Abstract: The present invention relates to a method for the treatment and/or amelioration of atopic dermatitis, the method including the administration of a pharmaceutically active dose of a compound selected from miltefosine, edelfosine, perifosine and ilmofosine to a subject in need of such a treatment and/or amelioration.
Type:
Grant
Filed:
December 20, 2006
Date of Patent:
August 16, 2011
Assignee:
Jado Technologies GmbH
Inventors:
Tobias Braxmeier, Tim Friedrichson, Gary Jennings
Abstract: The present invention features methods of treating a mammalian subject having renal cancer by administration of certain dimethylsulfonate compounds, such as a 4-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]-benzaldehyde. The present invention further features administration protocols and dosing schedules for methods of treating patients having renal cancer and pharmaceutical compositions suitable for use in the treatment methods provided herein.
Type:
Grant
Filed:
October 14, 2005
Date of Patent:
August 2, 2011
Assignee:
The United States of America as represented by the Secretary, Department of Health and Human Services
Inventors:
Susan D. Mertins, Susan Elaine Bates, David G. Covell, Geoffrey W. Patton, Melinda G. Hollingshead, Rao Vishnuvajjalla
Abstract: The present invention describes a combination of an anticholinergic, such as R,R-glycopyrrolate, and a ? mimetic, such as tormoterol, for the treatment of respiratory diseases including airway inflammation or obstruction such as chronic obstructive pulmonary disease (COPD) and asthma.
Type:
Grant
Filed:
July 30, 2007
Date of Patent:
July 26, 2011
Assignee:
MEDA Pharma GmbH & Co. KG
Inventors:
Joachim Goede, Joachim Maus, Peter Jurgen Cnota, Istvan Szelenyi
Abstract: The present invention is related to novel oral compositions comprising an irreversible gastric H+/K+-ATPase proton pump inhibitor (PPI) as a gastric acid secretion inhibitor and one or more small carboxylic acid molecules as parietal cell activators in the gastric lumen. Unexpectedly, the compositions of the present invention are capable of enhancing the anti-acid activity of PPI in the stomach. The present invention further relates to a method of using such compositions to reduce gastric acid secretion in a mammal.
Type:
Grant
Filed:
May 14, 2008
Date of Patent:
July 19, 2011
Assignee:
Vecta, Ltd.
Inventors:
Aleksey Kostadinov, David Ayelet, Sabina Glozman, Tal Atarot
Abstract: To provide a therapeutic agent for viral myocarditis and viral myocarditis-related viral diseases by treating the occurrence of cell damage in various organs regardless of the type of virus. A therapeutic agent for viral myocarditis and viral myocarditis-related viral diseases is provided that has as an active ingredient 2-[4-(dipehnylmethyl)-1-piperazinyl]-acetic acid, amide derivative, individual optical isomer or pharmaceutically acceptable salt thereof.
Abstract: The present invention relates to the use of metabotropic glutamate receptor 5 antagonists for the inhibition of transient lower esophageal sphincter relaxations. A further aspect of the invention is directed to the use of metabotropic glutamate receptor 5 antagonists for the treatment of gastroesophageal reflux disease, as well as for the treatment of regurgitation.
Type:
Grant
Filed:
June 19, 2003
Date of Patent:
June 21, 2011
Assignee:
AstraZeneca AB
Inventors:
Anders Lehmann, Jan Mattsson, Thomas M. Stormann
Abstract: A method for the therapeutic treatment of psoriasis by the administration of an anti-psoriasis effective amount of Doxivir (CTC-96) is discloses.
Abstract: The present invention concerns methods useful in treating a subject having diarrhea-predominant IBS (IBS-D) by administering N methyl-N-[(1S)-1-phenyl-2-((3S)-3-hydroxypyrrolidin-1-yl)ethyl]-2,2-diphenylacetamide and/or a pharmaceutically acceptable salt thereof to the subject.
Abstract: The invention relates to long-chain inulin and its preparation from artichoke roots, its use in foodstuffs and cosmetic preparations and foodstuffs and cosmetic preparations having the long-chain inulin.
Type:
Grant
Filed:
April 12, 2006
Date of Patent:
June 14, 2011
Assignee:
Bayer CropScience AG
Inventors:
Elke Hellwege, Roger Peeters, Jens Pilling
Abstract: The invention is directed to a method for treating hypertriglyceridemia, dyslipidemia and hypercholesterolemia by administration of a 1-methylnicotinamide salt.
Abstract: There is provided a method of reducing pain associated with colonic viscerosensitivity and spasticity induced during a colonic examination chosen from colonic endoscopy, barium/air contrast colonic radiography and virtual colonoscopy of a non-sedated patient.
Abstract: Methods of ameliorating episodes of accute or chronic colitis are provided by using methimazole derivatives and tautomeric cyclic thiones in combination with another pharmaceutical compound.
Type:
Grant
Filed:
August 6, 2004
Date of Patent:
April 19, 2011
Assignee:
Ohio University
Inventors:
Leonard D. Kohn, Douglas J. Goetz, Uruguaysito Benavides-Peralta, Mariana Gonzalez-Murguiondo, Norikazu Harii, Christopher J. Lewis, Giorgio Napolitano, Nilesh D. Dagia
Abstract: The invention relates to the use of a compound of the formula (I) for the treatment of bacterial infections caused by mycobacteria, nocardia or corynebacteria, wherein E is phosphorus; X1, X2 and X3 are oxygen; and R1 and R2 are as defined in the specification.
Type:
Grant
Filed:
February 6, 2009
Date of Patent:
April 12, 2011
Assignee:
Sanofi-Aventis
Inventors:
Gerhard Seibert, Luigi Toti, Joachim Wink
Abstract: A method for suppressing the number of peripheral blood lymphocytes involving administering to a human in need thereof a pharmaceutically effective amount of a compound which is (2R) -2-amino-2-methyl-4-{1-methyl-5-[4-(4-methylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol or a pharmacologically acceptable salt thereof, such as the hydrochloride salt.
Abstract: Methods are provided directed to administering a therapeutically effective amount of a prostaglandin EP4 agonist component to a mammal afflicted with or prone to afflicted with a disease or condition selected from an esophageal ulcer, alcohol gastropathy, a duodenal ulcer, non-steroidal anti-inflammatory drug-induced gastropathy, non-steroidal anti-inflammatory drug-induced enteropathy and intestinal ischemia. Such administration results in treating the disease or condition.
Type:
Grant
Filed:
November 30, 2005
Date of Patent:
February 22, 2011
Assignee:
Allergan, Inc.
Inventors:
Guang-Liang Jiang, Wha Bin Im, Larry A. Wheeler
Abstract: This invention concerns compositions for the treatment of urinary frequency, urinary urgency and urinary incontinence comprising (R)-N-[4-[2-[[2-hydroxy-2-(pyridin-3 -yl)ethyl]amino]ethyl]phenyl]-4-[4-(4-trifluoromethylphenyl)thiazol-2-yl]benzenesulfonamide and pharmaceutically acceptable salts thereof. In another aspect, this invention concerns combination therapy for urinary frequency, urinary urgency and urinary incontinence wherein one of the active agents is (R)-N-[4-[2-[[2-hydroxy-2-(pyridin-3-yl)ethyl]amino]ethyl]phenyl]-4-[4-(4-trifluoromethylphenyl)thiazol-2-yl]benzenesulfonamide and pharmaceutically acceptable salts thereof.
Type:
Grant
Filed:
September 29, 2006
Date of Patent:
February 22, 2011
Assignee:
Merck Sharp & Dohme Corp.
Inventors:
Keith M. Gottesdiener, Stuart A. Green, Euan MacIntyre
Abstract: Methods are provided for treating chronic obstructive pulmonary diseases such as emphysema using compounds that activate the signaling pathways of hepatocyte growth factor.
Abstract: Methods for the treatment of inflammatory and ulcerative diseases of the bowel (e.g., Crohn's disease and ulcerative colitis) with a therapeutically effective dose less than 50 mg. of opioid antagonists (e.g., naltrexone, nalmefene or naloxone) are disclosed. An embodiment of the invention includes a method of pharmaceutical treatment comprising orally administering to a human subject having Crohn's disease or ulcerative colitis a therapeutic pharmaceutical composition once per day in the evening or at bedtime, wherein the pharmaceutical composition comprises form about 3 mg to about 4.5 mg of naltrexone, nalmefene, naloxone, or a hydrochloride salt thereof in an immediate release solid dosage formulation.
Type:
Grant
Filed:
April 16, 2007
Date of Patent:
February 1, 2011
Inventors:
Jill P. Smith, Ian S. Zagon, Moshe Rogosnitzky
Abstract: The invention relates to a method of treating muscular dystrophy, such as a muscular dystrophy or myopathy resulting from mutations in genes encoding collagen VI, in a mammal. The method involves administering of a compound of the formula (I) or a pharmaceutically acceptable addition salt thereof to the mammal.