Abstract: The present invention is directed to a method of treating a subject with autism spectrum disorder by administering an acetylaminopropane sulfonate.
Type:
Grant
Filed:
February 12, 2010
Date of Patent:
October 11, 2016
Assignee:
Indiana University Research & Technology Corporation
Abstract: Provided are methods of treating heart failure in children using B1-selective adrenergic receptor antagonists, alone or in combination with other agents, including B-2-selective adrenergic receptor agonists.
Type:
Grant
Filed:
August 25, 2011
Date of Patent:
October 4, 2016
Assignee:
THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE
Inventors:
Brian Stauffer, Carmen Sucharov, Shelley Miyamoto
Abstract: An anise flavored liquid medication. The liquid medication contains phenylephrine and an anethole analog that is substantially free of aldehyde groups. In one example, the anethole analog can be 1-methoxy-4-n-propylbenzene.
Type:
Grant
Filed:
February 13, 2014
Date of Patent:
October 4, 2016
Assignee:
The Procter & Gamble Company
Inventors:
Allyn Michael Kaufmann, James Carl Grimm, Chelsay Lynn Brewster, Thomas Edward Huetter
Abstract: Disclosed herein is a fungicidal composition comprising combination of fungicidally effective amount of mancozeb and a fungicidally effective amount of chlorothalonil in a predetermined ratio.
Type:
Grant
Filed:
September 25, 2013
Date of Patent:
September 27, 2016
Assignee:
UPL Limited
Inventors:
Jaidev Rajnikant Shroff, Vikram Rajnikant Shroff, Philip Wayne Robinson, Beth Errickson Sears, Prakash Mahadev Jadhav
Abstract: The present invention includes methods and compositions useful for treating and preventing skin disorders, hair loss and other skin disorders. The compositions include an ARD enhancer in combination with a second compound or composition. In some embodiments the second compound is at least one of a bactericide, an antibiotic, an anti-microbial peptide, Vitamin A, a Vitamin A derivative, a retinoid, an anti-inflammatory compound, and anti-androgen compounds.
Type:
Grant
Filed:
July 31, 2008
Date of Patent:
September 20, 2016
Assignee:
AndroScience Corporation
Inventors:
Charles C. Y. Shih, Ching-Yuan Su, Hui-Kang Wang, Qian Shi
Abstract: A method for treating core binding factor (CBF) leukemia in a subject, comprising administering to a subject having CBF leukemia a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt or ester thereof, that inhibits CBF? and RUNX1 binding in the subject, thereby treating the CBF leukemia.
Type:
Grant
Filed:
March 15, 2012
Date of Patent:
September 20, 2016
Assignee:
The United States of America, as represented by the Secretary, Department of Health and Human Services
Inventors:
Pu Liu, Wei Zheng, Juan Marugan, Noel T. Southall, Lea Cunningham
Abstract: Metallocene compounds and pharmaceutical compositions containing these metallocene compounds are disclosed and described. Methods of treating cancer employing such metallocene compounds and pharmaceutical compositions also are provided.
Type:
Grant
Filed:
July 10, 2014
Date of Patent:
September 13, 2016
Assignee:
Chevron Philips Chemical Company, LP
Inventors:
Mark L. Hlavinka, Qing Yang, Mandi Michelle Murph
Abstract: The present invention relates to compounds and methods which may be useful as treatments of neuromuscular diseases such as muscular dystrophy, and as inhibitors of NF-?B for the treatment or prevention of muscular wasting disease, including muscular dystrophy.
Type:
Grant
Filed:
January 27, 2014
Date of Patent:
September 6, 2016
Assignee:
ReveraGen Biopharma, Inc.
Inventors:
John M. McCall, Eric Hoffman, Kanneboyina Nagaraju
Abstract: Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula I as follows: wherein A, B, G, Y, R1, R2, R3, and R4 are defined herein.
Type:
Grant
Filed:
July 2, 2014
Date of Patent:
September 6, 2016
Assignee:
Janssen Pharmaceutica, N.V.
Inventors:
Shawn T Branum, Raymond W Colburn, Scott L Dax, Christopher M Flores, Michele C Jetter, Yi Liu, Donald Ludovici, Mark J Macielag, Jay M Matthews, James J McNally, Laura M Andraka, Ronald K Russell, Ning Qin, Christopher Teleha, Kenneth M Wells, Scott C Youells, Mark A Youngman
Abstract: Methods and compositions of treating a subject for cancer pain are provided. In the subject methods, a subject is treated for cancer pain by administering to the subject an effective amount of a narcotic emulsion, e.g., fentanyl elmulsion, formulation. In certain embodiments, the emulsion formulations include a narcotic active agent, oil, water and a surfactant. Also provided are methods of making the subject emulsion formulations as well as kits that include the emulsion formulations.
Type:
Grant
Filed:
September 22, 2014
Date of Patent:
August 30, 2016
Assignees:
Teikoku Pharma USA, Inc., Techno Guard Co., Ltd.
Abstract: Compositions and methods for treating glaucoma are provided. In particular hydrophilic ester prodrugs and their use to reduce central corneal thickening is provided.
Abstract: Disclosed is as a substituted thiazolamine derivative represented by Formula I or a pharmaceutically acceptable salt thereof or a hydrate thereof (the definitions of each group in the formula are as presented in the description), and the application thereof in the prevention and/or treatment of viral diseases induced by picornavirus. Also disclosed is a pharmaceutical composition containing the compound.
Type:
Grant
Filed:
December 6, 2011
Date of Patent:
August 30, 2016
Assignee:
Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China
Abstract: The present invention is directed to BCAT inhibitors with the following formula: Wherein R1 is a linear alkyl group and X+ denotes a cation. These inhibitors are useful in treating autoimmune inflammatory diseases such as systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, psoriasis and inflammatory bowel disease.
Abstract: The invention relates to the use of a compound of Formula I for the treatment of protease-activated receptor mediated diseases by the administration of a compound of Formula I or a prodrug or metabolite thereof.
Type:
Grant
Filed:
September 23, 2011
Date of Patent:
August 23, 2016
Assignees:
The Broad Institute, Inc., Beth Israel Deaconess Medical Center, Inc.
Abstract: Provided herein are methods for using at least one histone deacetylase inhibitor to decrease cellular DNA repair activity, methods for monitoring the decrease of cellular DNA repair activity using at least one biomarker, methods of treating cancer by using at least one histone deacetylase inhibitor to decrease cellular DNA repair activity in combination therapy, methods of combination therapy where at least one histone deacetylase inhibitor interferes with a DNA repairing mechanism involving RAD51, methods for predicting a induction time period between a first administration of at least one histone deacetylase inhibitor and a second administration of at least one other therapeutic treatment, and pharmaceutical compositions for combination therapy.
Type:
Grant
Filed:
December 7, 2007
Date of Patent:
August 9, 2016
Assignee:
Pharmacyclics LLC
Inventors:
Shanthi Adimoolam, Joseph J. Buggy, Darren Magda, Richard Miller
Abstract: The present invention relates to a method of treating cancer in a human and to pharmaceutical combinations useful in such treatment. In particular, the method relates to a cancer treatment method that includes administering N-{3-[5-(2-Amino-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide or a pharmaceutically acceptable salt thereof, and N-{(1S)-2-amino-1-[(3,4-difluorophenyl)methyl]ethyl}-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-2-furancarboxamide, or a pharmaceutically acceptable salt thereof, to a human in need thereof.
Type:
Grant
Filed:
August 11, 2014
Date of Patent:
August 2, 2016
Assignee:
Novartis AG
Inventors:
Melissa Dumble, Tona Gilmer, Rakesh Kumar, Sylvie Laquerre, Peter F. Lebowitz, Shannon Renae Morris
Abstract: Small molecule inhibitors of 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) having the following formula: Formula (1) are provided herein. Also provided herein are pharmaceutical compositions containing Formula I compounds, together with methods of treating cancer, methods of inhibiting PFK.FB3 enzymatic activity, methods of inhibiting glycolytic flux, and methods of treating tumors by administering an effective amount of a Formula I compound.
Type:
Grant
Filed:
February 22, 2011
Date of Patent:
August 2, 2016
Assignees:
Advanced Cancer Therapeutics, LLC, University of Louisville Research Foundation, Inc.
Inventors:
Pooran Chand, Jason A. Chesney, Brian F. Clem, Gilles H. Tapolsky, Sucheta Telang, John O. Trent
Abstract: A method for preventing or treating a disease selected from the group consisting of visceral pain, inflammatory pain, osteoarthritis pain, neuropathic pain, and fibromyalgia in a subject in need thereof, comprising administering to said subject an effective amount of the compound of the following formula (I) or a salt thereof: wherein R1, R2, R3, R4, R5, X and n are as described herein.
Abstract: The present invention relates to new biphenyl-3-carboxylic acid modulators of beta-3-adrenoceptor activity, pharmaceutical compositions thereof, and methods of use thereof.
Abstract: This invention relates to solid oral pharmaceutical formulations of (S)-methyl (1-((4-(3-(5-chloro-2-fluoro-3-(methylsulfonamido)phenyl)-1-isopropyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)propan-2-yl)carbamate (COMPOUND A) and the use of the formulations for treating proliferative diseases, such as solid tumor diseases.
Type:
Grant
Filed:
November 21, 2012
Date of Patent:
July 12, 2016
Assignee:
Novartis AG
Inventors:
Daya Verma, Yogita Krishnamachan, Xiaohong Shen, Hanchen Lee, Ping Li, Rajinder Singh, LayChoo Tan