Abstract: A method of reducing pulmonary arterial hypertension in a mammal that employs FK506 is provided. In certain embodiments, the method comprises administering FK506 to a mammal having pulmonary arterial hypertension associated with defective MBPR2 signaling at a dosage sufficient to reduce blood pressure in the pulmonary artery of the mammal.
Type:
Grant
Filed:
April 30, 2012
Date of Patent:
October 25, 2016
Assignee:
The Board of Trustees of the Leland Stanford Junior University
Inventors:
Edda Spiekerkoetter, Marlene Rabinovitch, Philip A. Beachy, David Solow-Cordero
Abstract: The present invention relates generally to a sterile, particulate-free, stable intrathecal baclofen solution with less than 0.5% of 4-(4-chlorophenyl)-2-pyrrolidone, a degradation product. These solutions are stable under a variety of storage conditions and for extended periods of time. Also disclosed are methods for preparing such compositions.
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: 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: 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 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: According to the invention there is provided a method for the treatment of airway hyperresponsiveness, which method comprises the administration of pemirolast, or a pharmaceutically acceptable salt thereof, to a patient in need of such treatment. Suitable lower doses of pemirolast are least about 110 mg per day.
Type:
Grant
Filed:
November 24, 2015
Date of Patent:
August 16, 2016
Assignee:
RSPR Pharma AB
Inventors:
Johan Raud, Carl-Johan Dalsgaard, Göran Tornling
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: The invention provides methods and compounds for the treatment and prevention of malaria infection and transmission in a mammal by administering compounds of the invention to a mammal having or suspected of having a malaria infection. The invention also provides pharmaceutical compositions that can kill or arrest the growth of Plasmodium organisms, and especially Plasmodium falciparum, thereby preventing or blocking transmission of malaria as well as treating malaria infection.
Type:
Grant
Filed:
August 27, 2010
Date of Patent:
June 28, 2016
Assignee:
The United States of America, as represented by the Secretary, Dept. of Health and Human Services
Inventors:
Xin-zhuan Su, Jing Yuan, Dipak Raj, Sittiporn Pattaradilokrat, Ron Johnson, Ruili Huang
Abstract: The present invention describes methods of treating dementia comprising administering an effective daily dose of N-[2-(6-fluoro-1H-indol-3-yl)ethyl]-3-(2,2,3,3-tetrafluoropropoxy)benzylamine to improve or augment the effect of an acetylcholinesterase inhibitor.
Abstract: The present invention provides methods of treating, stabilizing or lessening the severity or progression of a disease or disorder associated with BTK.
Type:
Grant
Filed:
October 26, 2012
Date of Patent:
June 14, 2016
Assignee:
Celgene Avilomics Research, Inc.
Inventors:
Steven Richard Witowski, William Frederick Westlin, III, Heather Lounsbury, Kathryn Stiede, Bruce A. Silver, Jay M. Mei
Abstract: The present invention relates to pharmaceutical compositions, food supplement compositions and cosmetic compositions comprising diaminooxidase, and to the use thereof.
Type:
Grant
Filed:
April 4, 2014
Date of Patent:
June 14, 2016
Assignee:
SCIOTEC DIAGNOSTIC TECHNOLOGIES GMBH
Inventors:
Albert Missbichler, Franz Gabor, Herwig Reichl
Abstract: Compounds of Formula I are useful inhibitors of CDK 4, CDK6, and FLT3. Such compounds are useful in treating cancer and various other disease conditions. Compounds of Formula I have the following structure: where R1 is a group of Formula IA, Formula IB, Formula IC, or Formula ID and the definitions of the other variables are provided herein.
Type:
Grant
Filed:
November 25, 2013
Date of Patent:
June 7, 2016
Assignee:
AMGEN INC.
Inventors:
Xiaoqi Chen, Kang Dai, Jason Duquette, Michael W. Gribble, Jr., Justin N. Huard, Kathleen S. Keegan, Zhihong Li, Sarah E. Lively, Lawrence R. McGee, Mark L. Ragains, Xianghong Wang, Margaret F. Weidner, Jian Zhang
Abstract: The present invention relates to non-steroidal ligands for use in nuclear receptor-based inducible gene expression system, and a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA construct comprising; the exogenous gene and a response element; wherein the exogenous gene is under the control of the response element and binding of the DNA binding domain to the response element in the presence of the ligand results in activation or suppression of the gene.
Type:
Grant
Filed:
July 30, 2013
Date of Patent:
June 7, 2016
Assignee:
Intrexon Corporation
Inventors:
Robert Eugene Hormann, David W. Potter, Orestes Chortyk, Colin M. Tice, Glenn Richard Carlson, Andrew Meyer, Thomas R. Opie
Abstract: Embodiments herein relate to the field of lysosomal storage disorders, and, more specifically, to methods of treating lysosomal storage disorders such as Niemann-Pick type C disease, for instance with inhibitors of histone deacetylases, particularly inhibitors of class 1 histone deacetylases. In various embodiments, methods of treating Niemann-Pick type C disease with inhibitors of class 1 histone deacetylases are described.
Type:
Grant
Filed:
September 22, 2010
Date of Patent:
May 10, 2016
Assignees:
University of Notre Dame du Lac, Cornell University
Inventors:
Olaf Wiest, Frederick R. Maxfield, Paul Helquist
Abstract: The presently disclosed subject matter relates to pharmaceutical compositions comprising dexmedetomidine or a pharmaceutically acceptable salt thereof wherein the composition is formulated as a liquid for parenteral administration to a subject, and wherein the composition is disposed within a sealed container as a premixture. The pharmaceutical compositions can be used, for example, in perioperative care of a patient or for sedation.
Type:
Grant
Filed:
February 10, 2014
Date of Patent:
April 26, 2016
Assignee:
HOSPIRA, INC.
Inventors:
Priyanka Roychowdhury, Robert A. Cedergren
Abstract: The present disclosure relates to novel compounds having ?2 adrenergic agonist and M3 muscarinic antagonist dual activity, to pharmaceutical compositions containing them, to the process for their preparation and to their use in respiratory therapies.
Type:
Grant
Filed:
May 13, 2011
Date of Patent:
April 19, 2016
Assignee:
Almirall, S.A.
Inventors:
Maria Prat Quinones, Silvia Fonquerna Pou, Carlos Puig Duran, Wenceslao Lumeras Amador, Jose Aiguade Bosch, Juan Francisco Caturla Jovaloyes
Abstract: The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.
Abstract: This invention relates to compositions, and methods of use thereof, for (i) enhancing executive cognitive function(s) (for example, decision making, planning, working memory, multitasking, judgment, numerical problem-solving, reading comprehension), and/or (ii) increasing blood flow in brain vasculature, comprising administering to a subject in need thereof, certain polyphenols such as flavanols, procyanidins, or pharmaceutically acceptable salts or derivatives thereof.
Type:
Grant
Filed:
June 15, 2007
Date of Patent:
March 15, 2016
Assignee:
MARS, INCORPORATED
Inventors:
Stephen French, Amar P. Inamdar, Ian Andrew Macdonald, Susan T. Francis