: STEMCYTE, INC
Application No.: 11/422017 Filing Date: 02/Jun/2006
Abstract:The umbilical cord blood (UCB) compositions of the present invention possess the unique features of having plasma that is substantially depleted from the UCB unit and red blood cells (RBC) that are not depleted from the UCB unit. Such UCB units can be prepared by a process that combines plasma depletion with cryopreservation, selection, thawing, and/or transplantation of hematopoietic stem cells to provide superior clinical outcome by maximizing post-processing cell recovery and post-thaw infusion cell dose. Methods for treating a wide variety of malignant diseases and benign diseases associated with the hematopoietic system by administering the UCB compositions of the present invention are also provided.
Priority: US2003-367339 Applic. Date: 2003-02-13; US20050733956P Applic. Date: 2005-11-03; US20050687127P Applic. Date: 2005-06-02; US20020357308P Applic. Date: 2002-02-14
Inventor: CHOW ROBERT [US]
Application No.: US20080166390A1 Published: 10/Jul/2008Title: Biodegradable polyphosphazenes containing pyrrolidone side groups
Applicant/Assignee:
Application No.: 11/974528 Filing Date: 12/Oct/2007
Abstract:Biodegradable polyphosphazene polymers containing pyrrolidone side groups, and the biomedical use of such polyphosphazene polymers are disclosed.
Priority: WO2006US13661 Applic. Date: 2006-04-11
Inventor: ANDRIANOV ALEXANDER K [US]; MARIN ALEXANDER [US]
Application No.: US20080171972A1 Published: 17/Jul/2008Title: Medical device package
Applicant/Assignee:
Application No.: 11/544503 Filing Date: 06/Oct/2006
Abstract:The present disclosure provides a medical device package including a container for receiving a medical device having an area configured for storing at least one agent and a port for permitting the passage of a contact material between the outside the container and the area configured for storing the agent.
Priority:
Inventor: STOPEK JOSHUA B [US]
Application No.: US20080175831A1 Published: 24/Jul/2008Title: NEUROPROTECTION BY BLOOD FLOW STABILIZATION
Applicant/Assignee:
Application No.: 11/961835 Filing Date: 20/Dec/2007
Abstract:A treatment is disclosed for alleviation or prevention of abnormal blood flow to various organs such as the eye, brain, kidneys, heart, feet and other tissues of organs with fine vascular networks that can lead to neurodegeneration as is seen in wet age-related macular degeneration (AMD), epilepsy and diabetes, in which an effective amount of a blood flow regulatory drug is administered to a subject in need of it. Illustrative blood flow regulatory drugs include anticoagulants and vasodilators, and their mixtures.
Priority: US20060876354P Applic. Date: 2006-12-21; US20070977501P Applic. Date: 2007-10-04
Inventor: MACKNIK STEPHEN L [US]; MARTINEZ-CONDE SUSANA [US]
Application No.: US20080175878A1 Published: 24/Jul/2008Title: Protease for activating clotting factor VII
Applicant/Assignee: CSL BEHRING GMBH
Application No.: 11/984058 Filing Date: 13/Nov/2007
Abstract:A protease for activating the blood clotting factor VII is described, which (a) is inhibited by the presence of aprotinin, (b) is increased in its activity by calcium ions and/or heparin or heparin-related substances, and (c) in SDS-PAGE, on subsequent staining in the non-reduced state, comprises one or more bands in the molecular weight range from 50 to 75 kDa
and in SDS-PAGE, on subsequent staining in the reduced state, comprises a band at 40 to 55 kDa, one or more bands in the molecular weight range from 10 to 35 kDa, and a band, which corresponds to a proenzyme, in the molecular weight range between 60 and 65 kDa.
Priority: DE19981018495 Applic. Date: 1998-04-24; DE19981027734 Applic. Date: 1998-06-22; DE19981051332 Applic. Date: 1998-11-06; DE19981051335 Applic. Date: 1998-11-06; DE19981051336 Applic. Date: 1998-11-06; DE19991003693 Applic. Date: 1999-02-01; US2005-118396 Applic. Date: 2005-05-02; US2002-319592 Applic. Date: 2002-12-16; US1999-295316 Applic. Date: 1999-04-21
Inventor: ROMISCH JURGEN [DE]; FEUSSNER ANNETTE [DE]; STOHR HANS-ARNOLD [DE]
Application No.: US20080188400A1 Published: 07/Aug/2008Title: Methods For Treating Bleeding
Applicant/Assignee: MAXYGEN HOLDINGS LTD
Application No.: 11/912484 Filing Date: 25/Apr/2006
Abstract:Methods for the treatment of various bleeding disorders using variants of human Factor VII (hFVII) or activated FVII (FVIIa) having an altered activity compared to 5 recombinant FVIIa with the native human sequence.
Priority: US20050674815P Applic. Date: 2005-04-26; WO2006DK50016 Applic. Date: 2006-04-25
Inventor: ROPKE MADS [DK]; LATHROP STEPHANIE J [US]
Application No.: US20080190857A1 Published: 14/Aug/2008Title: System and Methods of Producing Membranes
Applicant/Assignee: CASCADE MEDICAL ENTRPRISES, LLC
Application No.: 11/909191 Filing Date: 22/Mar/2006
Abstract:An apparatus and method of forming a solid-fibrin web. The apparatus includes a centrifuge ( 600 ) having a housing ( 604 ), and actuator ( 648 ), a wheel ( 660 ), and a flange ( 664 ). The housing includes a recessed area ( 616 ) and a base ( 608 ) supportable on a surface. The wheel is coupled to the actuator and extends into the recessed area and is adapted to contact a first end of a container ( 620 ). The flange extends into the recessed area opposite the wheel and defines an adjustable distance between the wheel and the flange. The flange is adapted to contact a second end of the container and the actuator is operable to rotate the container. The container is oriented substantially parallel with respect to the base.
Priority: US20050664004P Applic. Date: 2005-03-22; WO2006US10525 Applic. Date: 2006-03-22
Inventor: BERETTA ROBERTO [IT]; GRIPPI NICHOLAS A [US]
Application No.: US20080193414A1 Published: 14/Aug/2008Title: Use of an Immunoglobulin Domain-Containing Cell Surface Recognition Molecule For Treating Diseases
Applicant/Assignee:
Application No.: 11/913620 Filing Date: 04/May/2006
Abstract:The invention relates to the use of INSP052 for treatment and/or prevention of infectious disease, properdin-related disease, MBL2-related disease, MASP1-related disease, MASP2-related disease, Antithrombin III-related disease, Complement factor H-related disease and/or Albumin-related disease. Combinations of INSP052 with an interferon, a TNF antagonist or a further anti-infectious or anti-blood clotting agent are also within the present invention.
Priority: EP20050103791 Applic. Date: 2005-05-06; US20050681651P Applic. Date: 2005-05-17; WO2006EP62063 Applic. Date: 2006-05-04
Inventor: PROUDFOOT AMANDA [FR]; ANTONSSON BRUNO [FR]; KONTULA LINDA [CH]; VILBOIS FRANCIS [FR]
Application No.: US20080194036A1 Published: 14/Aug/2008Title: Method For Determining Coagulation Activation And Device For Carrying Out Said Method
Applicant/Assignee: TECHNOCLONE GESELLSCHAFT M.B.H
Application No.: 11/884966 Filing Date: 22/Feb/2006
Abstract:The invention relates to a method for determining the generation of thrombin or factor Xa, said generation of activated coagulation factors in various sample materials, such as whole blood or plasma with different thrombocyte quantities, being triggered by phospholipid micelles with different tissue factor contents (0 to 1000 pM). According to the invention, the generation of thrombin is determined in a coagulation machine, which can simultaneously determine classic conventional coagulation parameters. The device for carrying out the method for the parallel determination of thrombin generation and classic conventional coagulation parameters has a rotating cuvette plate, into which a cuvette ring and cuvette elements are inserted.
According to the invention, at least one section of the cuvette ring contains a test station for at least two fluorescent test sets and at least four conventional test sets for coagulation, chromogenic substrates and turbidimetric analysis.
Priority: AT20050000296 Applic. Date: 2005-02-22; AT20050001656 Applic. Date: 2005-10-11; WO2006AT00073 Applic. Date: 2006-02-22
Inventor: BINDER BERND [AT]
Application No.: US20080194868A1 Published: 14/Aug/2008Title: HYDRODYNAMIC CAVITATION CRYSTALLIZATION DEVICE AND PROCESS
Applicant/Assignee:
Application No.: 11/782299 Filing Date: 24/Jul/2007
Abstract:A device and process for crystallizing a compound using hydrodynamic cavitation comprising the steps of mixing at least one stream of a solution of such compound to be crystallized with at least one stream of an anti-solvent and passing the mixed streams at an elevated pressure through a local constriction of flow to create hydrodynamic cavitation thereby causing nucleation and the direct production of crystals. The compound to be crystallized can be, for example, an active pharmaceutical ingredient.
Priority: US2006-330473 Applic. Date: 2006-01-12; US2003-382117 Applic. Date: 2003-03-04
Inventor: KOZYUK OLEG V [US]
Application No.: US20080195062A1 Published: 14/Aug/2008Title: SAMPLING OF BLOOD ANALYTES
Applicant/Assignee: VANDERBILT UNIVERSITY
Application No.: 11/422748 Filing Date: 07/Jun/2006
Abstract:The present invention provides for devices and methods of sampling and analyzing body fluid analytes, including proteins, nucleic acids, drugs, carbohydrates and lipids. Body fluids include blood, serum, sputum, saliva, urine, cerebrospinal fluid, and ascites.
Priority: US20050688618P Applic. Date: 2005-06-08; US20050711019P Applic. Date: 2005-08-24
Inventor: CAPRIOLI RICHARD [US]
Application No.: US20080197024A1 Published: 21/Aug/2008Title: ANALYTE SENSOR
Applicant/Assignee: DEXCOM, INC
Application No.: 12/055078 Filing Date: 25/Mar/2008
Abstract:Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes a vascular access device, a sensor and sensor electronics, the system being configured for insertion into communication with a host's circulatory system.
Priority: US2007-691466 Applic. Date: 2007-03-26; US2007-691424 Applic. Date: 2007-03-26; US2007-691432 Applic. Date: 2007-03-26; US2007-691426 Applic. Date: 2007-03-26; US2006-543396 Applic. Date: 2006-10-04; US2006-543490 Applic. Date: 2006-10-04; US2006-543404 Applic. Date: 2006-10-04; US2006-543683 Applic. Date: 2006-10-04; US2004-004561 Applic. Date: 2004-12-03; US2007-865572 Applic. Date: 2007-10-01; US20030527323P Applic. Date: 2003-12-05; US20040587787P Applic. Date: 2004-07-13; US20040614683P Applic. Date: 2004-09-30
Inventor: SIMPSON PETER C [US]; KAMATH APURV ULLAS [US]; LEACH JACOB S [US]; BRISTER MARK [US]; SWANSON VANCE [US]; HANSON CURTIS [US]; PRYOR JACK [US]; WIGHTLIN MATTHEW [US]; SAINT SEAN [US]; NOLTING JOHN [US]
Application No.: US20080199900A1 Published: 21/Aug/2008Title: Disposable Device For One Or More Introductions, Treatment And Sampling Of Biological Material From At Least One Of The Separation Phases Present Within The Device, Under Sterility Conditions and Constant Pressure
Applicant/Assignee: UNIVERSITA' DEGLI STUDI DI ROMA "LA SPIENZA"
Application No.: 11/659076 Filing Date: 07/Jul/2005
Abstract:A disposable device ( 1 ) for introduction, treatment and sampling of biological material from at last one of the separation phases under sterility and constant pressure conditions includes a sealed sterile test tube ( 2 ), having a first opening ( 4 ), or sampling opening, a second opening ( 7 ) or inlet opening, and a third opening ( 8 ), the first opening ( 4 ) providing the passage of a needle ( 5 ), coupling between the needle ( 5 ) and the first opening ( 4 ) being a sealing coupling by an elastic element ( 6 ) allowing translation in a substantially vertical direction and inclination of the needle ( 5 ). The second opening is sealed by a membrane ( 7 ) made of a material allowing the piercing by a syringe needle and closing back after the removal of the needle, the third opening ( 8 ) providing a sealing valve ( 8 ) balancing the pressure inside the test tube and environmental pressure.
Priority: IT2004RM00397 Applic. Date: 2004-08-04; WO2005IT00390 Applic. Date: 2005-07-07
Inventor: SIGNORE ALBERTO [IT]; ANNOVAZZI ALESSIO [IT]
Application No.: US20080200533A1 Published: 21/Aug/2008Title: Drug or Pharmaceutical Compounds and a Preparation Thereof
Applicant/Assignee:
Application No.: 11/994752 Filing Date: 29/Jun/2006
Abstract:The administration of pharmaceuticals of drugs which are having less solubility, lower bioavailability, lower bioabsorbability, less rate of absorption has become a big challenge in day to day life. Therefore an attempt has been made to prepare a complex modified form of the said pharmaceutical or drug such that the modified complex drugs or pharmaceuticals exhibits the enhanced properties of solubility, bioavailability, bioabsorbability and rate of absorption despite the increased complexity of the molecule. Surprisingly such modification was found to enhance retentivity of the active drug ingredient in the blood. Higher amounts of the active drug ingredient has shown lower toxicity.
Priority: IN2005CH00861 Applic. Date: 2005-07-04; WO2006IN00222 Applic. Date: 2006-06-29
Inventor: KRISHNAN RAMU [IN]
Application No.: US200802008038A1 Published: 21/Aug/2008Title: WEARABLE, PROGRAMMABLE AUTOMATED BLOOD TESTING SYSTEM
Applicant/Assignee:
Application No.: 11/469586 Filing Date: 01/Sep/2006
Abstract:The present invention is a programmable, automated device for measurement and analysis of blood analytes and blood parameters. The device components are preferably combined in a single housing and either programmed to initiate automatic, periodic blood sampling or initiate automatic blood sampling via operator input or in response to a predefined event or in response to a signal from another instrument. The device operates automatically to draw blood samples and analyze the drawn blood samples to obtain the desired blood readings.
Priority: US2005-287897 Applic. Date: 2005-11-28
Inventor: GOLDBERGER DANIEL [US]; SHREVE ERIC [US]; SIEBRECHT WAYNE [US]; PESACH BENNY [IL]; PESACH GIDI [IL]; BITTON GABBY [IL]; NAGAR RON [IL]; ARGAMAN DALIA [IL]; BELLOMO STEPHEN [IL]; LARSON ROBERT [US]; JOHNSON LARRY [US]; KLOMHAUS JILL [US]
Application No.: US20080213743A1 Published: 04/Sep/2008Title: Method for adjusting sedimentation rates
Applicant/Assignee:
Application No.: 12/071234 Filing Date: 19/Feb/2008
Abstract:One or more chemicals are added to a physiological fluid to alter the density and/or shape of cells in the fluid to provide a desired sedimentation rate of the cells. In a preferred embodiment, the chemical to be added is an anticoagulant, preferably ACD.
Priority: US20070901660P Applic. Date: 2007-02-16
Inventor: ELLSWORTH JAMES R [US]; KEVY SHERWIN [US]; JACOBSON MAY [US]
Application No.: US20080214978A1 Published: 04/Sep/2008Title: METHOD OF TREATING A BODILY FLUID
Applicant/Assignee: INTEGRATED SENSING SYSTEMS, INC
Application No.: 12/106642 Filing Date: 21/Apr/2008
Abstract:A method of treating a bodily fluid withdrawn and then returned to a living body. The method involves withdrawing the bodily fluid from the living body and causing the bodily fluid to flow through a treatment system, altering at least the density of the bodily fluid through the action of a second fluid as the bodily fluid flows through the treatment system, sensing at least the density and flow rate of the bodily fluid before the density thereof is altered by the second fluid, sensing at least the density and flow rate of the bodily fluid after the density thereof is altered by the second fluid, sensing at least the density and flow rate of the second fluid, controlling the density and/or flow rate of the second fluid based on the sensed densities and flow rates, and returning the bodily fluid to the living body.
Priority: US2005-160403 Applic. Date: 2005-06-22; US20040582976P Applic. Date: 2004-06-28
Inventor: SPARKS DOUGLAS RAY [US]; NAJAFI NADER [US]
Application No.: US20080215136A1 Published: 04/Sep/2008Title: DIFFERENTIAL DRUG RELEASE FROM A MEDICAL DEVICE
Applicant/Assignee:
Application No.: 11/953969 Filing Date: 11/Dec/2007
Abstract:The invention relates to a medical device, such as an intravascular stent, useful for delivering two or more therapeutic agents to a body tissue of a patient at different rates, and methods for making and using such medical device. The medical device includes a substrate and/or coating having a plurality of pores, dispersed in said pores are a plurality of a first and second therapeutic agents, wherein said first therapeutic agent is bonded to one or more molecule(s) of a first material and the second therapeutic agent bonded to one or more molecule(s) of a second material, such that when the medical device, is in use (e.g., implanted into a body lumen such as a blood vessel), bonded first therapeutic agent is released from the medical device at a rate that is slower than the rate at which the bonded second therapeutic agent is released from the medical device.
Priority: US20060877266P Applic. Date: 2006-12-26
Inventor: GREGORICH DANIEL J [US]; MEYER MIKE [US]
Application No.: US20080219998A1 Published: 11/Sep/2008Title: Anti-Thrombotic Agents
Applicant/Assignee:
Application No.: 10/486159 Filing Date: 08/May/2002
Abstract:The present invention embodies: methods
compounds, their pharmaceutically acceptable analogs, isomer, salts, hydrates, solvates and prodrug derivatives, and pharmaceutically acceptable compositions thereof that have particular biological properties
devices
diagnostic and other assays
and the uses of such methods, compounds, devices and assays. Common throughout these embodiments is specific selective reduction of intravascular thromboplastin antecedent activity, which results in a safe antithrombotic effect. A particularly prominent application or the invention relates to diagnosis and treatment of patients which have, or are at risk of, developing thrombosis, thrombotic injury, or vaso-occlusive diseases, such as myocardial infarction, stroke, restenosis after angioplasty, thrombotic diseases, etc. Another particularly prominent feature of the present invention is its high level of hemostatic safety at optimal efficacy. Also, the present invention is compatible for use in combination with other traditional therapeutic agent such as another antithrombotic, antiplatelet, thrombolytic, or anticoagulant agents.
Priority: US20010340294P Applic. Date: 2001-12-07; WO2002US14510 Applic. Date: 2002-05-08
Inventor: GRUBER ANDRAS [US]
Application No.: US20080220075A1 Published: 11/Sep/2008Title: Nanoparticulate compositions of angiogenesis inhibitors
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 12/076247 Filing Date: 14/Mar/2008
Abstract:Nanoparticulate compositions comprising at least one poorly soluble angiogenesis inhibitor and at least one surface stabilizer are described. The nanoparticulate compositions have an average particle size of less than about 2000 nm. The invention also describes methods of making and using such compositions.
Priority: US2003-392403 Applic. Date: 2003-03-20; US20020365540P Applic. Date: 2002-03-20; US20020366542P Applic. Date: 2002-03-25
Inventor: MERISKO-LIVERSIDGE ELAINE [US]; BOSCH H WILLIAM [US]; CARY GRETA G [US]; PRUITT JOHN [US]; RYDE TUULA [US]; JAIN RAJEEV [US]; WALTERS AMY [US]
Application No.: US20080226732A1 Published: 18/Sep/2008Title: NANOPARTICULATE COMPOSITIONS OF ANGIOGENESIS INHIBITORS
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 11/928289 Filing Date: 30/Oct/2007
Abstract:Nanoparticulate compositions comprising at least one poorly soluble angiogenesis inhibitor and at least one surface stabilizer are described. The nanoparticulate compositions have an average particle size of less than about 2000 nm. The invention also describes methods of making and using such compositions.
Priority: US2003-392403 Applic. Date: 2003-03-20; US20020366542P Applic. Date: 2002-03-25; US20020365540P Applic. Date: 2002-03-20
Inventor: MERISKO-LIVERSIDGE ELAINE [US]; BOSCH H WILLIAM [US]; CARY GRETA G [US]; PRUITT JOHN [US]; RYDE TUULA [US]; JAIN RAJEEV [US]; WALTERS AMY [US]
Application No.: US20080227083A1 Published: 18/Sep/2008Title: OPTICAL DETECTOR FOR ENZYME ACTIVATION
Applicant/Assignee:
Application No.: 12/127908 Filing Date: 28/May/2008
Abstract:Activation of an enzyme in a bodily fluid is detected based on the amount of cleavage of a substrate for the enzyme. The substrate is tagged with two fluorescent dyes-a donor and an acceptor. The tagged substrate is presented to the bodily fluid. A device emits energy at a first wavelength into the bodily fluid, and detects energy at second and third wavelengths emitted by the dyes in response to the energy at the first wavelength. Prior to enzymatic cleavage of the substrate, the acceptor emits energy at the third wavelength in response to energy at the second wavelength received through fluorescent resonant energy transfer (FRET) from the donor. After enzymatic cleavage of the substrate, the donor emits energy at the second wavelength. The device can determine the concentration of activated enzyme within the bodily fluid based on the relative intensities of energy, at the second and third wavelengths.
Priority: US2003-423112 Applic. Date: 2003-04-25
Inventor: SOYKAN ORHAN [US]; DONOVAN MAURA G [US]
Application No.: US20080233554A1 Published: 25/Sep/2008Title: COMPOSITION FOR PRESERVING PLATELETS AND METHOD OF USING THE SAME
Applicant/Assignee: BIOVEC, LLC
Application No.: 12/109784 Filing Date: 25/Apr/2008
Abstract:The present invention relates to compositions and methods for storing platelets to preserve the function and freshness of the platelets. More particularly, the present invention relates to the use of a preservative composition having an antiplatelet agent, an anticoagulant, and an oxygen carrier, for maintaining the freshness of platelets. Additionally, the composition may also contain an ultra-short acting broad spectrum anti-microbial agents. The preservative composition may be used to store platelets in a liquid state, a frozen state, or a freeze-dried state.
Priority: US2006-330132 Applic. Date: 2006-01-12; US20050643107P Applic. Date: 2005-01-12
Inventor: SEHGAL LAKSHMAN R [US]; MOUSA SHAKER [US]
Application No.: US20080241001A1 Published: 02/Oct/2008Title: Protease Inhibitor Sample Collection System
Applicant/Assignee: BECTON, DICKINSON AND COMPANY
Application No.: 11/937954 Filing Date: 09/Nov/2007
Abstract:A collection container and a method for collecting a biological sample, particularly whole blood, includes at least one stabilizing agent in an amount effective to stabilize and inhibit protein degradation and/or fragmentation. The stabilizing agent is able to stabilize proteases in the biological sample, particularly at the point of collection, by inhibiting protein degradation and/or fragmentation in the sample when the sample is stored. The stabilizing agent comprises or consists of one or more protease inhibitors.
Priority: US2003-436263 Applic. Date: 2003-05-13; US20020379399P Applic. Date: 2002-05-13
Inventor: HAYWOOD BRUCE [US]; DASTANE AJIT [US]; LIN FU-CHUNG [US]
Application No.: US20080241289A1 Published: 02/Oct/2008Title: PREPARATION AND UTILITY OF NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/035763 Filing Date: 22/Feb/2008
Abstract:Disclosed herein are non-nucleoside reverse transcriptase inhibitors having structural Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and the methods of their use thereof.
Priority: US20070891436P Applic. Date: 2007-02-23
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20080241349A1 Published: 02/Oct/2008Title: PROCESS FOR PREPARING A SUBSTRATE COATED WITH A BIOMOLECULE
Applicant/Assignee: ENSION, INC
Application No.: 12/061212 Filing Date: 02/Apr/2008
Abstract:Processes are provided for preparing a substrate coated with a biomolecule, comprising: a) providing a substrate
b) coating the substrate with a polysiloxane, typically by exposing the substrate to a reactive gas containing siloxane functional groups and to plasma energy to yield a plasma-deposited polysiloxane surface on the substrate
c) rendering the polysiloxane surface amino functional
and d) contacting the amino-functional polysiloxane surface with a biomolecule under conditions effective to attach the biomolecule to the substrate. The coated substrate may be a medical device that demonstrates an ability to maintain gas permeability when in contact with blood or blood components, compared to a substantially identical medical device that has not been coated with a biomolecule using this process.
Priority: US20070909553P Applic. Date: 2007-04-02
Inventor: CAHALAN PATRICK [US]; CAHALAN LINDA [US]; JOHNSON GREG [US]; GARTNER MARK [US]
Application No.: US20080248107A1 Published: 09/Oct/2008Title: Controlled Release Formulation
Applicant/Assignee: RUBICON RESEARCH PVT. LTD
Application No.: 12/064687 Filing Date: 24/Aug/2006
Abstract:The present invention provides a controlled release formulation comprising an therapeutically effective amount of pharmacologically active substance having high water solubility, at least one non-polymeric release retardant, and at least one pH independent non-swelling release retarding polymer. The said dosage form provides controlled release of the active agent with reduced initial burst release.
Priority: IN2005MU01001 Applic. Date: 2005-08-24; WO2006IN00309 Applic. Date: 2006-08-24
Inventor: PILGAONKAR PRATIBHA S [IN]; RUSTOMJEE MAHARUKH T [IN]; GANDHI ANIKUMAR S [IN]; KELKAR ATUL A [IN]; BAGDE PRADNYA [IN]
Application No.: US20080254036A1 Published: 16/Oct/2008Title: COMBINATION ANTICOAGULANT THERAPY WITH A COMPOUND THAT ACTS AS A FACTOR XA INHIBITOR
Applicant/Assignee: MILLENNIUM PHARMACEUTICALS, INC
Application No.: 12/101644 Filing Date: 11/Apr/2008
Abstract:The present invention is directed to methods of using combination therapies containing [2-({4-[(dimethylamino)iminomethyl]phenyl}carbonylamino)-5-methoxyphenyl]-N-(5-chloro(2-pyridyl))carboxamide for the treatment of thrombotic disease(s) and pharmaceutical compositions thereof.
Priority: US20070911852P Applic. Date: 2007-04-13
Inventor: SINHA UMA [US]; HOLLENBACH STANLEY J [US]; ANDRE PATRICK [US]
Application No.: US20080254146A1 Published: 16/Oct/2008Title: METHOD OF PROVIDING HEMOSTASIS IN ANTI-COAGULATED BLOOD
Applicant/Assignee: Z-MEDICA CORPORATION
Application No.: 12/101336 Filing Date: 11/Apr/2008
Abstract:A method of clotting blood includes the step of administering a therapeutically effective amount of a composition comprising zeolite as the active ingredient to a wound from which the blood emanates. A method of arresting blood flowing from a wound includes the steps of providing a patient being inflicted with a bleeding wound and administering a therapeutically effective amount of a composition comprising zeolite as the active ingredient to the bleeding wound. A method of facilitating the formation of blood clots includes the step of contacting blood with a negatively charged surface wherein upon contacting the blood with the negatively charged surface a clotting mechanism is initiated. In any of the foregoing methods, the blood has a compromised ability to form clots. The blood may be from a person diagnosed with hemophilia or von Willebrand disease.
Priority: US20070923416P Applic. Date: 2007-04-13
Inventor: HUEY RAYMOND J [US]; BASADONNA GIACOMO [US]
Application No.: US20080254147A1 Published: 16/Oct/2008Title: METHOD OF PROVIDING HEMOSTASIS IN ANTI-COAGULATED BLOOD
Applicant/Assignee: Z-MEDICA CORPORATION
Application No.: 12/101346 Filing Date: 11/Apr/2008
Abstract:In a method of clotting blood in which the blood exhibits a reduced tendency to clot and may be from a person undergoing an anticoagulant therapy or having type A or B hemophilia or von Willebrand disease, a therapeutically effective amount of a composition comprising clay as the active ingredient is administered to a wound from which the blood emanates. Upon contacting the blood, this clay, which may be kaolin, bentonite, or any type of layered clay, causes the blood to clot. In a method of arresting blood flowing from a wound, a therapeutically effective amount of a composition comprising clay as the active ingredient is administered to the bleeding wound. In this method, the blood has a reduced tendency to clot and may be from a person undergoing an anticoagulant therapy or having at least one of hemophilia A or B or von Willebrand disease.
Priority: US2008-101336 Applic. Date: 2008-04-11; US20070923416P Applic. Date: 2007-04-13
Inventor: HUEY RAYMOND J [US]; BASADONNA GIACOMO [US]
Application No.: US20080255352A1 Published: 16/Oct/2008Title: Cyclic amide derivative, and its production and use
Applicant/Assignee: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Application No.: 12/157574 Filing Date: 11/Jun/2008
Abstract:The present invention provides a cyclic amide derivative useful as a drug for treating thrombosis, which is represented by the formula (I): wherein R<1 >represents an optionally substituted cyclic hydrocarbon group or an optionally substituted heterocyclic group, W represents a bond or an optionally substituted divalent chain hydrocarbon group, a represents 0, 1, or 2, X<1 >represents an optionally substituted lower alkylene or an optionally substituted lower alkenylene, Y<1 >represents -C(O)-, -S(O)- or -S(O)2-, A represents a piperazine ring which may be further substituted or a piperidine ring which may be further substituted, X<2 >represents a bond or an optionally substituted lower alkylene, Y<2 >represents -C(O)-, -S(O)-, -S(O)2- or -C(-NR<7>)-, X<3 >represents an optionally substituted C1-4 alkylene or an optionally substituted C2-4 alkenylene, Z<3 >represents -N(R<4>)-, -O- or a bond, Z<1 >represents -C(R<2>)(R<2'>)-, -N(R<2>)-, etc., and Z<2 >represents -C(R<3>)(R<3'>)-, -N(R<3>)-, etc., or a salt thereof.
Priority: JP20040152000 Applic. Date: 2004-05-21; US2006-596089 Applic. Date: 2006-11-09; WO2005JP09711 Applic. Date: 2005-05-20
Inventor: KUBO KEIJI [JP]; IMAEDA YASUHIRO [JP]
Application No.: US20080260710A1 Published: 23/Oct/2008Title: Method for Suppressing Surgical Site Infection and Column to be Used for the Method
Applicant/Assignee: ASAHI KASEI MEDICAL CO., LTD
Application No.: 11/572405 Filing Date: 23/Jun/2005
Abstract:An object of the present invention is to provide a method for suppressing surgical site infections (SSI) that have occurred at extremely high incidence rates at the time of surgical operations and particularly surgical operations on digestive system organs, and to provide a column to be used for the method. According to the present invention, a method is provided for suppressing surgical site infections, which comprises the steps of: (a) administering a chemotherapeutic drug for treating and/or preventing a surgical site infection
and (b) collecting blood from a surgical subject and removing leukocytes that comprise neutrophils from the blood during or within 24 hours after surgical operation, and then returning the blood from which the leukocytes have been removed to the surgical subject. The present invention also provides a column for blood circulation which is filled with a carrier having affinity for leukocytes comprising neutrophils, which is used for suppressing a surgical site infection during or within 24 hours after surgical operation on a digestive system organ.
Priority: JP20040213998 Applic. Date: 2004-07-22; JP20050009201 Applic. Date: 2005-01-17; WO2005JP11501 Applic. Date: 2005-06-23
Inventor: KUSUNOKI MASATO [JP]; MIKI CHIKAO [JP]; YOSHIYAMA SHIGEYUKI [JP]
Application No.: US20080261861A1 Published: 23/Oct/2008Title: 2-Micron Family Plasmid and Use Thereof
Applicant/Assignee: DELTA BIOTECHNOLOGY LIMITED
Application No.: 10/584486 Filing Date: 23/Dec/2004
Abstract:The present invention provides a 2 mum-family plasmid comprising a polynucleotide sequence insertion, deletion and/or substitution between the first base after the last functional codon of at least one of either a REP2 gene or an FLP gene and the last base before the FRT site in an inverted repeat adjacent to said gene.
Priority: GB20030029722 Applic. Date: 2003-12-23; WO2004GB05435 Applic. Date: 2004-12-23
Inventor: SLEEP DARRELL [GB]; FINNIS CHRISTOPHER JOHN ARTHUR [GB]
Application No.: US20080268021A1 Published: 30/Oct/2008Title: Adhesive bioerodible ocular drug delivery system
Applicant/Assignee: QLT USA, INC
Application No.: 12/215101 Filing Date: 24/Jun/2008
Abstract:The present invention provides bioerodible, water-soluble pharmaceutical carriers for ocular (e.g., transconjunctival or transcorneal) delivery of pharmaceuticals for either systemic or local therapy.
Priority: US2003-706603 Applic. Date: 2003-11-12; US20020425508P Applic. Date: 2002-11-12
Inventor: WARREN STEPHEN L [US]; OSBORNE DAVID W [US]; HOLL RICHARD [US]
Application No.: US20080268483A1 Published: 30/Oct/2008Title: Methods for a Global Assay of Coagulation and Fibrinolysis
Applicant/Assignee: THE REGENTS OF THE UNIVERSITY OF COLORADO
Application No.: 11/575853 Filing Date: 22/Sep/2005
Abstract:The present disclosure concerns methods of analyzing both clot formation and fibrinolysis in a sample, preferably simultaneously. In certain embodiments, the methods may comprise adding a small amount of at least one activator of coagulation and at least one activator of fibrinolysis to a sample and analyzing the sample for kinetic parameters related to clot formation and fibrinolysis. In another embodiment, the methods may comprise analyzing a sample from a subject for clot formation and fibrinolysis and detecting or diagnosing a disease or condition and/or applying information obtained from analyzing clot formation and fibrinolysis to determine a treatment for a medical condition of the subject.
Priority: US20040612580P Applic. Date: 2004-09-22; WO2005US33999 Applic. Date: 2005-09-22
Inventor: GOLDENBERG NEIL A [US]; MANCO-JOHNSON MARILYN J [US]; JACOBSON LINDA [US]; HATHAWAY WILLIAM E [US]
Application No.: US20080269176A1 Published: 30/Oct/2008Title: New Salts
Applicant/Assignee: ASTRAZENECA AB
Application No.: 11/839842 Filing Date: 16/Aug/2007
Abstract:There is provided pharmaceutically-acceptable acid addition salts of compounds of formula (I), wherein R<1 >represents C1-2 alkyl substituted by one or more fluoro substituents
R<2 >represents C1-2 alkyl
and n represents 0, 1 or 2, which salts are useful as prodrugs of competitive inhibitors of trypsin-like proteases, such as thrombin, and thus, in particular, in the treatment of conditions where inhibition of thrombin is required.
Priority: SE20020001661 Applic. Date: 2002-05-31; US2005-516422 Applic. Date: 2005-05-20; WO2003SE00859 Applic. Date: 2003-05-27
Inventor: AHLQVIST MATTI [SE]; BOHLIN MARTIN [SE]; INGHARDT TORD [SE]; LUNDBLAD ANITA [SE]; SIGFRIDSSON CARL-GUSTAF [SE]
Application No.: US20080269762A1 Published: 30/Oct/2008Title: METHOD AND DEVICE FOR REPAIR OF CARTILAGE DEFECTS
Applicant/Assignee: BIOMET MANUFACTURING CORP
Application No.: 11/740014 Filing Date: 25/Apr/2007
Abstract:Methods for repairing a cartilage defect in a subject, such methods comprising placing a tissue specimen into a container, centrifuging the container to separate the specimen into at least three fractions, drawing a selected fraction from the container, processing the fraction into a therapeutic composition, and treating the cartilage defect with the therapeutic composition.
Priority:
Inventor: SIMON BRUCE [US]; WOODELL-MAY JENNIFER E [US]
Application No.: US20080274477A1 Published: 06/Nov/2008Title: Forms of Factor Xiia
Applicant/Assignee:
Application No.: 11/795074 Filing Date: 10/Jan/2006
Abstract:A 53 Kd novel form of factor XIIa and related products, including nucleic acid molecules, monoclonal and polyclonal antibodies and hybridoma cell lines. Also assays for a 53 Kd form of factor XIIa and uses of said assays in diagnostic and prognostic methods, for example in the prediction of survival following myocardial infarction.
Priority: GB20050000487 Applic. Date: 2005-01-11; WO2006GB00072 Applic. Date: 2006-01-10
Inventor: PRITCHARD DAVID JOHN [GB]
Application No.: US20080286290A1 Published: 20/Nov/2008Title: Anti-Cd14 Antibody Fusion Protein
Applicant/Assignee:
Application No.: 11/791888 Filing Date: 05/Jun/2006
Abstract:A protein comprising (I) an anti-CD14 antibody or its active fragment, or a derivative thereof and (II) an inhibitor for a protease, or its active fragment, or a derivative thereof is provided.
Priority: JP20050164901 Applic. Date: 2005-06-03; WO2006JP11255 Applic. Date: 2006-06-05
Inventor: FURUSAKO SHOJI [JP]; NAKAYAMA KAZAYUKI [JP]; HOSAKA YOSHITAKA [JP]; KAWAHARA TETSUSHI [JP]; NAKAMURA MASAKI [JP]; TAKEUCHI TAKASHI [JP]
Application No.: US20080286327A1 Published: 20/Nov/2008Title: THOMBOLYSIS AND CHRONIC ANTICOAGULATION THERAPY
Applicant/Assignee:
Application No.: 11/949752 Filing Date: 03/Dec/2007
Abstract:Method and systems of treating a patient with at least one of a myocardial infarction, a stroke, and a pulmonary embolism include providing a stimulator coupled to at least one electrode and a catheter, configuring one or more stimulation parameters to treat at least one of a myocardial infarction, a stroke, and a pulmonary embolism, programming the stimulator with the one or more stimulation parameters, delivering with the stimulator via the catheter at least one drug to at least one tissue in accordance with the one or more stimulation parameters, and limiting perfusion of the at least one tissue by delivering electrical stimulation with the stimulator via the at least one electrode to the at least one tissue.
Priority: US2002-285803 Applic. Date: 2002-11-01; US20010340076P Applic. Date: 2001-11-01
Inventor: WHITEHURST TODD K [US]; MCCLURE KELLY H [US]; THACKER JAMES R [US]
Application No.: US20080286329A1 Published: 20/Nov/2008Title: Methods and Apparatus for Manufacturing Plasma Based Plastics and Bioplastics Produced Therefrom
Applicant/Assignee: CARNEGIE MELLON UNIVERSITY ALLEGHENY-SINGER RESEARCH INSTITUTE CARMELL, LLC
Application No.: 12/104728 Filing Date: 17/Apr/2008
Abstract:Blood-derived plastic articles prepared from compositions including blood and, in some embodiments, at least one crosslinking agent and/or at least one biological response modifier, that can be useful for biological applications such as wound repair and tissue grafts
methods of making and using the same
methods for assessing the concentration of a biological response modifier in an article
and systems for preparing blood-derived plastic articles are provided.
Priority: US2007-873751 Applic. Date: 2007-10-17; US2006-495115 Applic. Date: 2006-07-28; US2003-391458 Applic. Date: 2003-03-18; US20060852368P Applic. Date: 2006-10-17; US20070961580P Applic. Date: 2007-07-23; US20050703206P Applic. Date: 2005-07-28; US20020365451P Applic. Date: 2002-03-18
Inventor: CAMPBELL PHIL G [US]; BURGESS JAMES E [US]; WEISS LEE E [US]; SMITH JASON [US]
Application No.: US20080287829A1 Published: 20/Nov/2008Title: COLLECTION MEANS AND A METHOD FOR COLLECTING CORD BLOOD
Applicant/Assignee:
Application No.: 12/062500 Filing Date: 03/Apr/2008
Abstract:The invention provided herein comprises a kit, where the kit includes at least one collecting receptacle for collecting cord blood, and a pre-measured non-liquid anticoagulant which is optionally pre-loaded into the receptacle. The anticoagulant is preferably selected from the group consisting of heparin or heparin type additives, citrates, EDTA (ethylenediaminetetraacetic acid), and oxalates and any other anticoagulant that can be used to decrease the clotting ability of the blood. The invention provided herein also comprises a method for collecting cord blood, where the method comprises collecting a desired amount of cord blood from the umbilical cord using a collection receptacle of the invention, wherein the collection receptacle is pre-loaded with a pre-measured amount of non-liquid anticoagulant.
Priority: US2005-186415 Applic. Date: 2005-07-20; US20040590386P Applic. Date: 2004-07-20
Inventor: MOORE THOMAS E [US]; MAPOTHER BETH [US]
Application No.: US20080292707A1 Published: 27/Nov/2008Title: Pharmaceutical Compositions of Adsorbates of Amorphous Drug
Applicant/Assignee: PFIZER INC
Application No.: 12/180769 Filing Date: 28/Jul/2008
Abstract:Pharmaceutical compositions comprise a low-solubility drug adsorbed onto a high surface area substrate to form an adsorbate. The compositions in some embodiments include a concentration-enhancing polymer.
Priority: US2002-173987 Applic. Date: 2002-06-17; US20010300260P Applic. Date: 2001-06-22
Inventor: BABCOCK WALTER C [US]; FRIESEN DWAYNE T [US]; SHANKER RAVI M [US]; SMITHEY DANIEL T [US]; TADDAY RALPH [US]
Application No.: US20080293628A1 Published: 27/Nov/2008Title: Methods and Compositions for the Inhibition of Thrombus Formation
Applicant/Assignee:
Application No.: 11/579291 Filing Date: 27/Apr/2005
Abstract:The present invention is directed to anti-platelet peptides that may be used in various methods for the treatment or prophylaxis of thrombosis. More specifically, the specification describes methods and compositions for making and using compositions GPIbalpha fragments as anti-platelet agents. The present invention is also directed to peptides that inhibit intracellular function of 14-3-3.
Priority: US20040568042P Applic. Date: 2004-05-04; WO2005US14528 Applic. Date: 2005-04-27
Inventor: DAI KESHENG [US]; DU XIAOPING [US]
Application No.: US20080299186A1 Published: 04/Dec/2008Title: COATINGS FOR APPLYING SUBSTANCES ONTO SUBSTRATE CARRIER
Applicant/Assignee: SCHERING-PLOUGH HEALTHCARE PRODUCTS, INC
Application No.: 12/130225 Filing Date: 30/May/2008
Abstract:Compositions of matter containing an active agent, and methods of manufacturing thereof, wherein the method comprises the step of coating a substrate with a coating composition comprising the active agent formulated for immediate release, wherein the coating composition does not contain an appreciable amount of cellulosic materials and preferably comprises polyvinyl alcohol or a polyvinyl alcohol derived copolymer.
Priority: US20070941577P Applic. Date: 2007-06-01
Inventor: FRITZ GLENN E [US]; REO JOSEPH P [US]; KABIR MOHAMMED A [US]
Application No.: US20080299587A1 Published: 04/Dec/2008Title: METHODS OF MEASURING INHIBITION OF PLATELET AGGREGATION BY THROMBIN RECEPTOR ANTAGONISTS
Applicant/Assignee:
Application No.: 12/114498 Filing Date: 02/May/2008
Abstract:A method is provided for measuring inhibition of platelet aggregation by a thrombin receptor antagonist. First, a blood sample is obtained from a patient treated with a thrombin receptor antagonist. The blood sample is mixed in combination with particles including an immobilized GPIIb/IIIa receptor ligand and a thrombin receptor activator. The combination is then incubated under conditions suitable for agglutinating the particles, and platelet-mediated agglutination is assessed in the mixture. The absence of agglutination indicates that the patient has reduced ability to form platelet thrombi in response to the thrombin receptor antagonist treatment. Also provided is a kit for measuring inhibition of platelet aggregation by a thrombin receptor antagonist that includes a GPIIb/IIIa receptor ligand immobilized on a particle, a thrombin receptor activator, an anticoagulant, and a buffer to maintain the anticoagulated blood in a condition suitable for platelet aggregation.
Priority: US20070915820P Applic. Date: 2007-05-03
Inventor: DURBIN DENNIS [US]
Application No.: US20080300489A1 Published: 04/Dec/2008Title: Cable and connector system for an ultrasound probe
Applicant/Assignee:
Application No.: 11/895613 Filing Date: 24/Aug/2007
Abstract:A finger-mounted ultrasound probe assembly having an ultrasound probe, adapted to be mounted on a finger and a multi-conductor cable, attached to the ultrasound probe. In addition, a forearm unit is connected to the multi-conductor cable and includes a physical connector to bind the forearm unit to a user's forearm. Also, the ultrasound probe and the forearm unit are adapted to cooperatively engage so that the ultrasound probe may be engaged to and retained by the forearm unit, to stow the ultrasound probe when not in immediate use.
Priority: US20070923323P Applic. Date: 2007-04-13
Inventor: SCHUTZ RONALD W [US]; CORBETT III SCOTT S [US]; BATES KENNETH N [US]; MCDONOUGH WILLIAM [US]; KRAUSE ALBERT H [US]
Application No.: US20080305160A1 Published: 11/Dec/2008Title: Oral Medicament For The Modified Release Of At Least One Active Principle, In Multimicrocapsule Form
Applicant/Assignee: FLAMEL TECHNOLOGIES
Application No.: 11/791466 Filing Date: 02/Nov/2005
Abstract:The field of the invention is that of oral medicaments or pharmaceutical compositions, in particular of the type including one or more active principles. The aim of the invention is to provide an improved oral medicament to be administered in one or several daily doses and enabling the modified release of active principles (in particular of one active principle), whereby the prophylactic and therapeutic effectiveness of said medicament is improved. This aim is achieved by the oral multimicrocapsule galenic form according to the invention, in which the active principle release is controlled by a dual release trigger mechanism: "time-dependent trigger" and "pH-dependent trigger". Said medicament includes microcapsules providing the modified release of the active principle, each comprising a core containing
Priority: FR20040052748 Applic. Date: 2004-11-24; WO2005FR50922 Applic. Date: 2005-11-02
Inventor: GUIMBERTEAU FLORENCE [FR]; CASTAN CATHERINE [FR]; MEYRUEIX REMI [FR]; SOULA GERARD [FR]
Application No.: US20080312576A1 Published: 18/Dec/2008Title: PLUNGER-LESS SYRINGE FOR CONTROLLING BLOOD FLOW
Applicant/Assignee:
Application No.: 12/140181 Filing Date: 16/Jun/2008
Abstract:A plunger-less syringe, method of manufacture and system of use is disclosed wherein the syringe includes a barrel that has an interior receptacle for receiving a quantity of blood. The syringe has at least one filter that controls fluid flow within the syringe. The syringe may be fabricated from a material that prevents diffusion of the gas from the blood. Different syringes may comprise different fluid flow characteristics. In addition, the components of the syringe may include indicia so a syringe having particular characteristics can be selected for patients with different blood pressure.
Priority: US20070944315P Applic. Date: 2007-06-15
Inventor: MCKINNON ROBERT J [US]; BICKLEY JAMES DALE [US]
Application No.: US20080318259A1 Published: 25/Dec/2008Title: Hematocrit and Analyte Concentration Determination
Applicant/Assignee: ZAFENA AKTIEBOLAG
Application No.: 10/581094 Filing Date: 02/Dec/2004
Abstract:A method to determine an analyte concentration of an anticoagulated plasma by performing at least two different measurements on a mixture of a blood sample corresponding to said anticoagulant plasma and of liquid reagent is described. The method comprises a) mixing a volume of said blood sample with a five-fold, or more, volume of said liquid reagent, b) performing said at least two measurements on said mixture, at least one of which correlates with the hematocrit of said blood sample and at least one of which correlates with said analyte concentration, and c) computing the results from the measurements when the volumes in a) are precise and accurate or when the hematocrit of said blood sample in b) is known to determine said analyte concentration of said anticoagulated plasma. In addition, a measurement and determination device for performing measurements on blood, anticoagulated blood and/or anticoagulated plasma samples, and an equipment kit are described.
Priority: SE20030003249 Applic. Date: 2003-12-02; WO2004SE01798 Applic. Date: 2004-12-02
Inventor: RANBY MATS [SE]
Application No.: US20090000630A1 Published: 01/Jan/2009Title: Instant Face-Lifter
Applicant/Assignee:
Application No.: 11/986714 Filing Date: 26/Nov/2007
Abstract:Following are six improvements on the prior art entitled "Instant Face-Lifter". "Intra-scalp TV/Radio/Stereo-Music-Reproducing Device Face-Lifter": uses an intra-scalp silicone Face-Lifter as stand for an implanted TV set and/or AM-FM Radio and/or an Open Platform Stereo Music device (MP3, MP4 Ipod(R), Walkman(R), WMA(R)). "Intra-scalp GPS-Face-Lifter": a Face-Lifter as a stand for a GPS device. "Intra-scalp Heart Pace-Maker-Face-Lifter": a Face-Lifter as a stand for a heart pace-maker device. "Intra-scalp Artificial Hair Anchoring Base Face-Lifter": a Face-Lifter as an anchoring base for permanently implanting small bundles of artificial hair on balding people. "Intra-scalp Bullet-Proof Head-Armor Face-Lifter": a Face-Lifter as bullet-proof head armor. "Intra-scalp Orgasm-inducer Face-Lifter": a Face-Lifter as a stand for an orgasm-inducing electric device.
Priority: US20070905057P Applic. Date: 2007-03-05; US20070904996P Applic. Date: 2007-03-05; US20070995258P Applic. Date: 2007-09-25
Inventor: ARAY RICARDO ALFREDO FUENMAYOR [VE]
Application No.: US20090004281A1 Published: 01/Jan/2009Title: MULTIPARTICULATE OSMOTIC DELIVERY SYSTEM
Applicant/Assignee: BIOVAIL LABORATORIES INTERNATIONAL S.R.L
Application No.: 11/768764 Filing Date: 26/Jun/2007
Abstract:The present invention relates to a multiparticulate osmotic delivery system. The system is a modified release composition suitable for oral administration. The composition includes a core that includes at least one drug in combination with at least one pharmaceutically acceptable excipient. The composition further includes an osmotic subcoat surrounding the core, and a modified release overcoat surrounding the osmotic subcoated core.
Priority:
Inventor: NGHIEM TIEN [IE]; JACKSON GRAHAM [IE]
Application No.: US20090010886A1 Published: 08/Jan/2009Title: Method for the Treatment of Myeloproliferative Diseases Using(+)-2-[1-(3-Ethoxy-4-Methoxyphenyl)-2- Methylsulfonylethyl]-4- Acetylaminoisoindoline-1,3- Dione
Applicant/Assignee: CELGENE CORPORATION
Application No.: 11/579355 Filing Date: 22/Sep/2008
Abstract:Methods of treating, preventing and/or managing a myeloproliferative disease are disclosed. Specific methods encompass 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 the transplantation of blood or cells. Particular second active agent is capable of suppressing the overproduction of hematopoietic stem cells or ameliorating one or more of the symptoms of MPD. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in methods of the invention are also disclosed.
Priority: WO2004US14001 Applic. Date: 2004-05-05
Inventor: ZELDIS JEROME B [US]
Application No.: US20090011024A1 Published: 08/Jan/2009Title: Pharmaceutical compositions of dispersions of amorphous drugs mixed with polymers
Applicant/Assignee: PFIZER INC
Application No.: 12/217700 Filing Date: 08/Jul/2008
Abstract:A pharmaceutical composition comprises a dispersion comprising a low-solubility drug and a matrix combined with a concentration-enhancing polymer. At least a major portion of the drug is amorphous in the dispersion. The compositions improve the stability of the drug in the dispersion, and/or the concentration of drug in a use environment.
Priority: US2002-175640 Applic. Date: 2002-06-19; US20010300261P Applic. Date: 2001-06-22
Inventor: BABCOCK WALTER C [US]; CURATOLO WILLIAM J [US]; FRIESEN DWAYNE T [US]; KETNER RODNEY J [US]; LO JULIAN B [US]; NIGHTINGALE JAMES A S [US]; SHANKER RAVI M [US]; WEST JAMES B [US]
Application No.: US20090011451A1 Published: 08/Jan/2009Title: MICROFLUIDIC DEVICE AND LEUCOCYTE ANTIGEN MEDIATED MICROFLUIDIC ASSAY
Applicant/Assignee:
Application No.: 11/568832 Filing Date: 13/May/2005
Abstract:The present invention relates to an leucocyte antigen mediated microfluidic assay and a microfluidic device for analyzing a subjects' body fluids containing leucocytes to determine if the subject has been previously exposed to a predetermined antigen.
Priority: US20040570543P Applic. Date: 2004-05-13; WO2005US16974 Applic. Date: 2005-05-13
Inventor: RODRIGUEZ RODOLFO R [US]; DARR DOUGLAS J [US]
Application No.: US20090012426A1 Published: 08/Jan/2009Title: Intravascular Line and Port Cleaning Methods, Methods of Administering an Agent Intravascularly, Methods of Obtaining/Testing Blood, and Devices for Performing Such Methods
Applicant/Assignee: HYPROTEK, INC
Application No.: 12/211723 Filing Date: 16/Sep/2008
Abstract:An intravascular port access device includes a first component having a chamber configured to attach reversibly to an intravenous line port. A second component reversibly attaches to the first component and contains a disinfecting agent and an applicator material. The second component is configured to be reversibly received over external surfaces of the intravenous line port. A method of cleansing an intravenous line port includes providing a port cleaning device having a first component with a chamber containing a first cleaning agent. A second component includes a second cleaning agent. A third component has a microbiocidal agent and is reversibly attached to the first component. The second component is removed from the device, the external surfaces of the port are contacted with the second cleaning agent, the first cleaning agent is ejected from the chamber into the port, and the third component is used to cap the port.
Priority: US2007-745843 Applic. Date: 2007-05-08; US20060747606P Applic. Date: 2006-05-18; US20060842194P Applic. Date: 2006-08-31; US20070895621P Applic. Date: 2007-03-19
Inventor: TENNICAN PATRICK O [US]
Application No.: US20090012606A1 Published: 08/Jan/2009Title: BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS
Applicant/Assignee: ADVANCED CARDIOVASCULAR SYSTEMS, INC
Application No.: 12/207419 Filing Date: 09/Sep/2008
Abstract:This disclosure provides a method device and a method of forming the medical device. The medical device comprises a coating comprising a polymer. The polymer comprises at least two different blocks, at least one L1 block with the formula and at least one L2 block with the formula Medical devices comprising these polymers, mixtures of these polymers with therapeutic agents, and methods of making these polymers and mixtures are within the scope of this disclosure.
Priority: US2003-741214 Applic. Date: 2003-12-19
Inventor: PACETTI STEPHEN D [US]
Application No.: US20090022706A1 Published: 22/Jan/2009Title: SUBSTITUTED CYCLOHEXENES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/176163 Filing Date: 18/Jul/2008
Abstract:Disclosed herein are substituted cyclohexene TLR4 signaling pathway modulators of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20070951067P Applic. Date: 2007-07-20
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]; ZHANG CHENGZHI [US]
Application No.: US20090028873A1 Published: 29/Jan/2009Title: SUBSTITUTED CYCLOHEXANOLS
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/180421 Filing Date: 25/Jul/2008
Abstract:Disclosed herein are substituted cyclohexanol opioid receptor modulators and/or neurotransmitter reuptake modulators of Formula I or Formula II, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20070952292P Applic. Date: 2007-07-27
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090028948A1 Published: 29/Jan/2009Title: NANOPARTICLE COMPOSITION AND METHODS OF SYNTHESIS THEREOF
Applicant/Assignee: ICEUTICA PTY LTD
Application No.: 11/813116 Filing Date: 30/Dec/2005
Abstract:The present invention relates to improved therapeutically active nanocomposite microstructure compositions, including nanoparticle compositions and nanoparticle preparations. Preferred embodiments include nanoparticle compositions comprising nanoparticles of a therapeutically active agent dispersed in a carrier matrix. The invention also relates to a method for preparing said compositions and preparations using solid-state mechanochemical synthesis. Further, it relates to therapeutic products produced using said compositions and to methods of treatment using the compositions.
Priority: AU20040907377 Applic. Date: 2004-12-31; WO2005AU01977 Applic. Date: 2005-12-30
Inventor: PAYNE TREVOR [AU]; MEISER FELIX [AU]; POSTMA ALMAR [AU]; CAMMARANO RAFFAELE [AU]; WILLIAMS JAMES [AU]; MCCORMICK PAUL [AU]; DODD AARON [AU]; CARUSO FRANK [AU]
Application No.: US20090029342A1 Published: 29/Jan/2009Title: Medium and method for preserving platelets, red blood cells, and other non-nucleus cells and platelets-containing composition
Applicant/Assignee:
Application No.: 12/232482 Filing Date: 18/Sep/2008
Abstract:The present invention provides a platelet-containing composition prepared by contacting platelets with a medium for preserving. The medium comprises anticoagulant, cryoprecipitate and thrombin. The present invention also provides a method for long-term preservation of platelets, comprising the steps of: (a) adding an anticoagulant, cryoprecipitate, thrombin in normal saline
(b) adding a platelet-containing medium into the solution formed in step (a)
and (c) lyophilizing the platelet-containing solution formed in step (b). Moreover, the present invention yet provides a medium for preserving non-nucleus cells.
Priority: TW20040119184 Applic. Date: 2004-06-29; US2005-157838 Applic. Date: 2005-06-22
Inventor: SU CHENG YAO [TW]; LIN CHENG CHIH [TW]
Application No.: US20090029829A1 Published: 29/Jan/2009Title: NOSE TO BACK NECK AND EYE MUSCLES EXERCISE
Applicant/Assignee:
Application No.: 11/828458 Filing Date: 26/Jul/2007
Abstract:A nose to back neck and eye muscles exercise for improved facial enhancement, resulting in a more youthful appearance because of reduced or eliminated wrinkling of the face, is one representation of this invention. This exercise affects all of the facial muscle area beginning at the nose and going upward, ending at the back of the neck area. Notable improvement results in a tightened, smaller slenderized nose and reduced or eliminated wrinkling around facial eye area and forehead. Not only is a more youthful appearance achieved, but eyesight (vision) is greatly improved from strengthened supportive facial muscles surrounding eyes and independently strengthened muscles of the eyes as a result of this exercise. It is not possible to receive one natural benefit of the muscles exercise of this present invention of reduced wrinkling and a more youthful appearance without receiving its naturally intertwined second benefit of improved eyesight, and vice versa.
Priority:
Inventor: FERRARA YOLANDA CARMEN [US]
Application No.: US20090030071A1 Published: 29/Jan/2009Title: Treatment of Cardiovascular Disease in Mexican Americans Using Nebivolol
Applicant/Assignee:
Application No.: 12/173125 Filing Date: 15/Jul/2008
Abstract:Nebivolol has been shown to be beneficial in the treatment of cardiovascular diseases such as, but not limited to, hypertension, congestive heart failure, arterial stiffness and endothelial dysfunction. The present invention relates to methods for treating and/or preventing cardiovascular disorders in persons of Hispanic descent, particularly Mexican Americans, using compositions comprising nebivolol.
Priority: US20070952015P Applic. Date: 2007-07-26
Inventor: SHAW ANDREW A [US]; MASON R PRESTON [US]; RIGGS BETTY [US]
Application No.: US20090036764A1 Published: 05/Feb/2009Title: FLUID INJECTION AND SAFETY SYSTEM
Applicant/Assignee: OPTISCAN BIOMEDICAL CORPORATION
Application No.: 12/123422 Filing Date: 19/May/2008
Abstract:Various medical systems and methods are described, including a medical monitoring system. The medical monitoring system can have a fluid system configured to receive bodily fluid and optically analyze said fluid to determine analyte concentration. The fluid system can have a removable portion. The removable portion can have an opening with a port. The system can also have a container configured to contain anticoagulant. The container can have a portion configured to mate with the port of the removable portion. The container can be further configured to not fit into a conventional luer fitting. An anti-coagulant insertion apparatus is also described. The apparatus can have a syringe, a dock with a port, and an adapter configured to connect the syringe to the port. The dock can also have a tab configured to move with the port.
Priority: US20070939023P Applic. Date: 2007-05-18; US20070979374P Applic. Date: 2007-10-11
Inventor: RIVAS GIL [US]; BUTLER MICHAEL [US]; CHIOU JEFFREY T [US]; LIM EUGENE [US]
Application No.: US20090036841A1 Published: 05/Feb/2009Title: COATINGS FOR BLOOD AND BONE MARROW-CONTACTING DEVICES
Applicant/Assignee:
Application No.: 12/184869 Filing Date: 01/Aug/2008
Abstract:Medical devices having an anticoagulant coating are described. The devices may be needles, syringes and blood processing devices. The anticoagulant coating can be any of heparin, heparin salts, citric acid salts, ethylenediaminetetraacetic acid salts, hirudin, sodium pentosan polysulfate, cumarin, derivatives of cumarin, warfarin, or phenprocoumon acenocoumarolor.
Priority: US20070953356P Applic. Date: 2007-08-01
Inventor: MCKALE JAMES M [US]; GIBBS BARBARA S [US]
Application No.: US20090042217A1 Published: 12/Feb/2009Title: Methods and Kits for Determining Blood Coagulation
Applicant/Assignee: RAPPAPORT FAMILY INSTITUTE FOR RESEARCH IN THE MEDICAL SCIENCES
Application No.: 12/223290 Filing Date: 23/Jun/2008
Abstract:A method of determining a coagulation status of a blood sample is provided. The method comprising determining an expression and/or activity ratio of Tissue Factor (TF) to Tissue Factor Pathway Inhibitor (TFPI) in cellular microparticles of the blood sample, wherein the ratio is indicative of the coagulation status of the blood sample.
Priority: US20060762519P Applic. Date: 2006-01-27; WO2007IL00110 Applic. Date: 2007-01-28
Inventor: BRENNER BENJAMIN [IL]; AHARON ANAT [IL]
Application No.: US20090042916A1 Published: 12/Feb/2009Title: [4-(6-FLUORO-7-METHYLAMINO-2,4-DIOXO-1,4-DIHYDRO-2H-QUINAZOLIN-3-YL)-PHENYL]-5-CHLORO-THIOPHEN-2-YL-SULFONYLUREA SALTS, FORMS AND METHODS RELATED THERETO
Applicant/Assignee: PORTOLA PHARMACEUTICALS, INC
Application No.: 12/114742 Filing Date: 02/May/2008
Abstract:The present invention provides novel sulfonylurea salts of a salt of formula (I) and polymorph forms thereof. The compounds in their various forms are effective platelet ADP receptor inhibitors and may be used in various pharmaceutical compositions, and are particularly effective for the prevention and/or treatment of cardiovascular diseases, particularly those diseases related to thrombosis. The invention also provides a method for preparing such compounds and forms and for preventing or treating thrombosis and thrombosis related conditions in a mammal comprising the step of administering a therapeutically effective amount of a salt of formula (I) or a pharmaceutically acceptable form thereof.
Priority: US20070927328P Applic. Date: 2007-05-02
Inventor: SHARP EMMA [GB]; QUEGAN LOUISA JANE [GB]; PANDEY ANJALI [US]; WANG JUAN [US]; NIEDER MATTHEW [US]; HUANG WOLIN [US]
Application No.: US20090043380A1 Published: 12/Feb/2009Title: Coatings for promoting endothelization of medical devices
Applicant/Assignee: SPECIALIZED VASCULAR TECHNOLOGIES, INC
Application No.: 12/128533 Filing Date: 28/May/2008
Abstract:A unique method and coatings are provided for promoting tissue encapsulation of medical devices, especially before antiproliferative drug therapy within a body of a patient in order to prevent excessive restenosis and while avoiding thrombosis (including late stage/stent thrombosis). The method involves delaying the activation of restenosis suppressing (i.e. antiproliferative) drugs in the vicinity of the medical device until a thin layer of geometrically streamlined tissue has deposited itself upon the device. Coatings of one or more layer that provide an aligned scaffolding (i.e. via aligned fibers or aligned grooves) may be used in the method to encourage tissue deposition and/or to delay elution of drug(s) stored beneath or within. The delay phase prior to degradation, erosion, and/or absorption of the coating to release an active drug should last until an optimal amount of controlled restenosis has provided a thin endothelial layer to encapsulate the device.
Priority: US20070964142P Applic. Date: 2007-08-09; US20070993328P Applic. Date: 2007-09-11; US20070002343P Applic. Date: 2007-11-08
Inventor: BLAHA CHARLES MATTHEW [US]; TO JOHN [US]; PHAN LOC X [US]
Application No.: US20090047209A1 Published: 19/Feb/2009Title: Novel nifedipine compositions
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 11/980720 Filing Date: 31/Oct/2007
Abstract:The present invention is directed to nanoparticulate compositions comprising nifedipine. The nifedipine particles of the composition have an effective average particle size of less than about 2 microns.
Priority: US2003-712259 Applic. Date: 2003-11-14; US2003-276400 Applic. Date: 2003-01-15; WO2001US15983 Applic. Date: 2001-05-18; US1999-337675 Applic. Date: 1999-06-22; US2003-345312 Applic. Date: 2003-01-16; US2000-715117 Applic. Date: 2000-11-20; US2002-075443 Applic. Date: 2002-02-15; US2000-666539 Applic. Date: 2000-09-21
Inventor: MERISKO-LIVERSIDGE ELAINE [US]
Application No.: US20090047366A1 Published: 19/Feb/2009Title: Inorganic Coagulation Accelerators for Individuals taking Platelet Blockers or Anticoagulants
Applicant/Assignee:
Application No.: 11/839041 Filing Date: 15/Aug/2007
Abstract:The present invention is a method to accelerate the coagulation of blood through the application of inorganic materials to the wound of a patient on anticoagulant or platelet blocker therapy. The method comprises contacting such wounds with a substance selected from the group consisting of zeolitic molecular sieves and non-zeolitic molecular sieves, diatomaceous earth, glass powder or fibers, precipitated or fumed silica, kaolin and montmorillonite clays and Ca exchanged permutites.
Priority:
Inventor: BEDARD ROBERT L [US]; ZENZ CARL N [US]
Application No.: US20090053245A1 Published: 26/Feb/2009Title: Pharmacokinetics and Efficacy of Anti-Angiogenic Drugs and Drugs Treating Diseases of the Blood
Applicant/Assignee:
Application No.: 12/129487 Filing Date: 29/May/2008
Abstract:A method for modulating at least one pharmacokinetic property of an anti-angiogenic or blood disease or steroid therapeutic and efficacy upon administration to a host is provided. One administers to the host an effective amount of a bifunctional compound of less than about 5000 Daltons comprising the anti-angiogenic or blood disease or steroid therapeutic or an active derivative thereof and a pharmacokinetic modulating moiety. The pharmacokinetic modulating moiety binds to at least one intracellular protein. The bifunctional compound has at least one modulated pharmacokinetic property upon administration to the host as compared to a free drug control that comprises the anticancer therapeutic as well as enhanced efficacy not due to compound degradation. It is preferred that the pharmacokinetic modulating moiety has a mass of less than 1100 Daltons.
Priority: US20070932359P Applic. Date: 2007-05-29
Inventor: MUTZ MITCHELL W [US]; MARQUIS ANDRE L [US]
Application No.: US20090054352A1 Published: 26/Feb/2009Title: BENZENE DERIVATIVE OR SALT THEREOF
Applicant/Assignee: ASTELLAS PHARMA INC
Application No.: 12/091099 Filing Date: 07/Nov/2006
Abstract:Problem: To provide compounds which have an anticoagulation effect based on their ability to inhibit the activated blood coagulation factor X and are useful as coagulation inhibitors or agents for prevention or treatment for diseases caused by thrombi or emboli. Means for Solution: Benzene derivatives or their salts having a characteristic chemical structure with a phenol ring and a benzene ring bonding to each other via an amide bond, in which the phenol ring further bonds to a benzene ring or a heteroaryl ring via an amide bond. They have an excellent effect of inhibiting the activated blood coagulation factor X, and especially have an excellent oral activity.
Priority: JP20050323491 Applic. Date: 2005-11-08; WO2006JP322133 Applic. Date: 2006-11-07
Inventor: HIRAYAMA FUKUSHI [JP]; FUJIYASU JIRO [JP]; KAGA DAISUKE [JP]; NEGORO KENJI [JP]; SASUGA DAISUKE [JP]; SEKI NORIO [JP]; SUZUKI KEN-ICHI [JP]
Application No.: US20090061468A1 Published: 05/Mar/2009Title: REAGENT AND METHOD FOR MEASURING COAGULATION TIME OF BLOOD SAMPLE
Applicant/Assignee: SYSMEX CORPORATION
Application No.: 12/195028 Filing Date: 20/Aug/2008
Abstract:A reagent kit for measuring coagulation time is described herein. This reagent comprises calcium chelator which interferes with the reaction between calcium and substance other than a coagulation factor in a blood sample, and which substantially does not interfere with coagulation reaction. A method for measuring coagulation time is also described herein. The method comprises a contacting step and a measuring step. The contacting step is to contact a blood sample, calcium and compound selected from the group consisting of partial thromboplastin, tissue thromboplastin, and complex of tissue factor and phospholipid, in the presence of calcium chelator. This calcium chelator can interfere with the reaction between calcium and substance other than a coagulation factor in the blood sample and substantially does not interfere with coagulation reaction. The measuring step is to measure coagulation time of the blood sample.
Priority: JP20070226463 Applic. Date: 2007-08-31
Inventor: HOSHIKO SUSUMU [JP]; KOBAYASHI KATSUSHI [JP]
Application No.: US20090068168A1 Published: 12/Mar/2009Title: SUBSTITUTED AMINO ALCOHOLS
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/203581 Filing Date: 03/Sep/2008
Abstract:Disclosed herein are substituted amino alcohol anti-mycobacterial agents and/or chelation therapy agents of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20070970376P Applic. Date: 2007-09-06
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090074718A1 Published: 19/Mar/2009Title: Avian derived erythropoietin
Applicant/Assignee:
Application No.: 11/973853 Filing Date: 10/Oct/2007
Abstract:Erythropoietin obtained from eggs laid by transgenic avians having avian N-linked and O-linked glycosylation patterns.
Priority: US2007-708598 Applic. Date: 2007-02-20; US2006-370555 Applic. Date: 2006-03-08; US2003-351196 Applic. Date: 2003-01-24; US1998-173864 Applic. Date: 1998-10-16; US20070918504P Applic. Date: 2007-03-16; US20060857896P Applic. Date: 2006-11-09; US20060877601P Applic. Date: 2006-12-28; US20060783648P Applic. Date: 2006-03-17; US20060840291P Applic. Date: 2006-08-25; US19970062172P Applic. Date: 1997-10-16
Inventor: IVARIE ROBERT D [US]; HARVEY ALEX J [US]; MORRIS JULIE A [US]; LIU GUODONG [CA]; RAPP JEFFREY C [US]
Application No.: US20090074829A1 Published: 19/Mar/2009Title: Novel Heparin Alternative Material and Method for Producing the Same
Applicant/Assignee:
Application No.: 12/224950 Filing Date: 13/Mar/2007
Abstract:The object is to provide a novel heparin alternative material, which is excellent in safety and in vivo degradability. Disclosed are: a novel heparin alternative material, which comprises an enzymatically synthesized alpha-1,4-glucan derivative and has functions substituting those of heparin, such as an anticoagulation activity and functions of a material for storage or sustained release of a heparin-binding growth factor
a method for production of the substitute material
and a preparation or article for medical applications or a cosmetic produced using the heparin alternative material.
Priority: JP20060069479 Applic. Date: 2006-03-14; WO2007JP54935 Applic. Date: 2007-03-13
Inventor: TANIHARA MASAO [JP]; HOSOYA KAYO [JP]; TAKAHA TAKESHI [JP]; TAKAHARA JUNICHI [JP]; SUNAKO MICHIHIRO [JP]
Application No.: US20090074875A1 Published: 19/Mar/2009Title: Nanoparticulate compositions having lysozyme as a surface stabilizer
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 12/292091 Filing Date: 12/Nov/2008
Abstract:The present invention is directed to nanoparticulate active agent compositions comprising lysozyme as a surface stabilizer. Also encompassed by the invention are pharmaceutical compositions comprising a nanoparticulate active agent composition of the invention and methods of making and using such nanoparticulate and pharmaceutical compositions.
Priority: US2003-357514 Applic. Date: 2003-02-04; US20020353230P Applic. Date: 2002-02-04
Inventor: WERTZ CHRISTIAN F [US]; RYDE NIELS P [US]
Application No.: US20090081297A1 Published: 26/Mar/2009Title: Use of surface tension reducing agents in aerosol formulations
Applicant/Assignee:
Application No.: 11/412523 Filing Date: 27/Apr/2006
Abstract:The present disclosure describes aerosol formulations that are particularly effective for pulmonary aerosol delivery. The aerosol formulations comprise an aqueous dispersion of active agent particles, said aqueous dispersion having an excess of a surface tension reducing agent. As a result of the reduced surface tension of the aqueous dispersion, the resulting aerosol droplets formed have a particle size less in one embodiment of than 10 microns in size or in an alternate embodiment of less than 6 microns in size. The present disclosure also provides for a method for forming an aerosol from said aerosol formulation, a method of treating a mammal in need of said treatment using said aerosol formulation, and a method of diagnosing a mammal in need of such diagnosis using said aerosol formulation.
Priority: US20050675375P Applic. Date: 2005-04-27
Inventor: COOK ROBERT O [US]; ARMER THOMAS A [US]
Application No.: US20090081703A1 Published: 26/Mar/2009Title: METHOD FOR DETECTING DEEP VENOUS THROMBOSIS
Applicant/Assignee:
Application No.: 12/238011 Filing Date: 25/Sep/2008
Abstract:A method for detecting deep vein thrombosis (DVT) in humans includes the steps of assaying a collected blood sample and measuring the amount of Lp-PLA2. The detected amount of Lp-PLA2 is then compared and correlated with known risk values of Lp-PLA2. A diagnosis of a patient's likelihood, risk, or development of DVT may be made by comparing the measured value with values known to correlate to a particular risk or development of DVT.
Priority: US20070975043P Applic. Date: 2007-09-25
Inventor: YALE STEVEN H [US]
Application No.: US20090082800A1 Published: 26/Mar/2009Title: Distal Embolic Protection Devices With A Variable Thickness Microguidewire And Methods For Their Use
Applicant/Assignee: INSERA THERAPEUTICS LLC
Application No.: 11/859272 Filing Date: 21/Sep/2007
Abstract:A distal embolic protection device for dedicated use in cerebral arterial blood vessels is described. The distal embolic protection device comprises a variable-thickness micro-guidewire and a collapsible filtering device mounted on the microguidewire over two mobile attachment points so that in its collapsed configuration, the thickness of the microguidewire and the filtering device at this region is less than or equal to 0.017 inch (0.432 mm) in thickness to be able to pass through existing conventional microcatheters. The mobile attachment points allow for rotatory and longitudinal mobility of the microguidewire while the filtering device is stable thereby decreasing the risk of trauma to the fragile cerebral arterial blood vessels. Preferably, the filtering device comprises an expansion assembly, e.g., a plurality of struts attached to a filter membrane that are in a folded position which self expand to the desired dimensions within the cerebral blood vessels. Also described are methods of using the distal embolic protection devices of this invention.
Priority:
Inventor: JANARDHAN VIKRAM [US]
Application No.: US20090084717A1 Published: 02/Apr/2009Title: MODULAR HEMOFILTRATION APPARATUS WITH REMOVABLE PANELS FOR MULTIPLE AND ALTERNATE BLOOD THERAPY
Applicant/Assignee: TRANSVIVO INC
Application No.: 12/183527 Filing Date: 31/Jul/2008
Abstract:An apparatus for performing blood therapy having a plurality of pumps for engaging blood and fluid tubing is characterized by a plurality of manually mounted and disengagable panels installed on the sides of the apparatus housing, the panels having pump engaging tubing mounted on the inside of the respective panels.
Priority: US20070953577P Applic. Date: 2007-08-02
Inventor: DELMAGE J MICHAEL [US]; PETERS HAROLD [US]; COOPER TOMMY [US]
Application No.: US20090087421A1 Published: 02/Apr/2009Title: Novel Recombinant Staphylokinase Derivatives and the Preparations and Applications thereof
Applicant/Assignee: FUDAN UNIVERSITY
Application No.: 12/185601 Filing Date: 04/Aug/2008
Abstract:The present invention relates to the biotechnology field, more particularly, to novel recombinant staphylokinase (RGD/KGD-Sak) derivatives and the preparation the thereof. The derivatives, have a low polymerizing ability, low immunogenicity and a bifunctionality of thrombolytics and anticoagulant. Based on the line, structural analysis of the monomer and dimer of recombinant staphylokinases and their biochemical properties, we designed two novel bifunctional staphylokinase molecular structures. Mutant genes were constructed by PCR site-directed mutagenesis which were then recombined with a prokaryotic vector and used to transform E. coli. Engineered strains with a high expression level were selected by screening and propagated by fermentation, followed by disruption of the cells, centrifugation to collect inclusion bodies, renaturation, and purification of RGD/KGD-SAK through a two-step method. After lyophilized, the polymerizing ability and immunogenicity of the products decreased significantly. The derivatives can not only activate fibrinogen to lyse thrombus, but also significantly inhibit the platelet aggregation induced by ADP, suggesting that they have the bifunctionality of thrombolytics and anticoagulant.
Priority: CN20001011627 Applic. Date: 2000-01-28; US2003-182160 Applic. Date: 2003-01-22; WO2001CN00102 Applic. Date: 2001-01-23
Inventor: SONG HOUYAN [CN]; SONG GANG [CN]
Application No.: US20090088613A1 Published: 02/Apr/2009Title: CONTINUITY CIRCUITS FOR DETECTING ACCESS DISCONNECTION
Applicant/Assignee: BAXTER INTERNATIONAL INC BAXTER HEALTHCARE S.A
Application No.: 11/862984 Filing Date: 27/Sep/2007
Abstract:A monitor for an extracorporeal therapy access site is disclosed. The monitor includes a bandage atop or adjacent the access site and a sensor for monitoring the bandage. The bandage includes a layer of polymer that expands when wetted with blood. The expansion causes a break in continuity of the sensor, or in an alternate embodiment, causes a sensor to cease detecting a target. When the break occurs, the control circuit monitoring the bandage sends a signal that a break has occurred, and a remote monitor then takes appropriate action, such as ceasing therapy, sending an alert, or sounding an alarm. In another embodiment, connecting wires in a continuity circuit are held apart by a polymer that dissolves when contacted by blood. If a leak occurs and a small portion of the polymer dissolves, the wires make contact, thus detecting a blood leak.
Priority:
Inventor: MARTTILA ALAN W [US]; CHAN WILLIAM W [US]; BHAGTANI REEMA A [US]
Application No.: US20090093697A1 Published: 09/Apr/2009Title: MEMS INTERSTITIAL PROTHROMBIN TIME TEST
Applicant/Assignee:
Application No.: 12/189509 Filing Date: 11/Aug/2008
Abstract:A method of determining a prothrombin time is disclosed. A mediator is applied to a stratum corneum. The stratum corneum is penetrated to allow the mediator to enter a region containing interstitial fluid and interact with at least one capillary, causing blood and/or blood components to leak from the at least one capillary into the region containing interstitial fluid. A characteristic affected by the blood and/or blood components is measured in the region containing interstitial fluid which correlates to the prothrombin time. A system for measuring prothrombin time is also disclosed. The system has a mediator, one or more microneedles, and a processor directly or indirectly coupled to the one or more microneedles and configured to determine a coagulation change in blood or blood components in a region around the one or more microneedles after the one or more microneedles penetrate a stratum corneum.
Priority: US20070955054P Applic. Date: 2007-08-10
Inventor: MIR JOSE [US]; KOWARZ MAREK W [US]; SARBADHIKARI KAMAL K [US]; ASHE PHILIP RYAN [US]
Application No.: US20090093754A1 Published: 09/Apr/2009Title: Device for Treatment of Venous Congestion
Applicant/Assignee:
Application No.: 12/335304 Filing Date: 15/Dec/2008
Abstract:A device for treatment of venous congestion provides for subcutaneous introduction of anticoagulant through an incision positioned within a collection shell for withdrawal of an effused material. A widened delivery tip provides dispersal of the anticoagulant and may be agitated to disrupt clot formation.
Priority: US2002-273215 Applic. Date: 2002-10-16; US2000-745298 Applic. Date: 2000-12-20; US19990171351P Applic. Date: 1999-12-22
Inventor: HARTIG GREGORY K [US]; CONNOR NADINE P [US]; CONFORTI MICHAEL L [US]
Application No.: US20090095679A1 Published: 16/Apr/2009Title: HEMODIALYSIS SYSTEMS AND METHODS
Applicant/Assignee: DEKA PRODUCTS LIMITED PARTNERSHIP
Application No.: 12/199452 Filing Date: 27/Aug/2008
Abstract:Hemodialysis dialysis systems are disclosed. Hemodialysis systems of the invention may include a dialysate flow path including a balancing circuit, a mixing circuit, and/or a directing circuit. The circuits may be defined within one or more cassettes. The fluid circuits may be at least partially isolated, spatially and/or thermally, from electrical components of the system. A gas supply may be provided in fluid communication with the dialysate flow path and/or the dialyzer to urge dialysate through the dialyzer and blood back to the patient. The hemodialysis systems may include fluid handling devices, actuated using a control fluid, optionally delivered using a detachable pump. Fluid handling devices may be generally rigid and of a spheroid shape, optionally with a diaphragm dividing the device into compartments.
Priority: US2008-072908 Applic. Date: 2008-02-27; US20070903582P Applic. Date: 2007-02-27; US20070904024P Applic. Date: 2007-02-27
Inventor: DEMERS JASON A [US]; WILT MICHAEL J [US]; BALLANTYNE TODD A [US]; GRANT KEVIN L [US]; DALE JAMES D [US]
Application No.: US20090098104A1 Published: 16/Apr/2009Title: Method for Diagnosing Cardiovascular Diseases
Applicant/Assignee: MEDIZINISCHE UNIVERSITAT WIEN
Application No.: 12/298209 Filing Date: 16/Apr/2007
Abstract:Method for diagnosing a cardiovascular disease in an individual comprising the steps of: providing a sample of an individual
determining the amount of cytokeratin-18 (CK-18) or fragments thereof and/or interleukin-1beta precursor (IL-1beta precursor) in said sample
comparing the amount of CK-18 or fragments thereof and/or IL-1beta precursor in said sample to the amount of CK-18 or fragments thereof and/or IL-1beta precursor present in a reference control of at least one individual not suffering from a cardiovascular disease
and diagnosing a cardiovascular disease if the amount of CK-18 or fragments thereof in the sample is increased in comparison to the amount of CK-18 or fragments thereof in the reference control and/or the amount of IL-1beta precursor in the sample is decreased in comparison to the amount of IL-1beta precursor in the reference control.
Priority: AT20060000694 Applic. Date: 2006-04-24; WO2007AT00173 Applic. Date: 2007-04-16
Inventor: ANKERSMIT HENDRIK JAN [AT]
Application No.: US20090098119A1 Published: 16/Apr/2009Title: ANTIDOTES FOR FACTOR XA INHIBITORS AND METHODS OF USING THE SAME
Applicant/Assignee: PORTOLA PHARMACEUTICALS, INC
Application No.: 12/239651 Filing Date: 26/Sep/2008
Abstract:The present invention relates antidotes to anticoagulants targeting factor Xa. The antidotes are factor Xa protein derivatives that bind to the factor Xa inhibitors thereby substantially neutralizing them but do not assemble into the prothrombinase complex. The derivatives describe herein lack or have reduced intrinsic coagulant activity. Disclosed herein are methods of stopping or preventing bleeding in a patient that is currently undergoing anticoagulant therapy with a factor Xa inhibitor.
Priority: US20070976343P Applic. Date: 2007-09-28; US20080090574P Applic. Date: 2008-08-20
Inventor: LU GENMIN [US]; PHILLIPS DAVID R [US]; ANDRE PATRICK [US]; SINHA UMA [US]
Application No.: US20090098185A1 Published: 16/Apr/2009Title: Method for treating thrombotic disorders using sulfated polysaccharides
Applicant/Assignee: AVIGEN, INC
Application No.: 12/316632 Filing Date: 15/Dec/2008
Abstract:Methods for treating thrombotic disorders using sulfated polysaccharides such as fucoidans are disclosed.
Priority: US2007-789447 Applic. Date: 2007-04-24; US20060797079P Applic. Date: 2006-04-27
Inventor: JOHNSON KIRK W [US]
Application No.: US20090098585A1 Published: 16/Apr/2009Title: REAGENT KIT FOR DETECTING LUPUS ANTICOAGULANT
Applicant/Assignee: SYSMEX CORPORATION
Application No.: 12/269719 Filing Date: 12/Nov/2008
Abstract:A reagent kit capable of distinguishing between a blood sample containing lupus anticoagulant and blood samples from individuals having other anticoagulant diseases is disclosed. The reagent kit comprises two coagulation time reagents containing phosphatidylserine in a different phosphatidylserine content ratio to the total content of phospholipids from each other, threreby giving different coagulation times with use of corresponding coagulation time reagent.
Priority: JP20020216782 Applic. Date: 2002-07-25; US2003-622736 Applic. Date: 2003-07-21
Inventor: OKUDA MASAHIRO [JP]
Application No.: US20090099639A1 Published: 16/Apr/2009Title: METHOD FOR EXPANSION AND DEPLOYMENT OF POLYMERIC STRUCTURES INCLUDING STENTS
Applicant/Assignee: ARTERIAL REMODELING TECHNOLOGIES, S.A
Application No.: 12/282738 Filing Date: 24/Oct/2007
Abstract:The invention is to methods of deploying polymeric biodegradable or non biodegradable stents by use of stepwise creases in the pressure placed upon the inner diameter of the stent to slowly increase the stent diameter. In one embodiment, the pressure on the interior stent diameter is slowly increased. The stent is allowed to acclimate to this diameter for a set period of time, and then the pressure is again increased. This series of steps continues until the stent reaches its final diameter and a final period of acclimatization is maintained prior to the removal of the deployment/delivery device.
Priority: US20060854075P Applic. Date: 2006-10-25; WO2007IB03195 Applic. Date: 2007-10-24
Inventor: SABARIA PATRICK [FR]
Application No.: US20090104273A1 Published: 23/Apr/2009Title: Novel nifedipine compositions
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LTD
Application No.: 12/292395 Filing Date: 18/Nov/2008
Abstract:The present invention is directed to nanoparticulate compositions comprising nifedipine. The nifedipine particles of the composition have an effective average particle size of less than about 2 microns.
Priority: US2003-712259 Applic. Date: 2003-11-14; US2003-276400 Applic. Date: 2003-01-15; WO2001US15983 Applic. Date: 2001-05-18; US1999-337675 Applic. Date: 1999-06-22
Inventor: MERISKO-LIVERSIDGE ELAINE [US]
Application No.: US20090105629A1 Published: 23/Apr/2009Title: BLOOD CIRCUIT ASSEMBLY FOR A HEMODIALYSIS SYSTEM
Applicant/Assignee: DEKA PRODUCTS LIMITED PARTNERSHIP
Application No.: 12/199077 Filing Date: 27/Aug/2008
Abstract:A blood circuit assembly for a dialysis unit may include an organizing tray, a pair of pneumatic pumps mounted to the organizing tray for circulating blood received from a patient through a circuit including a dialyzer unit and returned to the patient, an air trap mounted to the organizing tray arranged to remove air from blood circulating in the circuit, a pair of dialyzer connections arranged to connect to the inlet and outlet of a dialyzer unit, and a pair of blood line connectors, one inlet blood line connector for receiving blood from the patient and providing blood to the pneumatic pumps and the other outlet blood line connector for returning blood to the patient.
Priority: US2008-120729 Applic. Date: 2008-02-27; US2008-038474 Applic. Date: 2008-02-27; US2007-871821 Applic. Date: 2007-10-12; US2008-038648 Applic. Date: 2008-02-27; US2007-871803 Applic. Date: 2007-10-12; US2007-871793 Applic. Date: 2007-10-12; US2007-871787 Applic. Date: 2007-10-12; US2007-871712 Applic. Date: 2007-10-12; US2007-871680 Applic. Date: 2007-10-12; US20070903582P Applic. Date: 2007-02-27; US20070904024P Applic. Date: 2007-02-27; US20070921314P Applic. Date: 2007-04-02
Inventor: GRANT KEVIN L [US]; DALE JAMES D [US]; WILT MICHAEL J [US]; DEMERS JASON A [US]; COLLINS DAVID E [US]
Application No.: US20090107903A1 Published: 30/Apr/2009Title: Anticoagulant-coated dipstick for use with a blood centrifuge rotor
Applicant/Assignee: IDEXX LABORATORIES, INC
Application No.: 12/290205 Filing Date: 28/Oct/2008
Abstract:An anticoagulant-coated dipstick is selectively receivable by the central fill port of a rotor of a blood centrifuge. The dipstick includes an elongated, rod-like member having a first axial end and an opposite second axial end, and a cap affixed to the second axial end. At least a portion of a surface of the rod-like member is coated with an anticoagulant. The elongated rod-like member of the dipstick is dimensioned in length and diameter to be receivable through the central fill port of the rotor to contact a blood sample contained therein. The cap is circular in shape, with a diameter that is greater than that of the rotor fill port to entirely cover and seal the fill port to prevent leakage therethrough of a blood sample contained in the rotor, especially when the rotor is gently agitated or inverted.
Priority: US20070000849P Applic. Date: 2007-10-29
Inventor: DASSA ALYSSA J [US]
Application No.: US20090110683A1 Published: 30/Apr/2009Title: MONOCLONAL ANTIBODIES AGAINST ACTIVATED PROTEIN C
Applicant/Assignee: OKLAHOMA MEDICAL RESEARCH FOUNDATION
Application No.: 12/257706 Filing Date: 24/Oct/2008
Abstract:The present invention provides monoclonal antibodies that selectively bind to and inhibit activated protein C without binding to or inhibiting unactivated protein C. Other antibodies inhibit both activated protein C and activation of unactivated protein C. Methods of treatment employing these antibodies are described herein as are methods of screening for and detecting these antibodies.
Priority: US20070983092P Applic. Date: 2007-10-26
Inventor: XU JUN [US]; ESMON CHARLES [US]
Application No.: US20090110740A1 Published: 30/Apr/2009Title: Materials and Methods for Modulating Metabolism
Applicant/Assignee:
Application No.: 12/265447 Filing Date: 05/Nov/2008
Abstract:The subject invention provides materials and methods for modulating a variety of biological factors to treat biological conditions associated with the factors. In one embodiment of the invention, a cysteamine compound is administered to a patient to treat hypercholesterolemia and/or complications associated with hypercholesterolemia. In another embodiment, a cysteamine compound is administered to a patient to prevent the onset of diabetes in an at-risk patient and/or treat or prevent the onset of diabetes-associated complications.
Priority: US2005-118737 Applic. Date: 2005-04-29; US20040567899P Applic. Date: 2004-05-03; US20040637618P Applic. Date: 2004-12-20
Inventor: CHAN BILL PIU [CN]; WONG GARY KWAN PO [HK]; XU JINXIAN [CN]; CHI FRANCIS [HK]
Application No.: US20090112049A1 Published: 30/Apr/2009Title: HEART PUMP APPARATUS AND METHOD FOR BEATING HEART SURGERY
Applicant/Assignee: SAUDI ARABIAN OIL COMPANY
Application No.: 11/927160 Filing Date: 29/Oct/2007
Abstract:Apparatus for assisting a surgeon in procedures involving the heart and methods of employing such apparatus are provided. The apparatus can include a pump, and a first fluid conduit having a distal end adapted to be inserted into the superior vena cava of a beating heart, a second fluid conduit having a distal end adapted to be inserted into the inferior vena cava, and a third fluid conduit having a distal end adapted to be inserted into the pulmonary artery of the beating heart, each in liquid fluid communication with the pump, which in combination can be operatively positioned to form a closed cardiac pathway extending from the vena cavae and to the pulmonary artery to thereby convey blood collected from the vena cavae into the pulmonary artery, operatively bypassing the right side of the heart. The pump is positioned to both convey blood flow from each vena cavae and to the third fluid conduit and to provide a blood reservoir which enables the provision of manual assistance to the blood flow to the lungs when blood flow is insufficient.
Priority:
Inventor: AHMED FAYAZ [SA]
Application No.: US20090118660A1 Published: 07/May/2009Title: APPARATUS AND METHOD FOR IN-VIVO PLASMAPHERESIS USING PERIODIC BACKLUSH CONTAINING ANTICOAGULANT
Applicant/Assignee: TRANSVIVO INC
Application No.: 12/353209 Filing Date: 13/Jan/2009
Abstract:Method for in-vivo plasmapheresis utilizing a plurality of elongated hollow microporous filter fibers periodically interrupt diffusion of blood plasma from a patient, and, for a selected time, directing backflush fluid into the fibers at a pressure and interval sufficient to cleanse the fiber pores, after which plasma diffusion is resumed. The backflush fluid, preferably a normal saline solution, may contain an anticoagulant such as heparin, citrate or NO donor in suitable concentration for systemic anti-coagulation or for treating the fiber for thromboresistance.
Priority: US2005-320866 Applic. Date: 2005-12-29; US2003-408657 Applic. Date: 2003-04-04; US2001-754773 Applic. Date: 2001-01-04
Inventor: GORSUCH REYNOLDS G [US]; COOPER TOMMY GENE [US]; HANDLEY JR HAROLD H [US]; PETERS HAROLD W [US]
Application No.: US20090123437A1 Published: 14/May/2009Title: METHODS FOR COLLECTING AND USING PLACENTA CORD BLOOD STEM CELLS
Applicant/Assignee:
Application No.: 12/268319 Filing Date: 10/Nov/2008
Abstract:An innovative method of collecting cord blood stem cells from an isolated mammalian non-exsanguinated or partially exsanguinated placenta by placental perfusion is described and also an easy method for safe long duration cold storage of the placenta. Placental perfusion can include perfusing the isolated placenta with a pulsatile flow of perfusion solution, for example, using a pulsatile or peristaltic pump or device. The stem cells can then be isolated from the perfusate. Significantly increased amounts of CD133+ stem cells can be collected from the perfusate. The perfusion solution can include an anticoagulant. The isolated mammalian placenta need not be treated with an anticoagulant prior to perfusing. The isolated placenta can be free from an anticoagulant prior to perfusing.
Priority: WO2007US11359 Applic. Date: 2007-05-11; US20060799734P Applic. Date: 2006-05-11
Inventor: TAKEBE NAOKO [US]
Application No.: US20090123907A1 Published: 14/May/2009Title: LYSINE CITRATE FOR PLASMA PROTEIN AND DONOR PROTECTION
Applicant/Assignee: SHANBROM TECHNOLOGIES, LLC
Application No.: 11/914532 Filing Date: 22/Jul/2005
Abstract:An improved anticoagulant or additive is based on a higher level of citric acid than is usual (at least about 1.0% weight by volume). The higher citrate is combined with an amino acid as a counterion. The amino acid prevents cellular damage often caused by elevated citrate levels. The amino acid citrate mixture also serves to preserve platelet concentrates and platelet rich plasma during room incubation. Not only does the amino acid citrate combination enhance platelet integrity, it completely inhibits or kills bacteria such as Staphylococcus epidermidis. Collecting blood of plasma into such higher levels of citrate prevents activation of blood proteins so that fractions made from the blood or plasma have superior characteristics.
Priority: US2004-897632 Applic. Date: 2004-07-22; WO2005US26308 Applic. Date: 2005-07-22
Inventor: SHANBROM EDWARD [US]
Application No.: US20090124954A1 Published: 14/May/2009Title: APPARATUS AND METHOD FOR AUTOLOGOUS NORMOVOLEMIC HEMODILUTION
Applicant/Assignee: UNIVERSITY HOSPITALS OF CLEVELAND
Application No.: 12/355275 Filing Date: 16/Jan/2009
Abstract:A system and method for autologous normovolemic hemodilution (ANH) are disclosed. The system can include a vacuum canister, which is sized to accept donor bags of a predetermined capacity. The vacuum canister is connected to a vacuum source which applies a suction to the donor bag within the canister. The system can include a canister having a self-generated vacuum, which includes compressible sidewalls that are spring-loaded to provide negative pressure needed to collect blood from a patient without the use of a gravity-induced siphon gradient. Also disclosed are ANH systems and kits that rely on a gravity-induced siphon gradient for blood collection.
Priority: US2005-318286 Applic. Date: 2005-12-23; US20040639246P Applic. Date: 2004-12-27
Inventor: TRICKETT JAMES R [US]
Application No.: US20090129976A1 Published: 21/May/2009Title: Circuit For Collecting Blood Component And Apparatus For Collecting Blood Component
Applicant/Assignee:
Application No.: 11/988105 Filing Date: 04/Jul/2006
Abstract:A circuit for collecting a blood component includes a blood collection device provided with a blood collection needle through which blood is collected from a blood donor, a blood separator in which the blood collected by the above blood collection device is separated, a blood component collection bag in which a predetermined blood component separated by the above blood separator is collected, a blood line in which the blood collection needle is connected to an inlet of the blood separator, a line for removing an initial blood flow, which branches from a first branching portion formed in the blood line, and in which an initial flow of blood collected from the blood donor is removed, and an anticoagulant-injection line that branches from a second branching portion, formed in the line for removing the initial blood flow, and into which an anticoagulant is injected.
Priority: JP20050200623 Applic. Date: 2005-07-08; WO2006JP313328 Applic. Date: 2006-07-04
Inventor: HOSHINO YOSHITERU [JP]; YOKOO YOSHIHIRO [JP]; YAMAZAKI YUUSUKE [JP]
Application No.: US20090130104A1 Published: 21/May/2009Title: FUSION PROTEINS FOR INHIBITION AND DISSOLUTION OF COAGULATION
Applicant/Assignee: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Application No.: 12/089250 Filing Date: 05/Oct/2006
Abstract:Fusion proteins containing a ligand which specifically binds to a selected vascular bed linked to an anti-thrombotic molecule are provided. Also provided are methods for use of these fusion proteins to prevent coagulation, to dissolve blood clots and to protect against the risk of iatrogenic side effects including those arising from cancer therapy and specific vascular occluding agents.
Priority: US20050723899P Applic. Date: 2005-10-05; WO2006US38989 Applic. Date: 2006-10-05
Inventor: MUZYKANTOV VLADIMIR R [US]; GOTTSTEIN CLAUDIA [US]; DING BI-SEN [US]; CINES DOUGLAS B [US]
Application No.: US20090130293A1 Published: 21/May/2009Title: BIOCOMPATIBLE COATINGS FOR MEDICAL DEVICES
Applicant/Assignee:
Application No.: 11/941834 Filing Date: 16/Nov/2007
Abstract:Biocompatible coatings for implantable medical devices are disclosed. Embodiments of the invention provide plasma etch processes, surface silanization processes, and protein coating processes. Embodiments of the invention provide tropoelastin coatings and methods of creating tropoelastin coatings for implantable medical devices. Optionally, the biocompatible coating can be a drug eluting coating.
Priority:
Inventor: SHYKIND DAVID [US]; YOUNKIN TODD [US]; BURGHARD JOHN [US]; KUHN MARKUS [US]; CAMPBELL CARMEN [US]; MAIZ JOSE [US]
Application No.: US20090131847A1 Published: 21/May/2009Title: System and device for medically treating an individual
Applicant/Assignee:
Application No.: 12/288905 Filing Date: 24/Oct/2008
Abstract:A system for medically treating/vaccinating an individual comprising a first syringe, containing an anticoagulant material therein, for drawing a sample of blood from the individual. A centrifuge means for centrifuging the sample of blood contained within the first syringe to obtain a buffy coat. A second syringe comprising a second plunger and at least one microtubule member containing one of a treatment agent and a vaccine antigen. At least one open end formed within the at least one microtubule member for drawing a portion of the buffy coat therein and exposing the buffy coat to one of the treatment agent and vaccine antigen. A second needle capable of being attached onto the second syringe for introducing the exposed sample into the individual to effect treatment/vaccination thereof.
This system is capable of allowing a plurality of treatment agents and/or vaccine antigens to be simultaneously applied to an individual.
Priority: US2006-507876 Applic. Date: 2006-08-22
Inventor: NALIN DAVID R [US]
Application No.: US20090138070A1 Published: 28/May/2009Title: Stent Apparatuses for Treatment Via Body Lumens and Methods of Use
Applicant/Assignee: INSPIREMD LTD
Application No.: 11/920972 Filing Date: 24/May/2006
Abstract:An enhanced stent apparatus, comprising: a support element, wherein the support element is constructed to be positioned in a body lumen
and, a porous structure, the porous structure located on a surface of the support element, and wherein the porous structure is comprised of at least one fiber under 30 microns in diameter, has a coverage area of less than 30% and is provided with apertures.
Priority: US20050683788P Applic. Date: 2005-05-24; US20050716100P Applic. Date: 2005-09-12; US20050742460P Applic. Date: 2005-12-05; WO2006IB51874 Applic. Date: 2006-05-24
Inventor: HOLZER ZEEV ASHER [IL]; PAZ OFIR [IL]; BAR ELI [IL]; COHEN ILANA [IL]
Application No.: US20090143572A1 Published: 04/Jun/2009Title: METHOD FOR SEPERATING AND PURIFYING RNA
Applicant/Assignee:
Application No.: 11/995310 Filing Date: 30/Aug/2006
Abstract:A method for separating and purifying RNA including the steps of passing a sample solution containing a nucleic acid, a washing solution and a recovering solution through a nucleic acid-adsorbing porous membrane to adsorb nucleic acid, adsorbing, washing and recovering, in which the nucleic acid adsorbing porous membrane is a porous membrane capable of adsorbing a nucleic acid by interaction involving substantially no ionic bond, and the sample solution is obtained by a process, comprising the steps of (I) injecting a test sample containing at least one of blood and leukocyte, and further containing an anticoagulant to a container, (II) adding a hemolytic agent to the container to obtain a leukocyte pallet, (III) adding a nucleic acid-solubilizing reagent to the leukocyte pallet to obtain a mixture solution and (IV)
adding a water-soluble organic solvent to the mixture solution to obtain the sample solution containing the nucleic acid.
Priority: JP20050249694 Applic. Date: 2005-08-30; JP20060229142 Applic. Date: 2006-08-25; WO2006JP317584 Applic. Date: 2006-08-30
Inventor: INOMATA HIROKO [JP]; MORI TOMOKO [JP]
Application No.: US20090148383A1 Published: 11/Jun/2009Title: Anticoagulation Agent and Uses Thereof
Applicant/Assignee: BAKER MEDICAL RESEARCH INSTITUTE BAKER IDI HEART & DIABETES INSTITUTE HOLDINGS LIMITED
Application No.: 11/988196 Filing Date: 05/Jul/2006
Abstract:The present invention provides an anticoagulant agent including a first element capable of inhibiting coagulation and a second element capable of targeting an activated platelet wherein upon administration of element directs the first element to the activated platelet. Also provided is a probe for detecting a blood vessel abnormality including (a) a binding element capable of targeting an activated platelet and (b) a label. Applicant has shown that agents and probes directed to activated platelets are useful in the diagnosis and therapy of coagulation disorders.
Priority: AU20050903570 Applic. Date: 2005-07-05; AU20050905522 Applic. Date: 2005-10-06; WO2006AU00943 Applic. Date: 2006-07-05
Inventor: PETER KARLHEINZ [AU]
Application No.: US20090148502A1 Published: 11/Jun/2009Title: COMPOSITIONS AND METHODS FOR TREATING LACERATIONS, ABRASIONS, AVULSIONS, BURNS, ULCERS, AND CASES OF EXCESSIVE BLEEDING
Applicant/Assignee: HEMO NANOSCIENCE, LLC
Application No.: 11/876343 Filing Date: 22/Oct/2007
Abstract:Described herein are compositions and methods related to wound treatment. Compositions are multi-components admixed in amounts and ratios to meet specific objectives for optimally treating various types of wound injury.
Priority: US20060853621P Applic. Date: 2006-10-23
Inventor: PRONOVOST ALLAN D [US]
Application No.: US20090149728A1 Published: 11/Jun/2009Title: BLOOD CONTACTING SENSOR
Applicant/Assignee: MEDTRONIC MINIMED, INC
Application No.: 12/264810 Filing Date: 04/Nov/2008
Abstract:The invention provides methods and apparatus for detecting an analyte in blood. The apparatus is particularly suited for bringing a sensor into direct contact with blood in vivo. The apparatus comprises a sensor that detects the presence of an analyte and an assembly means. The assembly means has a sensor end, wherein the sensor end of the assembly means is affixed to the sensor, and the assembly means is adapted for coupling with a venous flow device. By coupling with a venous flow device, the assembly means brings the sensor into direct contact with blood flowing through the venous flow device. Examples of venous flow devices that bring the sensor into direct contact with the blood of a subject include, but are not limited to, intravenous catheters and external blood loops, such as are used in extra corporeal membrane oxygenation or hemodialysis.
Priority: US2004-935954 Applic. Date: 2004-09-08
Inventor: VAN ANTWERP NANNETTE M [US]; ENEGREN BRADLEY J [US]; MASTROTOTARO JOHN J [US]; SHAH RAJIV [US]; HOSS UDO [US]; ZHANG YANAN [US]; WANG JENN-HANN [US]; CLARK KENT L [US]
Application No.: US20090155838A1 Published: 18/Jun/2009Title: Devices, systems and methods for the collection, stimulation, stabilization, and analysis of a biological sample
Applicant/Assignee: SMART TUBE, INC
Application No.: 12/315186 Filing Date: 28/Nov/2008
Abstract:Devices, systems, methods and kits for the collection, stimulation, stabilization and analysis of biological samples, including blood samples, are disclosed. An embodiment of the invention includes a container having a side wall, a bottom wall and a closure member defining an internal compartment having arranged therein a partition defining and fluidly separating first and second chambers in the internal compartment, the first chamber positioned in association with the closure member to receive the biological sample
in which at least one wall is constructed of an elastically deformable material
in which the first chamber contains at least one stimulating agent
in which the second chamber contains at least one stabilizing agent
and in which the first and second chambers can be placed in fluid communication by a user without opening or otherwise compromising the fluid integrity of the internal compartment.
Priority: US20070990626P Applic. Date: 2007-11-28
Inventor: HALE MATTHEW [US]
Application No.: US20090156504A1 Published: 18/Jun/2009Title: METHODS OF TREATING BLOOD CELL DEPLETION
Applicant/Assignee: IMMUNEREGEN BIOSCIENCES, INC
Application No.: 12/179409 Filing Date: 24/Jul/2008
Abstract:Provided herein are methods and compositions useful for the replenishment of blood cells in a mammal after exposure to therapeutic radiation or drugs. Radiation illness can be reduced in animals by treatment with substance P analogs. In one embodiment, granulocytes can be regenerated after therapeutic radiation by the administration of a substance P analog. In one embodiment, substance P analogs are useful for reducing PARP activity or PARP expression. In one embodiment, substance P analogs are useful for preventing, reducing or ameliorating adverse effects of drugs. In one embodiment, drug induced blood dyscrasias can be ameliorated by the methods and compositions provided herein.
Priority: US20070966948P Applic. Date: 2007-08-29; US20070965580P Applic. Date: 2007-08-20; US20070952691P Applic. Date: 2007-07-30; US20080039866P Applic. Date: 2008-03-27; US20080039860P Applic. Date: 2008-03-27
Inventor: SIEGEL HAL [US]; WILHELM MICHAEL K [US]
Application No.: US20090157057A1 Published: 18/Jun/2009Title: Circulatory monitoring systems and methods
Applicant/Assignee: SEARETE LLC, A LIABILITY CORPORATION OF THE STATEOF DELAWARE
Application No.: 12/154140 Filing Date: 19/May/2008
Abstract:Systems and methods are described for obtaining and acting upon information indicative of circulatory health and related phenomena in human beings or other subjects. Some involve implementing or deploying therapeutic administration systems, for example, for obtaining a priori implant information and signaling a decision whether to initiate implant-site-targeting treatment partly based on the a priori implant information and partly based on one or more other clot-indicative determinants
or obtaining a flow-change-indicative measurement and signaling a decision whether to administer one or more clot-reducing agents at least partly based on the flow-change-indicative measurement
or obtaining one or more indications of a lytic material in a vicinity of one or more body lumens and accelerating a decrease in a local concentration of the lytic material in the vicinity of the one or more body lumens by causing one or more elements to extract at least a portion of the lytic material in the vicinity of the one or more body lumens in response to the one or more indications of the lytic material in the vicinity of the one or more body lumens
or one or more capture components configured to accelerate a decrease in a local concentration of one or more therapeutic structures along a downstream portion of a vasculature and one or more dispensation components configured to release the one or more therapeutic structures into an upstream portion of the vasculature.
Priority: US2007-004107 Applic. Date: 2007-12-18; US2008-154138 Applic. Date: 2008-05-19; US2008-154162 Applic. Date: 2008-05-19; US2008-152669 Applic. Date: 2008-05-14; US2008-152846 Applic. Date: 2008-05-15; US2008-154654 Applic. Date: 2008-05-22
Inventor: FERREN BRAN [US]; HAGEN JEFFREY JOHN [US]; HYDE RODERICK A [US]; ISHIKAWA MURIEL Y [US]; LEUTHARDT ERIC C [US]; RIVET DENNIS J [US]; WOOD JR LOWELL L [US]; WOOD VICTORIA Y H [US]
Application No.: US20090163548A1 Published: 25/Jun/2009Title: Method of using and comopositions comprising immunomodulatory compounds for the treatment and management of myeloproliferative diseases
Applicant/Assignee:
Application No.: 11/579352 Filing Date: 22/Sep/2008
Abstract:Methods of treating, preventing and/or managing a myeloproliferative disease are disclosed. Specific methods encompass the administration of an immunomodulatory compound, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof, alone or in combination with a second active agent, and/or the transplantation of blood or cells. Particular second active agents are capable of suppressing the overproduction of hematopoietic stem cells or ameliorating one or more of the symptoms of a myeloproliferative disease. Pharmaceutical compositions, single unit dosage forms, and kits suitable for use in methods of the invention are also disclosed.
Priority: WO2004US14003 Applic. Date: 2004-05-05
Inventor: ZELDIS JEROME B [US]
Application No.: US20090163856A1 Published: 25/Jun/2009Title: Treatment indications informed by a prior implant information
Applicant/Assignee: SEARETE LLC, A LIMITED LIABILITY CORPORATION OF THE STATE OF DELAWARE
Application No.: 12/004453 Filing Date: 19/Dec/2007
Abstract:Systems and methods are described for implementing or deploying therapeutic administration systems for obtaining a priori implant information and signaling a decision whether to initiate implant-site-targeting treatment partly based on the a priori implant information and partly based on one or more other clot-indicative determinants
or obtaining a flow-change-indicative measurement and signaling a decision whether to administer one or more clot-reducing agents at least partly based on the flow-change-indicative measurement
or obtaining one or more indications of a lytic material in a vicinity of one or more body lumens and accelerating a decrease in a local concentration of the lytic material in the vicinity of the one or more body lumens by causing one or more elements to extract at least a portion of the lytic material in the vicinity of the one or more body lumens in response to the one or more indications of the lytic material in the vicinity of the one or more body lumens
or one or more capture components configured to accelerate a decrease in a local concentration of one or more therapeutic structures along a downstream portion of a vasculature and one or more dispensation components configured to release the one or more therapeutic structures into an upstream portion of the vasculature.
Priority:
Inventor: FERREN BRAN [US]; HYDE RODERICK A [US]; ISHIKAWA MURIEL Y [US]; LEUTHARDT ERIC C [US]; RIVET DENNIS J [US]; WOOD JR LOWELL L [US]; WOOD VICTORIA Y H [US]
Application No.: US20090169545A1 Published: 02/Jul/2009Title: 5-HT4 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF HEART FAILURE
Applicant/Assignee: SERODUS AS
Application No.: 12/372592 Filing Date: 17/Feb/2009
Abstract:This invention provides the use of a 5-HT4 receptor antagonist in the manufacture of a medicament for treating or preventing heart failure. Particular heart disorders to be treated are selected from the group comprising chronic heart failure, congestive heart failure, chronic congestive heart failure and heart failure resulting from ischaemic heart disease. Methods of treating heart failure using 5-HT4 receptor antagonists and pharmaceutical compositions containing 5-HT4 receptor antagonists are also provided.
Priority: GB20020011230 Applic. Date: 2002-05-16; US2005-514386 Applic. Date: 2005-08-26; WO2003GB02134 Applic. Date: 2003-05-16
Inventor: LEVY FINN OLAV [NO]
Application No.: US20090169620A1 Published: 02/Jul/2009Title: ORALLY DISINTEGRATING TABLET COMPOSITIONS OF TEMAZEPAM
Applicant/Assignee:
Application No.: 12/339908 Filing Date: 19/Dec/2008
Abstract:The compositions of the present invention are orally disintegrating tablet compositions comprising a therapeutically effective amount of at least one drug such as temazepam, 0.5-3% of an ODT binder polymer, a sugar alcohol and/or saccharide, and a disintegrant.
Priority: US20070015931P Applic. Date: 2007-12-21
Inventor: VENKATESH GOPI M [US]; CLEVENGER JAMES M [US]; LAI JIN-WANG [US]; PUROHIT VIVEK [US]
Application No.: US20090169714A1 Published: 02/Jul/2009Title: BIOCOMPATIBLE COATINGS FOR MEDICAL DEVICES
Applicant/Assignee:
Application No.: 11/964428 Filing Date: 26/Dec/2007
Abstract:Biocompatible coatings for implantable medical devices are disclosed. Embodiments of the invention provide methods for coating an object with a biocompatible coating wherein the device is suspended using a flowing gas during the coating process. Embodiments of the invention provide tropoelastin coatings and methods of creating tropoelastin coatings for implantable medical devices. Optionally, the biocompatible coating can be a drug eluting coating.
Priority:
Inventor: BURGHARD JOHN [US]; CAMPBELL CARMEN [US]; YOUNKIN TODD R [US]; KUHN MARKUS [US]; SHYKIND DAVID [US]; MAIZ JOSE [US]
Application No.: US20090170932A1 Published: 02/Jul/2009Title: DISINFECTANT COMPOSITIONS, METHODS AND SYSTEMS
Applicant/Assignee: TYCO HEALTHCARE GROUP LP
Application No.: 12/347073 Filing Date: 31/Dec/2008
Abstract:Disinfectant compositions comprising N-Acetyl Cysteine (NAC) and Vitamin C are disclosed. The disinfectant compositions have also demonstrated activity in inhibiting as well as killing micro-organisms responsible for generating biofilms. They are safe for human and medical uses and may be used as prophylactic preparations to reduce the proliferation of and/or eliminate existing or established infections.
Priority: US20070006201P Applic. Date: 2007-12-31
Inventor: AGGARWAL DINESH [US]; SHAH CHIRAG [US]
Application No.: US20090171303A1 Published: 02/Jul/2009Title: Fixed- or Variable-Length, Wire-Reinforced Catheter and Method of Adaptation
Applicant/Assignee:
Application No.: 12/343888 Filing Date: 24/Dec/2008
Abstract:This disclosure relates to a fixed- or variable-length, wire-reinforced catheter for use in a human body or connected to a subcutaneous port implanted in a human body for use under a cyclical internal load and method of adaptation thereof, and more particularly, to a wire-reinforced catheter of increased internal diameter or reduced external diameter of fixed or variable lengths for the optimized transportation of blood under cyclical internal load and without damage.
Priority: US20070017095P Applic. Date: 2007-12-27
Inventor: LOITERMAN DAVID A [US]; LOITERMAN MICHAEL G [US]
Application No.: US20090171448A1 Published: 02/Jul/2009Title: Implantable device with miniature rotating portion for energy harvesting
Applicant/Assignee:
Application No.: 11/976434 Filing Date: 24/Oct/2007
Abstract:A miniature rotating portion, anchored to and used within the human body. Optionally and preferably, the device may be used to generate energy for sensors or other implantable devices.
Priority: US20070924041P Applic. Date: 2007-04-27
Inventor: ELI URI [IL]
Application No.: US20090173158A1 Published: 09/Jul/2009Title: MEASUREMENT CHAMBER AND RESONATOR
Applicant/Assignee: ANDREAS HETTICH GMBH & CO., KG
Application No.: 12/294959 Filing Date: 28/Mar/2007
Abstract:The invention relates to an apparatus comprising a measurement chamber and a resonator, which can be integrated in the measurement chamber via a quick-action closure, for the liquid sensor system and for verification and measurement of the concentration of materials, substances, particles and/or microorganisms in liquids. The invention is characterized in that the resonator is held only on its outer circumference by a thin elastomer ring, and in that at the radial distance of the external diameter of the resonator, the elastomer ring on the one hand rests on an upper sealing ring of the measurement chamber, forming a seal, and on the other hand rests on a holding ring.
Priority: DE200610015512 Applic. Date: 2006-03-31; WO2007EP02729 Applic. Date: 2007-03-28
Inventor: GEHRING FRANK K [DE]
Application No.: US20090173641A1 Published: 09/Jul/2009Title: AUTOMATED METHOD AND APPARATUS FOR DETECTING ERRONEOUS SAMPLE COLLECTION IN CLINICAL ASSAYS
Applicant/Assignee: ABBOTT POINT OF CARE INC
Application No.: 12/339886 Filing Date: 19/Dec/2008
Abstract:A method for identifying biological samples that are collected using the wrong anticoagulant for subsequent analytical testing. The method also provides for identification of certain analytical test results that are substantially or partly adversely affected.
Priority: US20070015582P Applic. Date: 2007-12-20
Inventor: BROUWER ERIC [CA]; TIRINATO JODY ANN [US]; ZELIN MICHAEL P [US]
Application No.: US20090176758A1 Published: 09/Jul/2009Title: LACTAM-CONTAINING COMPOUNDS AND DERIVATIVES THEREOF AS FACTOR XA INHIBITORS
Applicant/Assignee: BRISTOL-MYERS SQUIBB COMPANY
Application No.: 12/401401 Filing Date: 10/Mar/2009
Abstract:The present application describes lactam-containing compounds and derivatives thereof of Formula I: P4-P-M-M4 I or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
Priority: US2007-955678 Applic. Date: 2007-12-13; US2005-198801 Applic. Date: 2005-08-05; US2004-850587 Applic. Date: 2004-05-20; US2002-245122 Applic. Date: 2002-09-17; US20010324165P Applic. Date: 2001-09-21; US20020402317P Applic. Date: 2002-08-09
Inventor: PINTO DONALD J P [US]; QUAN MIMI L [US]; ORWAT MICHAEL J [US]; LI YUN-LONG [US]; HAN WEI [US]; QIAO JENNIFER X [US]; LAM PATRICK Y S [US]; KOCH STEPHANIE L [US]
Application No.: US20090176792A1 Published: 09/Jul/2009Title: SUBSTITUTED DIBENZHYDRYLPIPERAZINES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/350032 Filing Date: 07/Jan/2009
Abstract:The present invention relates to new dibenzhydrylpiperazine modulators of histamine receptors, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080019520P Applic. Date: 2008-01-07
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090181895A1 Published: 16/Jul/2009Title: Stabilised Compositions of Factor VII Polypeptides
Applicant/Assignee: NOVO NORDISK HEALTH CARE AG
Application No.: 12/407266 Filing Date: 19/Mar/2009
Abstract:The invention relates to chemically as well as physically stable kits and compositions comprising polypeptides, in particular Factor VII or Factor VII-related polypeptides, such that these compositions can be stored, handled and used at room temperature.
Priority: DK20030001901 Applic. Date: 2003-12-19; US2006-450783 Applic. Date: 2006-06-09; WO2004EP53587 Applic. Date: 2004-12-17; US20030531728P Applic. Date: 2003-12-22
Inventor: HANSEN BIRTHE LYKKEGAARD [DK]; JENSEN MICHAEL BECH [DK]; KORNFELT TROELS [DK]
Application No.: US20090191177A1 Published: 30/Jul/2009Title: Enantiomerically Pure (-) 2-[1-(7-methyl-2-(morpholin-4-yl)-4-oxo-4H-pyrido[1,2-A]pyrimidin-9-yl)ethylamino]benzoic Acid, Its Use In Medical Therapy, And A Pharmaceutical Composition Comprising It - 026
Applicant/Assignee:
Application No.: 12/359323 Filing Date: 25/Jan/2009
Abstract:The present invention relates to enantiomerically pure (-) 2-[1-(7-methyl-2-(morpholin-4-yl)-4-oxo-4H-pyrido[1,2-a]pyrimidin-9-yl)ethylamino]benzoic acid or pharmaceutically acceptable salts thereof, it being in a solid state, its use in medical therapy, pharmaceutical composition comprising it, its use in the preparation of a medicament for use in a method for preventing or treating diseases, and its use in method for preventing or treating disease. The present invention relates to a selective inhibitor of phosphoinositide (PI) 3-kinase beta and use of the selective inhibitor in e.g. anti-thrombotic therapy.
Priority: US20080023498P Applic. Date: 2008-01-25
Inventor: FJELLSTROM OLA [SE]; GUSTAFSSON DAVID [SE]; LINDBERG JAN A [SE]; JACKSON SHAUN [AU]
Application No.: US20090191183A1 Published: 30/Jul/2009Title: SUBSTITUTED INDOLES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/181929 Filing Date: 29/Jul/2008
Abstract:Disclosed herein are substituted indole cysteinyl leukotriene receptor modulators of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20070952862P Applic. Date: 2007-07-30
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090191637A1 Published: 30/Jul/2009Title: Method and apparatus for determining anticoagulant therapy factors
Applicant/Assignee:
Application No.: 12/378456 Filing Date: 14/Feb/2009
Abstract:Methods and apparatus are disclosed for determining a new anticoagulant therapy factors for monitoring oral anticoagulant therapy to help prevent excessive bleeding or deleterious blood clots that might otherwise occur before, during or after surgery. New anticoagulant therapy factors maybe based upon the time to maximum acceleration from the time of reagent injection (TX) into a plasma sample, Embodiments include methods and apparatus for determining an anticoagulant therapy factor without requiring use of a mean normal prothrombin time determination or ISI, and may be carried out with the patient sample and a coagulation reagent.
Priority: US2007-906325 Applic. Date: 2007-10-01; US2006-359667 Applic. Date: 2006-02-22; US2003-662043 Applic. Date: 2003-09-12; US2003-428708 Applic. Date: 2003-05-02; US20050679423P Applic. Date: 2005-05-10
Inventor: CARROLL WALLACE E [US]; JACKSON R DAVID [US]
Application No.: US20090192597A1 Published: 30/Jul/2009Title: Surgical implant, method for the production and use thereof
Applicant/Assignee: AESCULAP AG & CO. KG
Application No.: 12/385045 Filing Date: 30/Mar/2009
Abstract:A surgical implant is made from biocompatible fiber material as a woven textile fabric, in particular in the form of a vascular prosthesis, the woven fabric being so configured that its permeability to blood is so low that the blood impregnates the textile fabric upon implantation and seals it off by coagulating, but does not flow through it.
Priority: DE20011025712 Applic. Date: 2001-05-21; US2004-478128 Applic. Date: 2004-04-30; WO2002EP05544 Applic. Date: 2002-05-21
Inventor: BENTELE FRANZ [DE]; GOLDMANN HELMUT [DE]
Application No.: US20090196928A1 Published: 06/Aug/2009Title: Biocompatible hydrogel compositions
Applicant/Assignee:
Application No.: 12/384699 Filing Date: 08/Apr/2009
Abstract:Compositions, instruments, systems, and methods are providing for creating families of materials having diverse therapeutic indications and possessing enhanced biocompatibility. One genus platform for the families includes a biocompatible synthetic electrophilic component mixed with a nucleophilic component. The electrophilic component can include a functionalized electrophilic poly (anhydride ester) material. The nucleophilic material can include a natural, autologous protein. The components, when mixed in a liquid state, react by cross-linking, forming a solid matrix composition, or hydrogel.
Priority: US2005-233737 Applic. Date: 2005-09-23; US2004-948765 Applic. Date: 2004-09-23
Inventor: HNOJEWYI OLEXANDER [US]
Application No.: US20090202540A1 Published: 13/Aug/2009Title: SUBSTITUTED OXAZAPHOSPHORINES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/368754 Filing Date: 10/Feb/2009
Abstract:The present invention relates to new oxazaphosphorine alkylating agents and/or immuno-suppressive agents, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080027775P Applic. Date: 2008-02-11
Inventor: GANT THOMAS G [US]
Application No.: US20090203656A1 Published: 13/Aug/2009Title: Method for the Reduction of Dangerous Blood Sugar Levels
Applicant/Assignee:
Application No.: 12/069505 Filing Date: 11/Feb/2008
Abstract:The present invention relates to a method and procedure for reducing immediate serum glucose levels without resort to drugs. Specifically, the invention discloses a regular regimen comprising modest exercise, daily nutritional supplements and a series of specific, time sensitive steps, which, when followed will optimize the effects of the invention.
Priority:
Inventor: RUSSEL KENNETH O [US]
Application No.: US20090203763A1 Published: 13/Aug/2009Title: SUBSTITUTED BENZHYDRYLETHERS
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/357996 Filing Date: 22/Jan/2009
Abstract:Disclosed herein are substituted benzhydrylethers of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of their use thereof.
Priority: US20080022667P Applic. Date: 2008-01-22
Inventor: GANT THOMAS G [US]
Application No.: US20090209031A1 Published: 20/Aug/2009Title: MEDICAL DEVICE PACKAGE
Applicant/Assignee: TYCO HEALTHCARE GROUP LP
Application No.: 12/431837 Filing Date: 29/Apr/2009
Abstract:A package for a medical device, the package capable of sustaining viable cells, wherein the package includes a first container, which is configured to receive a medical device and to sustain at least one viable cell, and a fluid port in communication with the first container for allowing sterile passage of an agent to the medical device and for maintaining cell viability.
Priority: US2007-954426 Applic. Date: 2007-12-12; US2006-340912 Applic. Date: 2006-01-26; US20080049504P Applic. Date: 2008-05-01
Inventor: STOPEK JOSHUA B [US]
Application No.: US20090209550A1 Published: 20/Aug/2009Title: SUBSTITUTED TRIAZOLOPYRIDINES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/389561 Filing Date: 20/Feb/2009
Abstract:Disclosed herein are substituted triazolopyridine serotonin reuptake modulators and/or 5-HT receptor modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080029960P Applic. Date: 2008-02-20
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090209933A1 Published: 20/Aug/2009Title: WHOLE BLOOD COLLECTION KIT AND METHOD
Applicant/Assignee: ASSUREIMMUNE, LLC
Application No.: 12/032124 Filing Date: 15/Feb/2008
Abstract:A blood collection device includes a collection container, a flexible conduit permanently affixed at a proximal end to the collection container, and a needle permanently affixed to a distal end of the flexible conduit. The collection container, flexible conduit and needle can be provided within a package. A method for collecting blood products is also disclosed.
Priority:
Inventor: ZYLBERBERG JAVIER [US]; ZYLBERBERG CLAUDIA [US]; GILCHER RONALD O [US]
Application No.: US20090214675A1 Published: 27/Aug/2009Title: 4-Chromenonyl-1,4-dihydropyridinecarbonitriles and the use thereof
Applicant/Assignee: BAYER HEALTHCARE AG
Application No.: 11/989279 Filing Date: 14/Jul/2006
Abstract:The present application relates to novel 4-chromenonyl-1,4-dihydropyridinecarbonitriles, processes for their preparation, pharmaceutical compositions containing them, and their use for the treatment and/or prophylaxis of diseases, especially cardiovascular disorders.
Priority: DE200510034264 Applic. Date: 2005-07-22; WO2006EP06905 Applic. Date: 2006-07-14
Inventor: KUHL ALEXANDER [DE]; KOLKHOF PETER [DE]; HECKROTH HEIKE [DE]; SCHLEMMER KARL-HEINZ [DE]; FLAMME INGO [DE]; FIGUEROA PEREZ SANTIAGO [DE]; GIELEN-HAERTWIG HEIKE [DE]; GROSSER ROLF [DE]; ERGUEDEN JENS-KERIM [DE]; LANG DIETER [DE]
Application No.: US20090215181A1 Published: 27/Aug/2009Title: Multi-Analyte Reference Solutions
Applicant/Assignee: INSTRUMENTATION LABORATORY COMPANY
Application No.: 12/203486 Filing Date: 03/Sep/2008
Abstract:The present invention provides a reference solution for use in instruments that determine hematocrit levels in biological samples by measuring the resistance and/or conductivity of the biological samples. A reference solution according to the invention achieves conductivities representative of known hematocrit levels in blood, while maintaining tolerable levels of interference with the measurement of other analytes in the reference solution.
Priority: US2003-733871 Applic. Date: 2003-12-11; US20020432373P Applic. Date: 2002-12-11
Inventor: CONLON DENNIS ROBERT [US]; MANSOURI SOHRAB [US]; VAGO GIANNANTONIO [IT]
Application No.: US20090216246A1 Published: 27/Aug/2009Title: ULTRASOUND CATHETER DEVICES AND METHODS
Applicant/Assignee: FLOWCARDIA, INC
Application No.: 12/428183 Filing Date: 22/Apr/2009
Abstract:Ultrasound catheter devices and methods provide enhanced disruption of blood vessel obstructions. Generally, an ultrasound catheter device includes an elongate flexible catheter body with one or more lumens, an ultrasound transmission member extending longitudinally through the catheter body lumen and a distal head coupled with the transmission member and positioned adjacent the distal end of the catheter body for disrupting occlusions. A proximal housing of the catheter device may include one or more features for dissipating heat from the ultrasound transmission wire, such as a fluid inlet aperture for passage of fluid, use of heat conductive materials in the proximal housing, surface features to increase the housing's surface area, heat conductive members disposed adjacent the transmission member and the like. Various irrigation fluids may be used, such as cooled, oxygen supersaturated or lubricious fluids.
Priority: US2004-927966 Applic. Date: 2004-08-26
Inventor: NITA HENRY [US]; SARGE JEFF [US]; SPANO RICHARD [US]
Application No.: US20090216317A1 Published: 27/Aug/2009Title: Delivery of Highly Lipophilic Agents Via Medical Devices
Applicant/Assignee:
Application No.: 11/886815 Filing Date: 22/Mar/2006
Abstract:An apparatus and system for delivering a lipophilic agent associated with a medical device including: a medical device, a first lipophilic agent capable of penetrating a body lumen, wherein the transfer coefficients of the first lipophilic agent is by an amount that is statistically significant of at least approximately 5,000, wherein the first lipophilic agent is associated with the medical device, wherein the first lipophilic agent/medical device is placed adjacent to said body lumen, and wherein a therapeutically effective amount of the first lipophilic agent is delivered to a desired area within a subject. Furthermore, the invention relates to a method for improving patency in a subject involving placement of a medical device in a body lumen for treating and/or preventing adjacent diseases or maintaining patency of the body lumen.
Priority: US20050664328P Applic. Date: 2005-03-23; WO2006US10307 Applic. Date: 2006-03-22
Inventor: CROMACK KEITH R [US]; TONER JOHN L [US]; BURKE SANDRA E [US]; KRASULA RICHARD W [US]; SCHWARTZ LEWIS B [US]
Application No.: US20090220482A1 Published: 03/Sep/2009Title: METHODS AND COMPOSITIONS FOR DELIVERING INTERLEUKIN-1 RECEPTOR ANTAGONIST
Applicant/Assignee: BIOMET BIOLOGICS, LLC
Application No.: 12/394723 Filing Date: 27/Feb/2009
Abstract:Methods and compositions generating and using an interleukin-1 receptor antagonist (IL-1ra)-rich solution. Methods for generating and isolating interleukin-1 receptor antagonist include incubating a liquid volume of white blood cells and platelets with polyacrylamide beads to produce interleukin-1 receptor antagonist. The interleukin-1 receptor antagonist is isolated from the polyacrylamide beads to obtain the solution rich in interleukin-1 receptor antagonist. Methods for treating a site of inflammation in a patient include administering to the site of inflammation the solution rich in interleukin-1 receptor antagonist.
Priority: US20080031803P Applic. Date: 2008-02-27; US20080116940P Applic. Date: 2008-11-21; US20090155048P Applic. Date: 2009-02-24
Inventor: HIGGINS JOEL C [US]; WOODELL-MAY JENNIFER E [US]; HOEPPNER JACY C [US]
Application No.: US20090221570A1 Published: 03/Sep/2009Title: Uses of 2-Phenyl-Substituted Imidazotriazinone Derivatives for Treating Pulmonary Hypertension
Applicant/Assignee: BAYER HELTHCARE AG
Application No.: 11/918312 Filing Date: 27/Mar/2006
Abstract:The present invention relates to the use of PDE 5 inhibitors generally and in particular of known 2-phenyl-substituted imidazotriazinone derivatives for manufacturing medicaments for the treatment of pathological states which can be treated by raising cGMP levels in certain tissues, such as, for example, of, for example: primary pulmonary hypertension, secondary pulmonary hypertension, pulmonary arterial hypertension, portopulmonary hypertension, hepatopulmonary syndrome, pulmonary hypertension caused by medicaments (amphetamines), interstitial lung disease, pulmonary hypertension occurring with HIV, thromboembolic pulmonary hypertension, pulmonary hypertension in children and neonates, pulmonary hypertension induced by atmospheric hypoxia (altitude sickness), COPD, emphysema, chronic bronchial asthma, mucoviscidosis-related pulmonary hypertension, right heart failure, left heart failure and global failure, and which can be treated by raising cGMP levels in certain tissues, such as, for example, isolated systiolic hypertension (ISH) and hardening of blood vessels, specifically of arterial blood vessels, and combination of PDE 5 inhibitors generally and in particular of known 2-phenyl-substituted imidazotriazinone derivatives with further therapeutic agents in the said indications.
Priority: DE200510016345 Applic. Date: 2005-04-09; WO2006EP02774 Applic. Date: 2006-03-27
Inventor: HANING HELMUT [DE]; SERNO PETER [DE]; BISCHOFF ERWIN [DE]; ULBRICH ERNST [DE]
Application No.: US20090221948A1 Published: 03/Sep/2009Title: SYSTEM AND METHOD FOR DELIVERY OF REGIONAL CITRATE ANTICOAGULATION TO EXTRACORPOREAL BLOOD CIRCUITS
Applicant/Assignee: HENRY FORD HEALTH SYSTEM
Application No.: 12/280450 Filing Date: 22/Feb/2007
Abstract:The present invention includes a comprehensive replacement fluid system and method for the delivery of regional citrate anticoagulation (RCA) to extracorporeal blood circuits, wherein the system may include an online clearance monitor (OCM) and a circuit effluent online sensor system (OSS) for the continuous determination of patient plasma content of ultrafilterable soultes.
Priority: US20060845646P Applic. Date: 2006-09-19; US20060790882P Applic. Date: 2006-04-11; US20060791055P Applic. Date: 2006-04-11; US20060775728P Applic. Date: 2006-02-22; US20060775729P Applic. Date: 2006-02-22; WO2007US62589 Applic. Date: 2007-02-22
Inventor: SZAMOSFALVI BALAZS [US]; FRINAK STANLEY [US]; YEE JERRY [US]
Application No.: US20090225316A1 Published: 10/Sep/2009Title: Systems for Measuring Properties of a Physiological Fluid Suspension
Applicant/Assignee:
Application No.: 12/398480 Filing Date: 05/Mar/2009
Abstract:A method of evaluating a property of a physiological fluid suspension comprises measuring a value of the property of a liquid portion of the physiological fluid suspension via light scattering, and comparing the measured value with a reference value to evaluate the property of the liquid portion of the physiological fluid suspension.
Priority: US20080068354P Applic. Date: 2008-03-05
Inventor: SUKAVANESHVAR SIVAPRASAD [US]; TEITEL EDWARD R [US]; MOHAMMAD SYED F [US]
Application No.: US20090226412A1 Published: 10/Sep/2009Title: AGENT FOR REDUCTION OF BLEEDING IN CEREBROVASCULAR DISORDER
Applicant/Assignee: ONO PHARMACEUTICAL CO., LTD.,
Application No.: 11/993917 Filing Date: 23/Jun/2006
Abstract:The present invention relates to a hemorrhage reducing agent in cerebrovascular disorder containing a poly (ADP-ribose) polymerase inhibitor (PARP inhibitor). The PARP inhibitor provides an inhibitory effect of vascular endothelial cell disorder so that it may reduce hemorrhage in cerebrovascular disorder. In addition, the PARP inhibitor inhibits the hemorrhage that is concerned about in thrombolytic agent use by using together with a thrombolytic agent, and an effect of extending therapeutic time window of a thrombolytic agent may be further expected. Furthermore, the PARP inhibitor can be a safe hemorrhage reducing agent with fewer side effects because it does not affect the blood coagulation system and the fibrinolytic system.
Priority: JP20050185606 Applic. Date: 2005-06-24; WO2006JP312569 Applic. Date: 2006-06-23
Inventor: YASUHIRO TETSUYA [JP]; KITAJIMA TAKASHI [JP]; WAKAMATSU DAISUKE [JP]; KAMOSHIMA WATARU [JP]
Application No.: US20090226415A1 Published: 10/Sep/2009Title: MODIFIED TRIDEGINS, PRODUCTION AND USE THEREOF AS TRANSGLUTAMINASE INHIBITORS
Applicant/Assignee:
Application No.: 12/406745 Filing Date: 18/Mar/2009
Abstract:The invention relates to modified tridegins, polypeptides derived from SEQ ID No. 1, in which the modification is replacement of a cysteine residue and/or one of the following amino acids-Lys2, Lys7, His10, Gly12, Leu24, Tyr31, Phe34, Arg39, Ile45, Met48, Asp50, Pro55, Phe58, Asn60, Pro65, Arg66, by another amino acid and/or N- or C-terminal deletion, whereby the remaining polypeptide comprises at least the amino acid sequence DDIYQRXVXFPXLPL (SEQ ID NO.89) and/or a covalent bonding to polyethylene glycol. Said polypeptides are novel inhibitors of transglutaminases, in particular of Factor XIIIa, of the terminal enzymes in the blood coagulation cascade. The invention further relates to methods for production of said inhibitors and the use thereof as transglutaminase inhibitors.
Priority: DE20011063333 Applic. Date: 2001-12-21; DE20021058159 Applic. Date: 2002-12-12; US2005-498752 Applic. Date: 2005-02-10; WO2002EP14684 Applic. Date: 2002-12-20
Inventor: GIERSIEFEN HELMUT [DE]; STOECKEL JOHANNES [DE]; PAMP TANJA [DE]; OHLMANN MARION [DE]
Application No.: US20090227504A1 Published: 10/Sep/2009Title: Pegylated Factor VII Glycoforms
Applicant/Assignee: NOVO NORDISK A/S
Application No.: 12/371156 Filing Date: 13/Feb/2009
Abstract:The invention concerns a preparation comprising a plurality of Factor VII polypeptides or Factor VII-related polypeptides, wherein the polypeptides comprise asparagine-linked and/or serine-linked oligosaccharide chains, and wherein at least one oligosaccharide group is covalently attached to at least one polymeric group.
Priority: DK20020000964 Applic. Date: 2002-06-21; US2007-845175 Applic. Date: 2007-08-27; US2003-609701 Applic. Date: 2003-06-30; WO2003DK00420 Applic. Date: 2003-06-20; US20020394778P Applic. Date: 2002-07-01
Inventor: KLAUSEN NIELS KRISTIAN [DK]; BJORN SOREN [DK]; BEHRENS CARSTEN [DK]; GARIBAY PATRICK WILLIAM [DK]
Application No.: US20090238852A1 Published: 24/Sep/2009Title: METHODS FOR CONTROLLING INTRACELLULAR CALCIUM LEVELS ASSOCIATED WITH AN ISCHEMIC EVENT
Applicant/Assignee: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Application No.: 12/408377 Filing Date: 20/Mar/2009
Abstract:Described herein are methods for controlling the intracellular calcium concentration in a subject prior to experiencing an ischemic event, while experiencing an ischemic event, or while suffering from ischemia. The methods comprise administering an effective amount of O-desulfated heparin to the subject. The methods described herein are also useful in treating the symptoms associated with ischemic events or ischemia.
Priority: US20080038446P Applic. Date: 2008-03-21
Inventor: KENNEDY THOMAS P [US]; BARRY WILLIAM H [US]
Application No.: US20090238874A1 Published: 24/Sep/2009Title: BIOMIMETIC COMPOSITION REINFORCED BY A POLYELECTROLYTIC COMPLEX OF HYALURONIC ACID AND CHITOSAN
Applicant/Assignee: TISSUE ENGINEERING CONSULTANTS, INC
Application No.: 12/410537 Filing Date: 25/Mar/2009
Abstract:The present invention relates to a three dimensional, malleable cell culture composition and method of forming the same comprising hyaluronic acid, chitosan and a polyelectrolytic complex of hyaluronic acid and chitosan. These three components in combination constitute an initial microenvironment for support of stromal cells, and their undifferentiated mesenchymal cell progeny. The tissue engineering device and method of forming the same comprising hyaluronic acid and chitosan and the use of said device with compositions of pluripotent cells and various formulations of cell culture media for repair of tissues is disclosed.
Priority: US2004-999848 Applic. Date: 2004-11-30; US20030525965P Applic. Date: 2003-12-01
Inventor: BREKKE JOHN H [US]
Application No.: US20090239857A1 Published: 24/Sep/2009Title: TRIAMINE DERIVATIVE
Applicant/Assignee: DAIICHI SANKYO COMPANY, LIMITED
Application No.: 11/909802 Filing Date: 31/Mar/2006
Abstract:An object of the present invention is to provide a novel compound which has a potent inhibitory effect on FXa and exhibits an excellent antithrombotic effect when orally administered. The present invention provides a compound represented by the following general formula (1): wherein R1 and R2 each independently represent a hydrogen atom, a hydroxy group, an alkyl group or an alkoxy group
Q1 represents a saturated or unsaturated bicyclic or tricyclic fused hydrocarbon group which may be substituted, a saturated or unsaturated bicyclic or tricyclic fused heterocyclic group which may be substituted, or the like
Q2 represents a single bond, a straight-chained or branched alkylene group having 1 to 6 carbon atoms, a straight-chained or branched alkenylene group having 2 to 6 carbon atoms, or the like
R3 and R4 each represent an alkyl group, or the like
m and n each represent an integer from 0 to 3
Q4 represents an aryl group
and T0 and T1 each represent a carbonyl group or the like, and a medicine containing the compound.
Priority: JP20050100335 Applic. Date: 2005-03-31; WO2006JP306930 Applic. Date: 2006-03-31
Inventor: MOCHIZUKI AKIYOSHI [JP]; NAGATA TSUTOMU [JP]
Application No.: US20090246866A1 Published: 01/Oct/2009Title: READY-TO-USE WHOLE BLOOD COLLECTION VESSEL
Applicant/Assignee:
Application No.: 12/327854 Filing Date: 04/Dec/2008
Abstract:The present invention relates to a sampling tube for collecting and processing a whole blood sample. The sampling tube contains a reagent for differential hemolysis of whole blood, wherein said reagent for differential hemolysis comprises a chemical for differential hemolysis and an anti-coagulant, and wherein said sampling tube is a ready-to-use and single-use sampling tube. It also relates to the use of said sampling tube in the processing of a whole blood sample for liquid chromatography and also to the use of a blood sample processed in such sampling tube in a liquid chromatography-based analysis.
Priority: EP20060011606 Applic. Date: 2006-06-06; WO2007EP04925 Applic. Date: 2007-06-04
Inventor: NASER WERNER [DE]; DUELFFER THOMAS [DE]; HERRMANN RUPERT [DE]; KOBOLD UWE [DE]; VON DER ELTZ HERBERT [DE]
Application No.: US20090247628A1 Published: 01/Oct/2009Title: SUBSTITUTED PHENYLCYCLOHEXYLGLYCOLATES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/409420 Filing Date: 23/Mar/2009
Abstract:Disclosed herein are substituted phenylcyclohexylglycolate-based muscarinic acetylcholine receptor modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080039166P Applic. Date: 2008-03-25
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090254117A1 Published: 08/Oct/2009Title: Venous Filter with Detachable Anchors
Applicant/Assignee:
Application No.: 12/417990 Filing Date: 03/Apr/2009
Abstract:A venous filter including anchors that detach from the struts and that remain attached to the vein wall after retrieval of the other parts of the filter is described. Anchors may be detachably connected to struts of the filter via a detachably connected ridge and groove, a detachably connected clip and ridge, a friction fit, a detachable locking pin connection, or a combination thereof.
Priority: US20080123043P Applic. Date: 2008-04-03
Inventor: PAKTER ROBERT L [US]
Application No.: US20090258337A1 Published: 15/Oct/2009Title: Thawed organ or tissue or thawed cell group to be donated, transplanted, added, or administered to living body, production process thereof, supercooled solution therefor, and production apparatus of the organ or tissue
Applicant/Assignee: ELLIE CORPORATION
Application No.: 12/383582 Filing Date: 25/Mar/2009
Abstract:The present invention aims to freeze and store organs or tissues taken from human bodies or animals and after thawing, use the resulting organs or tissues, or cells taken and extracted therefrom for medical treatment. The present invention is characterized in that the organs or tissues taken from human bodies or animals are regenerated through the steps of freezing, storing and thawing
the cells taken from the organs or tissues undergo cell division and colonization.
Priority: JP20080098782 Applic. Date: 2008-04-04
Inventor: YAGI SHUNICHI [JP]
Application No.: US20090259162A1 Published: 15/Oct/2009Title: System and Method for Plasma Reduced Platelet Collection
Applicant/Assignee:
Application No.: 12/102486 Filing Date: 14/Apr/2008
Abstract:A method and apparatus for collecting plasma reduced platelets potentially suspended in a synthetic solution from a donor. Whole blood is drawn from the donor and introduced into a separation chamber. Platelets are extracted from the separation chamber into a container, using, for example, surge (with anticoagulated plasma or a synthetic solution) or push methodologies. The remaining blood components in the separation chamber are returned back to the donor. The steps of drawing whole blood and introducing the whole blood into the separation chamber, extracting platelets from the separation chamber into the container, and returning the remaining components in the chamber back to the donor are repeated. The sequestered platelets in the container are reintroduced into the separation chamber, whereupon a plasma reduced platelet product is extracted.
Priority:
Inventor: OHASHI TOSHIYASU [JP]; PAGES ETIENNE [FR]; UHLMANN DOMINIQUE [US]; MAILLARD PASCAL [CH]; RAGUSA MICHAEL [US]
Application No.: US20090259163A1 Published: 15/Oct/2009Title: Three-Line Apheresis System and Method
Applicant/Assignee:
Application No.: 12/102407 Filing Date: 14/Apr/2008
Abstract:A blood processing system for collecting and exchanging blood components includes a venous-access device for drawing whole blood from a subject and returning blood components to the subject. The system may also include three lines connecting the venous access device to a blood component separation device and an anticoagulant source. A blood draw line fluidly connects to the venous-access device to the blood component separation device. An anticoagulant line connected to an anticoagulant source, introduces anticoagulant into the drawn whole blood. A return line, fluidly connected to the venous-access device and the blood component separation device, and returns uncollected blood component to the subject. A draw pump, an anticoagulant pump, and a return pump, respectively control the flows through the draw line, anticoagulant line, and the return line. The blood component separation device separates the drawn blood into a first blood component and a second blood component. The blood component separation device also may be configured to send the first blood component to a first blood component bag.
Priority:
Inventor: PAGES ETIENNE [FR]; RAGUSA MICHAEL [US]
Application No.: US20090259164A1 Published: 15/Oct/2009Title: System and Method for Optimized Apheresis Draw and Return
Applicant/Assignee:
Application No.: 12/102427 Filing Date: 14/Apr/2008
Abstract:A blood processing device for collecting and exchanging blood components includes a venous-access device for drawing whole blood from a subject and returning unused blood components to the subject. The system may also include a blood component separation device that separates the drawn whole blood into a first blood component and a second blood component. The blood component separation device may also be configured to send the second blood component to a second blood component storage container. The system may use a return line that fluidly connects the venous-access device and the blood component separation device to return the first blood component to the subject. The system may also have a first and second pressure sensor located on the return line. The first pressure sensor may be located between the blood component separation device and the venous-access device and may determine a first pressure within the return line. The second pressure sensor may be located on the return line between the first pressure sensor and the venous-access device and may determine a second pressure within the return line. A pump connected to the return line may control the return flow rate within the return line based on a subject access pressure determined based on the first pressure and the second pressure.
Priority:
Inventor: PAGES ETIENNE [FR]; RAGUSA MICHAEL [US]
Application No.: US20090263903A1 Published: 22/Oct/2009Title: METHOD FOR DETERMINING PROTHROMBIN TIME
Applicant/Assignee:
Application No.: 11/909208 Filing Date: 20/Mar/2006
Abstract:The present invention relates to tests for monitoring oral anticoagulation therapy and hepatocellular carcinoma (HCC). Particularly, the invention provides a method for determining prothrombin time of a plasma or whole blood sample taking account the effect which protein induced by vitamin K absence or antagonists (Pivka) has on clotting time and INR result. The primary object of the invention is to harmonise prothrombin time methods for international normalized ratio (INR) results and measure INRpivka.
Priority: FI20050000298 Applic. Date: 2005-03-21; WO2006FI50104 Applic. Date: 2006-03-20
Inventor: HORSTI JUHA [FI]
Application No.: US20090265182A1 Published: 22/Oct/2009Title: Method and system for point-of-dispensing management of anticoagulation agent therapy
Applicant/Assignee:
Application No.: 12/081794 Filing Date: 22/Apr/2008
Abstract:A method and system for point-of-dispensing, point-of-sale, or retail pharmacy management of an anticoagulation agent therapy for a subject, includes reviewing an anticoagulation regimen and obtaining data for a subject relating to anticoagulation therapy, determining an International Normalized Ratio (INR) level for the subject, determining any potential interaction of the anticoagulation agent with one or more non-anticoagulation agents that the subject intends to take or is taking, evaluating in real time any need to adjust the anticoagulation regimen, and adjusting in real time, if needed, the anticoagulation regimen based on one or both INR level and any interaction determinations, to maintain the subject's INR level within a desired range.
Priority:
Inventor: PETERSON BRENT W [US]; DAY ALLEN M [US]; NUNN CHARLES E [US]
Application No.: US20090269325A1 Published: 29/Oct/2009Title: Methods for treating bleeding disorders using sulfated polysaccharides
Applicant/Assignee: BAXTER INTERNATIONAL INC BAXTER HEALTHCARE S.A BAXTER HEALTHCARE S. A
Application No.: 12/386026 Filing Date: 13/Apr/2009
Abstract:Methods for treating bleeding disorders using non-anticoagulant sulfated polysaccharides (NASPs) as procoagulants are disclosed. NASPs can be administered as single agents, or in combination with one another, or with other medications (such as factors VII, VIII and IX) to promote hemostasis. In particular, the use of NASPs in treatment of bleeding disorders, including congenital coagulation disorders, acquired coagulation disorders, and trauma induced hemorrhagic conditions is described.
Priority: US2005-140504 Applic. Date: 2005-05-27; US20040574845P Applic. Date: 2004-05-27
Inventor: JOHNSON KIRK W [US]
Application No.: US20090269418A1 Published: 29/Oct/2009Title: Compositions and Methods for Inducing Hair Growth
Applicant/Assignee: BIOMAS LTD
Application No.: 11/662743 Filing Date: 15/Sep/2005
Abstract:Novel therapeutic methods and pharmaceutical compositions utilizing tellurium-containing compounds for inducing hair growth for the treatment of various types of alopecia and other conditions associated with hair loss.
Priority: US20040610660P Applic. Date: 2004-09-17; WO2005IL00991 Applic. Date: 2005-09-15
Inventor: ALBECK MICHAEL [IL]; SREDNI BENJAMIN [IL]
Application No.: US20090270332A1 Published: 29/Oct/2009Title: GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS, METHODS OF DETECTION AND USES THEREOF
Applicant/Assignee: CELERA CORPORATION
Application No.: 12/403552 Filing Date: 13/Mar/2009
Abstract:The present invention is based on the discovery of genetic polymorphisms that are associated with venous thrombosis. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.
Priority: US20080069687P Applic. Date: 2008-03-13
Inventor: BARE LANCE [US]; DEVLIN JAMES J [US]; ROSENDAAL FRITS R [NL]; REITSMA PIETER H [NL]; BEZEMER IRENE D [NL]
Application No.: US20090270469A1 Published: 29/Oct/2009Title: SUBSTITUTED OXAZOLIDINONES
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/428275 Filing Date: 22/Apr/2009
Abstract:The present invention relates to new oxazolidinone modulators of skeletal muscle function and tone, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080048028P Applic. Date: 2008-04-25
Inventor: GANT THOMAS G [US]; SARSHAR SEPEHR [US]
Application No.: US20090276039A1 Published: 05/Nov/2009Title: Implantable Prosthetic Valve
Applicant/Assignee: CLINASYS LLC
Application No.: 12/158747 Filing Date: 22/Dec/2006
Abstract:An implantable prosthetic valve for regulating fluid flow through a body vessel is provided. The prosthetic valve comprises an anchoring member, at least one leaflet, and a restraining member capable of temporarily preventing substantial movement of the leaflet between and open and closed position so as to allow fluid flow in the antegrade and retrograde directions. In various embodiments, the prosthetic valve reduces the risk of thrombosis. In various embodiments, the prosthetic valve reduces the appearance of potentially thrombogenic abnormal flow patterns at the site of implantation immediately following the implantation, allows cell deposition making the valve more biocompatible, less thrombogenic before flow changes resulting from valving action set in and allows tissue growth so that a partially or completely biological functioning valve may form on the scaffold provided by the implant.
Priority: US20050753716P Applic. Date: 2005-12-23; WO2006US48799 Applic. Date: 2006-12-22
Inventor: MERETEI ATTILA [US]
Application No.: US20090280570A1 Published: 12/Nov/2009Title: METHOD FOR TESTING EFFICACY OF ANTITHROMBOTIC AGENT
Applicant/Assignee:
Application No.: 11/915273 Filing Date: 08/Nov/2005
Abstract:The present invention provides a method for testing quickly and easily the manner in which an antithrombotic agent inhibits the acceleration of blood coagulation when a platelet agonist causes acceleration of blood coagulation. The invention is a test method wherein a system in which an anticoagulant is added to a portion of blood sampled from a patient being administered an antithrombotic agent (X system blood), and a system in which an anticoagulant and adenosine diphosphate or collagen are added to a portion of the abovementioned blood (Y system blood) are simultaneously measured by thromboelastograph
and the efficacy of the antithrombotic agent is assessed by comparing the R values of the X system blood and the Y system blood. If the R value of the Y system blood is not found to differ significantly from the R value of the X system blood, the drug is judged to be working. Adenosine diphosphate and collagen can be used as the anticoagulant. The present invention provides a heretofore unknown method for easily assessing the efficacy of an antithrombotic agent.
Priority: JP20050149183 Applic. Date: 2005-05-23; WO2005JP20421 Applic. Date: 2005-11-08
Inventor: KAWASAKI JUN [JP]; TANAKA KENICHI [JP]
Application No.: US20090281455A1 Published: 12/Nov/2009Title: BLOOD TEST APPARATUS
Applicant/Assignee: MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD
Application No.: 12/159904 Filing Date: 28/Dec/2006
Abstract:A blood test apparatus wherein a blood collection needle and a blood sensor can be easily attached and detached so that a burden or pain of a patient can be relieved. More specifically speaking, a blood test apparatus wherein a holder, a lancet, a blood collection needle and a blood sensor are united together as a blood sampling cartridge that is detachably mounted to the apparatus body. When this blood sampling cartridge is attached, a plunger involved in the apparatus body holds the lancet and connectors involved in the apparatus body come into contact with the blood sensor. It is preferable that the contact points with the blood sensor of the individual connectors are located at intervals at the same angle centering on a definite point.
Priority: JP20060000354 Applic. Date: 2006-01-05; JP20060000355 Applic. Date: 2006-01-05; JP20060000356 Applic. Date: 2006-01-05; JP20060000357 Applic. Date: 2006-01-05; JP20060000358 Applic. Date: 2006-01-05; JP20060022040 Applic. Date: 2006-01-31; WO2006JP326262 Applic. Date: 2006-12-28
Inventor: FUJIWARA MASAKI [JP]; AKIYAMA TOSHIHIRO [JP]; AMANO YOSHINORI [JP]
Application No.: US20090281516A1 Published: 12/Nov/2009Title: MULTILAYER CONTAINERS
Applicant/Assignee: BECTON, DICKINSON AND COMPANY
Application No.: 12/270399 Filing Date: 13/Nov/2008
Abstract:A multilayer evacuated blood collection tube is provided having a first tube layer, and a second tube layer formed on the first tube layer and a closure, the second tube layer being a nanocomposite barrier layer. Such containers include but are not limited to blood collection tubes, evacuated blood collection tubes, centrifuge tubes, culture bottles, and syringe barrels.
Priority: US2004-480540 Applic. Date: 2004-07-02
Inventor: AHERN BRIAN F [US]; GRIPPI NICHOLAS A [US]; SOSKEY PAUL R [US]; CARANO DONALD J [US]; HUTTON NORMAN J [US]; DESALVO DANIELLE M [US]; LUSARDI GREGORY L [US]
Application No.: US20090285722A1 Published: 19/Nov/2009Title: Collection container assembly with nanocomposite barrier coating
Applicant/Assignee:
Application No.: 12/383058 Filing Date: 19/Mar/2009
Abstract:An evacuated container assembly suitable for use in connection with blood collection including: (a) a container member formed of a first polymeric material and having a sidewall and one or more openings
(b) a nanocomposite barrier coating disposed on the container member having a thickness of up to about 30 microns and being derived from an aqueous dispersion including (i) a dispersed barrier matrix polymer
and (ii) a substantially exfoliated silicate filler having an aspect ratio of more than 50
and (c) one or more sealing members disposed in the opening(s) operative to hermetically seal the cavity
wherein the cavity is evacuated and maintains a pressure below atmospheric pressure and exhibits a draw volume loss lower than that of a like assembly without a nanocomposite barrier film by a factor of at least 1.5.
Priority: US20080070128P Applic. Date: 2008-03-20
Inventor: SOSKEY PAUL R [US]; PARMER JR JEROME F [US]; GOLDBERG HARRIS A [US]; KARIM DOUGLAS P [US]; SAMANTARA LAXMI [US]; FEENEY CARRIE A [US]; FARRELL MICHELE [US]
Application No.: US20090285786A1 Published: 19/Nov/2009Title: METHOD TO MODULATE HEMATOPOIETIC STEM CELL GROWTH
Applicant/Assignee: CHILDREN'S MEDICAL CENTER CORPORATION
Application No.: 12/294344 Filing Date: 26/Mar/2007
Abstract:The present invention provides for compositions and methods for modulating hematopoietic stem cell populations by using HCS modulators, which are agents that either increase HSC numbers or decrease HSC numbers as desired by a particular indication. For example, HSC modulators found to increase HSC numbers include prostaglandin E2 (PGE2) and agents that stimulate the PGE2 pathway. Conversely, HSC modulators that prevent PGE2 synthesis decrease HSC numbers. HCS modulators may be used in vitro, in vivo, or ex vivo.
Priority: US20060785968P Applic. Date: 2006-03-24; WO2007US07419 Applic. Date: 2007-03-26
Inventor: ZON LEONARD I [US]; NORTH TRISTA E [US]; GOESSLING WOLFRAM [US]
Application No.: US20090285811A1 Published: 19/Nov/2009Title: ANTI-INFLAMMATORY AND IMMUNOSUPPRESSIVE GLUCOCORTICOID STEROIDS
Applicant/Assignee: AUSPEX PHARMACEUTICALS, INC
Application No.: 12/464150 Filing Date: 12/May/2009
Abstract:The present invention relates to new glucocorticoid steroid modulators of glucocorticoid receptor, pharmaceutical compositions thereof, and methods of use thereof.
Priority: US20080052872P Applic. Date: 2008-05-13
Inventor: GANT THOMAS G [US]; SHAHBAZ MANOUCHER M [US]; MEJORADO LUPE [US]
Application No.: US20090285892A1 Published: 19/Nov/2009Title: METHODS AND SYSTEMS FOR EXPANDING AC133+ CELLS AND DIRECTING DIFFERENTIATION
Applicant/Assignee:
Application No.: 12/351630 Filing Date: 09/Jan/2009
Abstract:The invention provides, among other things, methods and systems for expanding CD133+ cells. The invention further provides methods and systems for increasing the blood flow to an ischemic tissue in a subject in need thereof, such as to ischemic myocardium. The invention further provides methods and systems for directing differentiation of expanded CD133+ cells. The invention further provides methods and systems for treating a subject with differentiated cells in a subject in need thereof.
Priority: US2007-975492 Applic. Date: 2007-10-18; US20060852598P Applic. Date: 2006-10-18; US20080010917P Applic. Date: 2008-01-10; US20080190544P Applic. Date: 2008-08-28
Inventor: SAKTHIVEL RAMASAMY [US]; BROWN DONALD J [US]; MAO HAI-QUAN [US]; DOUAY LUC [FR]; POMPILI VINCENT J [US]; MCLNTOSH KEVIN [US]; DAS HIRANMOY [US]; ZHAO YUKANG [US]
Application No.: US20090286251A1 Published: 19/Nov/2009Title: Enzyme Reagents for Amplification of Polynucleotides in the Presence of Inhibitors
Applicant/Assignee: NEW ENGLAND BIOLABS, INC
Application No.: 12/466856 Filing Date: 15/May/2009
Abstract:Compositions and methods are provided for amplifying polynucletoides from samples containing inhibitors that normally inhibit amplification using an enzyme blend containing a plurality of polymerases. The ability to amplify polynucleotides efficiently in the presence of inhibitors allows the enzyme reagent to be used in both routine amplification and real-time amplification from inhibitor-containing samples.
Priority: US20080053740P Applic. Date: 2008-05-16
Inventor: XU YAN [US]
Application No.: US20090287305A1 Published: 19/Nov/2009Title: Wholly implantable non-natural heart for humans
Applicant/Assignee:
Application No.: 12/152896 Filing Date: 19/May/2008
Abstract:A wholly implantable non-natural heart for humans is a double pump configuration provided with two auricles and two ventricles. Both the said auricles and ventricles are driven by solenoid actuators interacting with high energy magnets
the auricles and ventricles which are hollow chambers are provided with one-way valves in the usual manner, for the purpose of effectively and rhythmically moving blood to and from the said chambers
power generation for driving said solenoid actuators, as well as an electronic control unit is accomplished by a power generating module which could be a simple battery, a miniature spring-driven generator, a mems generator or a redundant self-sustaining generator or a combination of all of the above
the self-sustaining generator has been proposed and designed to power this present artificial heart and will be presented in a separate patent application in the near future as a follow up to this present one
the aforementioned electronic control unit is preferably configured to amplify the signals from the power generating unit as well as utilizing input/output signals from temperature and pressure sensors embedded in the heart to vary contractile force and frequency of beats, based on bodily requirements, thereby mimicking some functions of the natural heart
the electronic unit is also preferably provided with a translator chip that converts signals from the cardiac/vargus trunks (sympathetic and parasympathetic nerves) via electrodes into clear electric currents for varying actuator outputs
the heart would be implanted in the normal position in the chest, atop the diaphragm, while the electronic control unit and the power generation module would preferably be implanted behind the breastbone and lower abdomen respectively
all components of the present invention are amenable to current mass production techniques and miniaturization for the purpose of fitting into individuals of various sizes
as is clearly shown in FIG. 1, this present invention is an integral three-tiered configuration constituted of pumping unit I, the power generating unit II and the controller III. Also, as aforementioned, additional signals from the embedded temperature and pressure sensors, as well as nerve connecting electrodes are used to manipulate instantaneous outputs. The said electrodes are in the form of cuffs and are to be implanted on the vargus nerves (sympathetic and parasympathetic)
Texas Instruments (TI) manufactures reliable operational and instrumentation amplifiers which can detect condition, and amplify nerve signals. The VCO in the controller uses the signals to manipulate instantaneous outputs of the actuating solenoids.
Priority:
Inventor: AMALAHA LEONARD D [US]
Application No.: US20090288178A1 Published: 19/Nov/2009Title: INSECT CELL LINE FOR PRODUCTION OF RECOMBINANT GLYCOPROTEINS WITH SULFATED COMPLEX N-GLYCANS
Applicant/Assignee:
Application No.: 12/421977 Filing Date: 10/Apr/2009
Abstract:A transgenic insect cell line for production of recombinant glycoproteins possessing sulfated, complex N-glycans is provided.
Priority: WO2007US80997 Applic. Date: 2007-10-10; US20060850573P Applic. Date: 2006-10-10
Inventor: JARVIS DONALD L [US]
Application No.: US20090297596A1 Published: 03/Dec/2009Title: Nanoparticulate and Controlled Release Compositions Comprising a Platelet Aggregation Inhibitor
Applicant/Assignee: ELAN PHARMA INTERNATIONAL LIMITED
Application No.: 11/568835 Filing Date: 23/May/2006
Abstract:The present invention provides a composition comprising a platelet aggregation inhibitor, for example, cilostazol, or a salt or derivative thereof, useful in the treatment and prevention of ischemic symptoms. The invention provides a composition which comprises nanoparticulate particles comprising the platelet aggregation inhibitor and at least one surface stabilizer. The nanoparticulate particles have an effective average particle size of less than about 2000 nm. The invention provides also a composition that delivers a platelet aggregation inhibitor, or nanoparticles comprising the same, in a pulsatile or continuous manner.
Priority: US20050683620P Applic. Date: 2005-05-23; WO2006US19905 Applic. Date: 2006-05-23
Inventor: DEVANE JOHN [IE]; STARK PAUL [IE]; FANNING NIALL [IE]; REKHI GURVINDER [US]; JENKINS SCOTT [US]; LIVERSIDGE GARY [US]
Application No.: US20090298060A1 Published: 03/Dec/2009Title: METHODS FOR DIAGNOSING AND MONITORING THE STATUS OF SYSTEMIC LUPUS ERYTHEMATOSUS
Applicant/Assignee: XDX, INC
Application No.: 11/938227 Filing Date: 09/Nov/2007
Abstract: and diagnosing or monitoring the status of SLE in the subject or patient by applying at least one statistical method to the expression of the genes of the diagnostic set.
Priority: US20060858147P Applic. Date: 2006-11-09
Inventor: LAL PREETI G [US]; WILLIAMS GAVIN E [US]; FRY KIRK E [US]; SUN JINGTAO [US]; DEDRICK RUSSELL L [US]
Application No.: US20090298078A1 Published: 03/Dec/2009Title: METHOD FOR THE DETECTION OF AN ACTIVATION OF THE IMMUNE SYSTEM OR THE EXTENT OF CELL DEATH
Applicant/Assignee: LEUKOCARE AG
Application No.: 12/442383 Filing Date: 01/Oct/2007
Abstract:The present invention relates to a method for the detection of an activation of the immune system, preferably in the sense of an NET formation, or the extent of cell death in a non-tumorous tissue or in a body fluid, wherein free DNA is measured in a sample from an individual. Furthermore, the invention relates to a method for the production of a kit for the detection of an activation of the immune system or the extent of cell death in an individual, comprising the packaging of a fluorescent dye and a DNA standard in at least one container.
Priority: US20060827571P Applic. Date: 2006-09-29; WO2007EP08523 Applic. Date: 2007-10-01
Inventor: MARGRAF STEFAN [DE]
Application No.: US20090298090A1 Published: 03/Dec/2009Title: METHODS TO MEASURE IMMUNOSUPPRESSIVE TACROLIMUS, SIROLIMUS, AND CYCLOSPORIN A COMPLEXES IN A BLOOD SAMPLE
Applicant/Assignee: ABBOTT LABORATORIES
Application No.: 12/539825 Filing Date: 12/Aug/2009
Abstract:The present invention provides methods, diagnostic assays, and diagnostic kits based on said methods, to determine levels of immunosuppressive complexes containing immunosuppressive drugs tacrolimus, sirolimus and cyclosporine A separately and in combination, formed in the blood of a drug-treated patient or in a patient candidate to immunosuppressive drug therapy. These methods, assays and kits are especially useful when using automated systems.
Priority: US2006-398997 Applic. Date: 2006-04-06; US20050668714P Applic. Date: 2005-04-06
Inventor: DRENGLER SUSAN M [US]; BAUGHER BENNETT W [US]
Application No.: US20090298103A1 Published: 03/Dec/2009Title: Predicting hemostatic risk
Applicant/Assignee: THE UNIVERSITY OF VERMONT AND STATE AGRICULTURE COLLEGE
Application No.: 12/454677 Filing Date: 20/May/2009
Abstract:Featured are methods for assessing hemostatic risk including the risk for ACS. Such methods include acquiring blood/plasma composition based on a biological sample obtained from a subject, determining parameters associated with blood clotting, simulating in silico blood clotting using the determined parameters and comparing the results of such simulation to a reference and to determine the hemostatic risk from said comparing. In further embodiments, such methods further include selecting a treatment regime or protocol based on the results of such comparing. In yet further embodiments, such methods further include assessing the efficacy of medicants, drugs and the like of a given treatment protocol such as by simulating in silico the application of such medicants, drugs and the like.
Priority: US20080054503P Applic. Date: 2008-05-20
Inventor: MANN KENNETH G [US]; ZIEDINS KATHLEEN B [US]; ORFEO THOMAS [US]; HOCKIN MATTHEW F [US]; EVERSE STEPHEN J [US]
Application No.: US20090299223A1 Published: 03/Dec/2009Title: BLOOD COMPONENT COLLECTION APPARATUS AND METHOD
Applicant/Assignee: TERUMO KABUSHIKI KAISHA
Application No.: 12/488649 Filing Date: 22/Jun/2009
Abstract:A blood component collection apparatus comprises a blood component collecting circuit which includes an anticoagulant line for feeding an anticoagulant and a line for collecting an initial flow of collected blood. In the blood component collection apparatus, air is intermediately present between the anticoagulant and the blood in the passage of a blood collection needle side line, after a priming operation is performed in which anticoagulant is supplied from the anticoagulant line toward the side of a centrifugal separator in the blood collection needle side line through a branch connector and after an initial flow collecting operation is performed in which the initial flow of blood is collected.
Priority: JP20050178316 Applic. Date: 2005-06-17; US2006-453840 Applic. Date: 2006-06-16
Inventor: HIRABUKI MAKOTO [JP]
Application No.: US20090304577A1 Published: 10/Dec/2009Title: Peptides for Treatment and Diagnosis of Autoimmune Disease
Applicant/Assignee:
Application No.: 11/990281 Filing Date: 09/Aug/2006
Abstract:There are provided peptides derived from antibodies with reactivity against a GPI linkage epitope and functionally equivalent ligands. These peptides can be used in the therapy and diagnosis of a variety of diseases, all of which are considered to be caused by the inappropriate presence in the body of autoantibodies which are reactive with GPI linkage epitopes. There is also described a mechanism of action of these autoantibodies which compromises the organism, so causing disease, and a method of prevention of disease and detection of the autoantibody.
Priority: GB20050016527 Applic. Date: 2005-08-11; GB20060009920 Applic. Date: 2006-05-18; GB20060009921 Applic. Date: 2006-05-18; WO2006GB02977 Applic. Date: 2006-08-09
Inventor: MATOSSIAN-ROGERS ARPI [GB]
Application No.: US20090305315A1 Published: 10/Dec/2009Title: HUBBED DUAL CANNULA DEVICE FOR CLOSED CONTAINER SAMPLING SYSTEMS
Applicant/Assignee:
Application No.: 12/480476 Filing Date: 08/Jun/2009
Abstract:The present invention provides a hubbed dual cannula device for extracting a fluid sample from a closed container. The device comprises a housing hub, two substantially parallel needles, a venting valve and a hydrophobic membrane, and may be used effectively to extract a fluid sample from a sealed container, such as a vacuum tube, without damaging the cellular components or activating platelets in the fluid sample. Also provided are methods for using the disclosed device to extract a fluid sample from a closed container and kits for measuring platelet aggregation using such a device.
Priority: US20080060076P Applic. Date: 2008-06-09
Inventor: GANDOLA KENT RAPHAEL [US]; KAPLAN DAVID ELLIOTT [US]; BARE REX O [US]; JOHNSON CHRISTOPHER JOHANN [US]
Application No.: US20090305325A1 Published: 10/Dec/2009Title: Method for Preservation of Human Hematopoietic Stem or Progenitor Cells
Applicant/Assignee: DEPARTMENT OF BIOTECHNOLOGY NATIONAL CENTRE FOR CELL SCIENCE INDIAN INSTITUTE OF SCIENCES
Application No.: 12/096292 Filing Date: 27/Jun/2006
Abstract:Maintenance of quiescent hematopoietic stem and progenitor cells (HSPC) in culture without the addition of exogenous growth factors is an important aspect in clinical hematology. A recent report described the ability of Flt3 receptor-interacting lectin (FRIL) in the maintenance of cord blood (CB) derived progenitors in vitro. Since FRIL is a mannose binding lectin, the effectiveness of four such lectins of well-characterized specificities on the preservation of HSPC of CB origin have been examined. The HSPC preservation activity of lectins was assessed by in vitro colony forming unit (CFU) and long-term culture initiating cell (LTC-IC) assays. It was found that all four lectins had a HSPC preservation activity at least up to 30 days in culture without addition of exogenous growth factors. The results indicate that use of such lectins may provide a cost effective method of HSPC maintenance for clinical use.
Priority: IN2005DE03284 Applic. Date: 2005-12-06; WO2006IN00215 Applic. Date: 2006-06-27
Inventor: KALE VAIJAYANTI P [IN]; LIMAYE LALITA S [IN]; HINGE ASHWINI [IN]; SUROLIA AVADHESHA [IN]
Application No.: US20090305407A1 Published: 10/Dec/2009Title: Devices and Methods for Sampling Biological Fluids
Applicant/Assignee:
Application No.: 12/406815 Filing Date: 18/Mar/2009
Abstract:Devices, instruments, systems and methods are provided in which a primary line that receives a biological fluid is selectively sampled by a plurality of collection chambers. Selective sampling occurs by selectively accessing the primary line and selective engagement of a sampling pump under control of a microprocessor. Further, the instrument housing reversibly houses a drive assembly and sample collection housing to permit the interchangeability of drive assemblies and collection housings and thus enhance sterility or reduction of cost.
Priority: US20080037587P Applic. Date: 2008-03-18
Inventor: TEMPLE JOHN [US]
Application No.: US20090306623A1 Published: 10/Dec/2009Title: Multiple ratio fluid dispenser
Applicant/Assignee: ARTERIOCYTE MEDICAL SYSTEMS, INC
Application No.: 12/462885 Filing Date: 10/Aug/2009
Abstract:A double syringe delivery system is disclosed for holding a pair of syringes in a manner so as to accommodate the simultaneous activation of the plunger of each syringe in order to effect simultaneous delivery of the contents of each syringe. The delivery system includes a delivery mechanism for delivering the contents of both syringes to a site of application. The delivery system further includes a support member that is positioned between the two syringe bodies. The elongated support member has resilient, C-shaped clamps on one end of the support member. The clamps are designed to be removably clamped onto the applicator so that the syringe barrels will be held together in a parallel manner. The elongated support member further comprises finger grips. A plunger connects the two syringe plungers so that they can also be simultaneously activated.
Priority: US2004-876147 Applic. Date: 2004-06-24; US2002-212430 Applic. Date: 2002-08-05; US20020388822P Applic. Date: 2002-06-14
Inventor: MCINTOSH KEVIN D [US]; ALBRECHT RICHARD M [US]
Application No.: US20090307179A1 Published: 10/Dec/2009Title: Genetic analysis
Applicant/Assignee:
Application No.: 12/383110 Filing Date: 18/Mar/2009
Abstract:The present invention provides methods for generating genetic profiles or analyses. Included are methods for conducting comprehensive, dynamic genetic analysis. Also provided are methods for determining genetic health scores for specific phenotypes, such as diseases, disorders, traits, and conditions, as well as for organ systems, for certain medical specialties, and for overall health.
Priority: US20080037959P Applic. Date: 2008-03-19; US20080050126P Applic. Date: 2008-05-02; US20080091342P Applic. Date: 2008-08-22; US20080136266P Applic. Date: 2008-08-22; US20080198765P Applic. Date: 2008-11-07
Inventor: COLBY BRANDON [US]; SLATER BATHANY [US]; COLBY MELVYN [US]; COLBY BRYON [US]
Application No.: US20090307180A1 Published: 10/Dec/2009Title: Genetic analysis
Applicant/Assignee:
Application No.: 12/383117 Filing Date: 18/Mar/2009
Abstract:The present invention provides methods for generating genetic profiles or analyses. Included are methods for conducting comprehensive, dynamic genetic analysis. Also provided are methods for determining genetic health scores for specific phenotypes, such as diseases, disorders, traits, and conditions, as well as for organ systems, for certain medical specialties, and for overall health.
Priority: US20080037959P Applic. Date: 2008-03-19; US20080050126P Applic. Date: 2008-05-02; US20080091342P Applic. Date: 2008-08-22; US20080136266P Applic. Date: 2008-08-22; US20080198765P Applic. Date: 2008-11-07
Inventor: COLBY BRANDON [US]; SLATER BETHANY [US]; COLBY MELVYN [US]; COLBY BRYON [US]
Application No.: US20090307181A1 Published: 10/Dec/2009Title: Genetic analysis
Applicant/Assignee:
Application No.: 12/383122 Filing Date: 18/Mar/2009
Abstract:The present invention provides methods for generating genetic profiles or analyses. Included are methods for conducting comprehensive, dynamic genetic analysis. Also provided are methods for determining genetic health scores for specific phenotypes, such as diseases, disorders, traits, and conditions, as well as for organ systems, for certain medical specialties, and for overall health.
Priority: US20080037959P Applic. Date: 2008-03-19; US20080050126P Applic. Date: 2008-05-02; US20080091342P Applic. Date: 2008-08-22; US20080136266P Applic. Date: 2008-08-22; US20080198765P Applic. Date: 2008-11-07
Inventor: COLBY BRANDON [US]; SLATER BETHANY [US]; COLBY MELVYN [US]; COLBY BRYON [US]
Application No.: US20090311309A1 Published: 17/Dec/2009Title: Novel Tissue Support
Applicant/Assignee: TYCO HEALTHCARE GROUP LP
Application No.: 12/544735 Filing Date: 20/Aug/2009
Abstract:The present disclosure provides tissue supports which may be utilized by themselves or in combination with other tissue closure means to enhance wound closure and healing. The tissue supports are made of a material which shrinks upon application of heat or light to further support the tissue and/or wound to which it is applied.
Priority: US2007-825478 Applic. Date: 2007-07-06; US20060819152P Applic. Date: 2006-07-07
Inventor: PROMMERSBERGER STOPEK MEGAN [US]
Application No.: US20090311706A1 Published: 17/Dec/2009Title: QUANTITATIVE ANALYSIS OF IN VIVO MUTATION AT THE PIG-A LOCUS
Applicant/Assignee: LITRON LABORATORIES, LTD
Application No.: 12/483829 Filing Date: 12/Jun/2009
Abstract:The invention relates to methods and kits for the quantitative analysis of in vivo mutation frequencies of the Pig-A gene in individuals exposed to a genotoxicant, particularly using peripheral blood samples of vertebrates.
Priority: US20080061031P Applic. Date: 2008-06-12
Inventor: DERTINGER STEPHEN D [US]
Application No.: US20090317329A1 Published: 11/Jun/2009Title: Anticoagulation Agent and Uses Thereof
Applicant/Assignee: BAKER MEDICAL RESEARCH INSTITUTE BAKER IDI HEART & DIABETES INSTITUTE HOLDINGS LIMITED
Application No.: 11/988196 Filing Date: 05/Jul/2006
Abstract:The present invention provides an anticoagulant agent including a first element capable of inhibiting coagulation and a second element capable of targeting an activated platelet wherein upon administration of element directs the first element to the activated platelet. Also provided is a probe for detecting a blood vessel abnormality including (a) a binding element capable of targeting an activated platelet and (b) a label. Applicant has shown that agents and probes directed to activated platelets are useful in the diagnosis and therapy of coagulation disorders.
Priority: AU20050903570 Applic. Date: 2005-07-05; AU20050905522 Applic. Date: 2005-10-06; WO2006AU00943 Applic. Date: 2006-07-05
Inventor: PETER KARLHEINZ [AU]
Application No.: US20090317468A1 Published: 24/Dec/2009Title: MULTICOMPARTMENT GRANULATE FORMULATIONS FOR ACTIVE SUBSTANCES
Applicant/Assignee: BAYER TECHNOLOGY SERVICES GMBH
Application No.: 12/374568 Filing Date: 07/Jul/2007
Abstract:The invention relates to molded article that contains active substances and comprises at least two compartments that have a different material composition. Each compartment is independently provided with at least one active substance that is contained in a matrix. Each matrix encompasses at least one filler at a concentration of >=20 percent by weight to <=100 percent by weight relative to the total weight of the respective matrix. The invention further relates to a method for producing such molded articles as well as the use thereof.
Priority: DE200610033723 Applic. Date: 2006-07-21; WO2007EP06046 Applic. Date: 2007-07-07
Inventor: LETMATHE CLAUDIA [DE]; EBLE AXEL [DE]; BORK OLAF [DE]
Application No.: US20090317471A1 Published: 24/Dec/2009Title: CONTROLLED-RELEASE FORMULATIONS, METHOD OF MANUFACTURE, AND USE THEREOF
Applicant/Assignee: MUTUAL PHARMACEUTICAL COMPANY, INC
Application No.: 12/330280 Filing Date: 08/Dec/2008
Abstract:The present invention includes a controlled-release composition having a matrix. The matrix contains a pharmaceutically effective amount of an active agent or a pharmaceutically acceptable salt or solvate thereof, an ionic non-gelling matrix polymer, and a pH modifier. The ionic non-gelling matrix polymer is practically insoluble and unswellable at a first aqueous fluid pH and is soluble at a second aqueous fluid pH. The pH modifier is present in an amount to control the release of the active agent from the composition. The controlled-release composition is substantially free of a gelling or swellable excipient and does not contain a functional coating or a lipophilic component. The present invention also provides methods of making and using the controlled-release compositions.
Priority: US2008-143460 Applic. Date: 2008-06-20
Inventor: NARINGREKAR GANDHA V [US]; ARNOLD KRISTIN A [US]; ERKOBONI DAVID [US]
Application No.: US20090317473A1 Published: 24/Dec/2009Title: CONTROLLED-RELEASE FORMULATIONS, METHOD OF MANUFACTURE, AND USE THEREOF
Applicant/Assignee:
Application No.: 12/143460 Filing Date: 20/Jun/2008
Abstract:The present invention includes a controlled-release composition having a matrix. The matrix contains a pharmaceutically effective amount of an active agent or a pharmaceutically acceptable salt, solvate, ester, and/or prodrug thereof, an ionic non-gelling matrix polymer, and a pH modifier. The ionic non-gelling matrix polymer is practically insoluble and unswellable at a first aqueous fluid pH and is soluble at a second aqueous fluid pH. The pH modifier is present in an amount to control the release of the active agent from the composition. The controlled-release composition is substantially free of a gelling or swellable excipient. The present invention also provides methods of making and using the controlled-release compositions.
Priority:
Inventor: NARINGREKAR GANDHA V [US]; ARNOLD KRISTIN A [US]; ERKOBONI DAVID [US]
Application No.: US20090317790A1 Published: 24/Dec/2009Title: Method for the Production of Frozen Blood or Frozen Blood Cells for Biological Assays
Applicant/Assignee:
Application No.: 12/443302 Filing Date: 27/Sep/2007
Abstract:The present invention relates to an improved method for cryo-preservation of human whole blood containing monocytes and lymphocytes at temperatures of between -40 DEG C. and -60 DEG C., preferably at -60 DEG C., whereby the function of monocytes and lymphocytes is preserved. The present invention, particularly relates to a method for cryo-preservation of human whole blood containing monocytes and lymphocytes without the need for an isolation of peripheral blood mononuclear cells (PBMCs), or blood cells.
Priority: EP20060020256 Applic. Date: 2006-09-27; WO2007EP08439 Applic. Date: 2007-09-27
Inventor: MONTAG-LESSING THOMAS [DE]; SPREITZER INGO [DE]; LOESCHNER BETTINA [DE]
Application No.: US20090317843A1 Published: 24/Dec/2009Title: METHOD FOR MEASURING PLASMA LEVELS OF LONG PENTRAXIN PTX3
Applicant/Assignee:
Application No.: 12/520059 Filing Date: 22/Jun/2009
Abstract:The present invention relates to a method for measuring PTX3 in a biological fluid, particularly in human or animal plasma. Particularly, the present invention relates to a method for measuring PTX3 levels in a human or animal derived plasma sample, comprising a stage of the treatment of said plasma sample with a red blood cell agglutinating agent and a subsequent stage of determining the plasma levels of PTX3.
Priority: WO2006IT00872 Applic. Date: 2006-12-22
Inventor: MANTOVANI ALBERTO [IT]; PERI GIUSEPPE [IT]; PASQUALINI FABIO [IT]
Application No.: US20090326510A1 Published: 31/Dec/2009Title: Drug Delivery Methods and Systems
Applicant/Assignee:
Application No.: 12/165328 Filing Date: 30/Jun/2008
Abstract:Drug delivery methods and systems that include a determination of whether a cardiac condition is normal or abnormal, so that a drug may be administered in accordance with that determination. In one implementation, a drug delivery device may be controlled to reduce or stop the drug administration when a normal cardiac condition is detected. In another implementation, a patient monitoring device determines the duration that a cardiac condition is normal and provides an output indicative of the determination so that the patient may alter a therapy accordingly.
Priority:
Inventor: HAEFNER PAUL A [US]; MOON LOELL BOYCE [US]