Abstract: The present invention relates to a pharmaceutical composition comprising cocaethylene as active ingredient and to its use in treating dependence on psychoactive substances, in particular on cocaine.
Type:
Grant
Filed:
June 10, 2002
Date of Patent:
October 21, 2003
Assignee:
Debussy Holding SA
Inventors:
William Lowenstein, Mario Sanchez, Benedicte Lepere-Prevot, Benjamin De Rothschild
Abstract: Methods for inhibiting angiogenisis are disclosed the comprise administering oleouropein and/or the products of its hydrolysis in therapeutically effective amounts. The methods and compositions of the present invention are particularly effective in inhibiting the vascularization of endothelial cells, and may be utilized to treat a wide variety of cancers, ocular diseases, and inflammatory conditions.
Type:
Grant
Filed:
May 22, 2002
Date of Patent:
October 14, 2003
Assignee:
Antigen Biologicals Corporation
Inventors:
Hamdi K. Hamdi, Jeffrey H. Tavis, Raquel Castellon
Abstract: The present invention is directed to methods for the prevention or inhibition of angiogenesis. The method is accomplished by the administration of an effective amount of 15-epi-16-(para-fluoro)-phenoxy-lipoxin A4, LXA4, 15-epi-LXA4 or 15-R/S-methyl, LXA4 and pharmaceutically acceptable salts, esters, amides, carboxylic acids, or prodrugs thereof, to a subject in need thereof. As a consequence of the action of the therapeutic agent, angiogenesis is prevented or inhibited in the subject.
Abstract: Desensitization of receptors that control disease is prevented by inhibiting G-protein receptor kinases. This has applicability, e.g., for patients with heart failure or on a left ventricular heart device or a heart pump after surgery or about to undergo surgery and at high risk for a cardiac event or on an opiate or addicted to opiate or with cystic fibrosis or rheumatoid arthritis.
Type:
Grant
Filed:
October 25, 2002
Date of Patent:
September 30, 2003
Assignee:
Duke University
Inventors:
Jonathan S. Stamler, Robert J. Lefkowitz, Erin J. Whalen, Walter J. Koch, Claude A. Piantadosi
Abstract: A method is provided for treating a patient having a disease associated with undesirable or uncontrolled cell proliferation. The method comprises: administering to the patient an anthracycline for a period of time during which a 20(S)-camptothecin is not present in a pharmacologically active form in patient's blood; and administering a 20(S)-camptothecin to the patient.
Abstract: Interleukin (IL) antagonists are provided for the treatment in humans of neurological disorders, trauma, injuries or compression; neurodegenerative disorders including Alzheimer's Disease; demyelinating neurological disorders including multiple sclerosis; retinal disorders; and muscular disorders. The IL antagonists are used to treat these disorders by inhibiting the action of IL in the human body. The administration of these IL antagonists is performed by intrathecal administration; intracerebroventricular administration; intranasal administration; by inhalation; or by alternative routes of administration.
Abstract: The invention relates to the combined administration of PDE inhibitors and &bgr;2 adrenoceptor agonists for the treatment of respiratory tract disorders.
Abstract: The present invention provides methods and kits for improving or maintaining vascular health, including preventing myocardial infarction or stroke; maintaining or improving vascular reactivity; treating acute or chronic renal failure, peripheral arterial occlusive disease, coronary artery disease, or Raynaud's phenomenon; or lowering plasma levels of Lp(a) using an estrogen agonist/antagonist.
Type:
Grant
Filed:
October 15, 2001
Date of Patent:
September 16, 2003
Assignee:
Pfizer Inc.
Inventors:
Wesley W. Day, Andrew G. Lee, David D. Thompson
Abstract: The present invention provides methods and compositions for treating infectious disease or suppressing inflammation associated therewith or ameliorating symptoms thereof by the suppression of the activity of a member of the interleukin-1&bgr;-converting enzyme (ICE)/CED-3 family of proteases. Also provided are compositions useful for these purposes. Exemplary compounds useful in the methods of the invention are provided herein.
Type:
Grant
Filed:
November 13, 2001
Date of Patent:
August 26, 2003
Assignee:
IDUN Pharmaceuticals, Inc.
Inventors:
Lawrence C. Fritz, Kevin J. Tomaselli, Donald S. Karanewsky, Steven D. Linton, Xu Bai
Abstract: The invention is directed to pharmaceutical compositions containing small organic molecules having the ability to mimic or agonize hepatocyte growth factor/scatter factor (HGF/SF) activity, useful for promoting, for example, vascularization of tissues or organs for promoting wound or tissue healing, or augmenting or restoring blood flow to ischemic tissues such as the heart following myocardial infarction.
Type:
Grant
Filed:
December 19, 2001
Date of Patent:
August 26, 2003
Assignee:
North Shore-Long Island Jewish Research Institute
Inventors:
Sivaram Pillarisetti, Itzhak D. Goldberg
Abstract: Neurodegenerative diseases, such as dementia, including Alzheimer's disease, can be treated or prevented by administering an effective amount of triflusal or its metabolite, or a pharmaceutically acceptable salt or a prodrug thereof.
Type:
Grant
Filed:
April 4, 2002
Date of Patent:
August 26, 2003
Assignee:
J. Uriach & Cia, S.A.
Inventors:
Manuel Merlos Roca, Alberto Fernandez De Arriba, Fernando Cavalcanti De Maria, Agustà Miralles Acosta, Mariano Sanchez Crespo, Julián Garcia Rafanell, Javier Forn Dalmau
Abstract: This invention provides a method for increasing the concentration of ascorbic acid in the cells of a subject which comprises administering to the subject an amount of dehydroascorbic acid effective to increase the concentration of ascorbic acid in the subject's cells. This invention further provides a method for increasing the antioxidant potential of the cells of a subject which comprises administering to the subject an amount of dehydroascorbic acid effective to increase the antioxidant potential of the subject's cells. This invention also provides a method for increasing the concentration of ascorbic acid in brain tissue of a subject which comprises administering to the subject an amount of dehydroascorbic acid effective to increase the concentration of ascorbic acid in the subject's brain tissue.
Type:
Grant
Filed:
June 13, 2001
Date of Patent:
August 19, 2003
Assignee:
Sloan-Kettering Institute for Cancer Research
Inventors:
David B. Agus, Juan C. Vera, David W. Golde
Abstract: This invention also provides a method to inhibit neovascularization in tissue by delivering to the cell or tissue an effective amount of gossypol, or a pharmaceutically acceptable salt, derivative or prodrug thereof. Also provided herein is a method for treating a disease associated with hyproliferation of endothelial cells and/or neovascularization by administering to a subject an effective amount of gossypol, or a pharmaceutically acceptable salt, derivative or prodrug thereof. Kits to treat patients are provided as well.
Abstract: This invention relates to a method of using novel 5-(arylsulfonyl)-5-(arylsulfinyl)- and 5-(arylsulfanyl)thiazolidine-2,4-diones of Formula (I), wherein Ar, Ar′, R6, m and n are as defined in the specification as inhibitors of Ras FPTase, and may be used as an alternative to, or in conjunction with, traditional cancer therapy for treating ras- oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid
Type:
Grant
Filed:
August 23, 2002
Date of Patent:
August 12, 2003
Assignee:
Wyeth Holdings Corporation
Inventors:
Semiramis Ayral-Kaloustian, Joseph William Epstein, Gary H. Birnberg, Edward James Salaski, Gloria Jean Macewan, Katherine Cheung
Abstract: The invention provides methods and use of heterocyclic amines, and phenylazacycloalkane compounds, and their pharmacologically acceptable salts for the treatment of Restless Legs Syndrome (RLS).
Abstract: A method of treating and/or preventing allergic and inflammatory conditions of the skin or airway passages in a human in need of such treating and/or preventing which comprises administering to said human an effective amount of a nonsedating antihistamine for such treating and/or preventing while avoiding the side effects associated with other nonsedating antihistamines that bind to the P-glycoprotein pump and/or the organic anion transport polypeptide pump is disclosed.
Type:
Grant
Filed:
June 21, 2002
Date of Patent:
July 29, 2003
Assignee:
Schering Corporation
Inventors:
William W. Johnson, Er-Jia Wang, Christopher Casciano, Robert P. Clement
Abstract: The present invention provides:
an anti-HIV composition comprising at least one member selected from the group consisting of trifluridine and derivatives thereof, and a pharmaceutically acceptable carrier;
an anti-HIV composition comprising (a) at least one member selected from the group consisting of trifluridine and derivatives thereof, (b) a thymidine phosphorylase inhibitor, and a pharmaceutically acceptable carrier; and
a composition for potentiating the anti-HIV activity of trifluridine and derivatives thereof, comprising a thymidine phosphorylase inhibitor and a pharmaceutically acceptable carrier.
Abstract: A composition containing therapeutic agents and/or breath freshening agents for use in the oral cavity is disclosed. The carrier comprises water-soluble polymers in combination with certain ingredients and provides a therapeutic and/or cosmetic effect. The film is coated and dried utilizing existing coating technology and exhibits instant wettability followed by rapid dissolution/disintegration upon administration in the oral cavity.
Type:
Grant
Filed:
June 5, 2002
Date of Patent:
July 15, 2003
Assignee:
LTS Lohmann Therapie-Systeme AG
Inventors:
Horst Georg Zerbe, Jian-Hwa Guo, Anthony Serino
Abstract: The invention is directed to small organic molecules having the ability to mimic or agonize hepatocyte growth factor/scatter factor (HGF/SF) activity, or inhibit or antagonize HGF/SF activity, the former useful for promoting, for example, vascularization of tissues or organs for promoting wound or tissue healing, or augmenting or restoring blood flow to ischemic tissues such as the heart following myocardial infarction. Inhibition of cellular growth or proliferation is beneficial in the treatment, for example, of inflammatory diseases such as inflammatory joint and skin diseases, and dysproliferative diseases such as cancer.
Type:
Grant
Filed:
June 29, 2001
Date of Patent:
July 8, 2003
Assignee:
North Shore-Long Island Jewish Health System
Inventors:
Sivaram Pillarisetti, Itzhak D. Goldberg