Abstract: Provided are compounds useful for treating cancer and methods of treating cancer comprising administering to a subject in need thereof a compound described herein.
Type:
Grant
Filed:
June 29, 2017
Date of Patent:
May 21, 2019
Assignee:
Agios Pharmaceuticals, Inc.
Inventors:
Giovanni Cianchetta, Byron DeLaBarre, Janeta Popovici-Muller, Francesco G. Salituro, Jeffrey O. Saunders, Jeremy Travins, Shunqi Yan, Tao Guo, Li Zhang
Abstract: The invention relates to a method of treating a subject who has suffered a myocardial infarction with ST-elevation and to a method of treating reperfusion injury in a subject, the method comprising intravenous administration of melatonin to the subject, wherein the administration is initiated within 3 hours or less of symptom onset and prior to the mechanical reperfusion and is maintained for at least 60 minutes.
Type:
Grant
Filed:
March 15, 2018
Date of Patent:
May 7, 2019
Inventors:
Alberto Domínguez Rodríguez, Pedro Abreu González
Abstract: Compounds having the following formula (I), or a stereoisomer or pharmaceutically-acceptable salt thereof, where R1, R2, R3, R4, and R5 are as defined herein, are useful in the modulation of IL-12, IL-23 and/or IFN?, by acting on Tyk-2 to cause signal transduction inhibition.
Type:
Grant
Filed:
December 10, 2014
Date of Patent:
April 30, 2019
Assignee:
Bristol-Myers Squibb Company
Inventors:
Chunjian Liu, James Lin, Ryan M. Moslin, David S. Weinstein, John S. Tokarski
Abstract: Disclosed is a pregabalin sustained-release preparation, wherein the sustained-release tablet contains a pharmaceutically active ingredient containing pregabalin or a salt or hydrate thereof, a gel framework material containing alginic acid, and a swellable material containing polyoxyethylene.
Abstract: The present invention provides certain cortexolone derivatives of formula (I), and the same for use as antitumor active ingredients for the curative or adjuvant, or neoadjuvant or palliative treatment of precancerous lesions, dysplasias, metaplasias and tumor diseases, including malignant neoplasias and metastasis. Another aspect of the invention relates to pharmaceutical compositions comprising cortexolone derivatives of formula (I) as active ingredients and at least one physiologically acceptable excipient, and to the use of said pharmaceutical compositions as antitumor medicinal products.
Abstract: A method of treatment of infection in a subject comprising administering to the subject a copolymer comprising an acrolein derived segment or a polyacrolein oligomer segment and a polyalkylene glycol oligomer segment, the copolymer having a molecular weight of no more than 1500 Daltons.
Type:
Grant
Filed:
November 17, 2015
Date of Patent:
March 12, 2019
Assignee:
RECCE PHARMACEUTICALS LIMITED
Inventors:
Graham John Hamilton Melrose, Michele Keryn Dilizia
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:
April 10, 2017
Date of Patent:
February 19, 2019
Assignee:
ReveraGen Biopharma, Inc.
Inventors:
John M. McCall, Eric Hoffman, Kanneboyina Nagaraju
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:
February 3, 2016
Date of Patent:
February 12, 2019
Assignee:
MARS, INCORPORATED
Inventors:
Stephen French, Amar P Inamdar, Ian Andrew MacDonald, Susan T Francis
Abstract: Described herein are methods for modulating the amount of a gene product and compounds for use in such methods. More particularly, described herein are methods for modulating the amount of an RNA transcript or protein product as the result of gene expression and compounds for use in such methods.
Abstract: The present invention provides small molecules for endothelial cell activation and compositions thereof and methods of making and using the same.
Type:
Grant
Filed:
February 23, 2012
Date of Patent:
February 5, 2019
Assignee:
The Regents of the University of California
Abstract: A pharmaceutical composition includes a therapeutically effective amount of exo-S-mecamylamine or a pharmaceutically acceptable salt thereof, substantially free of exo-R-mecamylamine in combination with a pharmaceutically acceptable carrier. Preferably the amount is about 0.5 mg to about 20 mg. Medical conditions are treated by administering a therapeutically effective amount of exo-S-mecamylamine or a pharmaceutically acceptable salt thereof, substantially free of its exo-R-mecamylamine, said amount being sufficient to ameliorate the medical condition.
Type:
Grant
Filed:
May 3, 2018
Date of Patent:
January 29, 2019
Assignee:
UNIVERSITY OF SOUTH FLORIDA
Inventors:
Douglas Shytle, Paul R. Sanberg, Mary Newman, Archie A. Silver
Abstract: The invention discloses statins compounds used as local intraosseous application for the treatment of ischemic diseases, in particular, discloses local intraosseous application of statin compounds in the treatment of peripheral ischemic diseases or cardio-cerebrovascular ischemic diseases.
Type:
Grant
Filed:
September 1, 2016
Date of Patent:
January 15, 2019
Assignee:
Peking University Third Hospital
Inventors:
Chunli Song, Yingsheng Xu, Jie Tan, Qi Guo, Can Liu
Abstract: The present invention is directed to novel pyrimidines, their derivatives, pharmaceutically acceptable salts, solvates and hydrates thereof. The compounds and compositions of the present invention have protein kinases inhibitory activities and are expected to be useful for the treatment of protein kinases and/or mutants mediated diseases and conditions.
Abstract: A composition comprising a bitter tastant and at least one sophorolipid and optionally a carrier; wherein the composition is edible and wherein the bitter taste of said bitter tastant is reduced. A method of reducing bitter taste attributed to a bitter tastant in an edible composition, said method comprising adding to said edible composition an effective amount of at least one sophorolipid and optionally a carrier; such that any bitter taste induced by the bitter tastant is reduced.
Type:
Grant
Filed:
December 22, 2016
Date of Patent:
December 18, 2018
Assignees:
The United States of America, as Represented by the Secretary of Agriculture, Monell Chemical Senses Center
Inventors:
Daniel Solaiman, Richard D. Ashby, Mehmet Hakan Ozdener, Alexander Bachmanov
Abstract: A composition containing essential oils of two different species of Origanum, emulsified in water extracts of four herbs. The composition may be useful for prevention and/or treating major infections by pathogens such as Trichomonas vaginalis, Gardnerella vaginalis, and Candida albicans. When the composition is administered as a vaginal douche, rapid restoration of lactobacillus colony may occur after the administration.
Type:
Grant
Filed:
July 20, 2017
Date of Patent:
December 18, 2018
Assignee:
King Abdulaziz University
Inventors:
Taha Abdullah Kumosani, Elie Kamil Barbour, Werner Krull
Abstract: There is described a pharmaceutical combination comprising oxybutynin or a pharmaceutically acceptable addition salt thereof, in a transdermal therapeutic system, and an acetylcholinesterase inhibitor, useful for safely treating hypocholinergic disorders of the central nervous system such as Alzheimer type dementia. In this combination, the acetylcholinesterase inhibitor (AChEI) is present at a dose that is higher than the maximal recommended dose, per unit form. In particular, the transdermal therapeutic system comprising oxybutynin is in combination with rivastigmine in a transdermal formulation or oral form.
Type:
Grant
Filed:
January 8, 2016
Date of Patent:
December 11, 2018
Assignee:
Chase Pharmaceuticals Corporation
Inventors:
Thomas N. Chase, Kathleen E. Clarence-Smith
Abstract: A ferrocenyl compound having the general formula (I): (I) Het is a substituted or unsubstituted heterocyclic moiety. L1, L2 and L3 are each a linker independently selected from alkylene, alkyleneoxy, alkyleneoxyalkylene, alkylenecarbonyl, alkyleneoxycarbonyl, alkyleneamido, alkyleneoxyamido, alkenylene, alkenyleneoxy, alkenylenecarbonyl, alkenyleneamido, alkynylene, alkynyleneoxy, alkynylenecarbonyl and alkynyleneamido, all of which may be straight chain or branched, substituted or unsubstituted. R1 and R2 are each independently selected from H, substituted or unsubstituted alkyl carbonyl, substituted or unsubstituted aryl carbonyl, substituted or unsubstituted phosphate, substituted or unsubstituted phosphonate and substituted or unsubstituted phosphoramidate. M and n are each 0 or 1 and m+n?0.1.
Type:
Grant
Filed:
December 19, 2014
Date of Patent:
November 27, 2018
Assignee:
THE UNIVERSITY OF BIRMINGHAM EDGBASTON
Inventors:
Chris Tselepis, James Tucker, Huy Van Nguyen, Nikolas John Hodges, Youcef Mehellou
Abstract: The invention is directed to compositions of vitamin D having enhanced bioavailability and enhanced stability. Methods of making and using the compositions of the invention are contemplated and disclosed.
Abstract: The invention relates to concentrated therapeutic phospholipid compositions; methods for treating or preventing diseases associated with cardiovascular disease, metabolic syndrome, inflammation and diseases associated therewith, neurodevelopmental diseases, and neurodegenerative diseases, comprising administering an effective amount of a concentrated therapeutic phospholipid composition.