Kurt R. Auger - Collegeville PA, US Kurtis Earl Bachman - Collegeville PA, US Tona M. Gilmer - Research Triangle Park NC, US Joel David Greshock - Collegeville PA, US Sylvie Laquerre - King of Prussia PA, US Li Liu - King of Prussia PA, US Shannon Renae Morris - Research Triangle Park NC, US
Assignee:
GlaxoSmithKline LLC - Philadelphia PA
International Classification:
A61K 31/519 A61P 35/00
US Classification:
51425202
Abstract:
The present invention relates to a method of treating cancer in a mammal and to pharmaceutical combinations useful in such treatment. In particular, the method relates to a novel combination comprising the MEK inhibitor: N-{3-[3-cyclopropyl-5-[(2-fluoro-4-iodophenyl)amino]-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydropyrido[4,3-d]pyrimidin-1(2H)-yl]phenyl}acetamide, or a pharmaceutically acceptable salt or solvate thereof, and the PI3 kinase inhibitor: 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the same, and methods of using such combinations in the treatment of cancer.
Kurtis Earl Bachman - Collegeville PA, US Joel David Greshock - Collegeville PA, US
Assignee:
GlaxoSmithKline Intellectual Property Development Limited - Middlesex
International Classification:
A61K 31/501 A61K 45/06
US Classification:
51425204
Abstract:
The present invention provides a method of treating a human with cancer comprising detecting at least one mutation in a PIK3CA gene or at least one mutant protein encoded by said PIK3CA gene from at least one first sample from said human and administering to said human an effective amount of 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide or a pharmaceutically acceptable salt thereof in a pharmaceutical composition if said at least one sample has at least one mutant PI3K protein or a mutation in the PIK3CA gene.
Kurtis Earl Bachman - Collegeville PA, US Joel David Greshock - Collegeville PA, US Tona Gilmer - Research Triangle Park NC, US Sylvie Laquerre - King of Prussia PA, US Shannon Renae Morris - Research Triangle Park NC, US
International Classification:
A61K 31/506 A61P 35/00
US Classification:
51425204
Abstract:
The present invention relates to a method of treating cancer in a mammal and to pharmaceutical combinations useful in such treatment. In particular, the method relates to a novel combination comprising the MEK inhibitor: N-{3-[3-cyclopropyl-5-(2-fluoro-4-iodo-phenylamino)6,8-dimethy; -2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]phenyl}acetamide, or a pharmaceutically acceptable salt or solvate thereof, and the PI3 kinase inhibitor: 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the same, and methods of using such combinations in the treatment of cancer.
Small Molecule Inhibitor Of The Jak Family Of Kinases
- Beerse, BE Kurtis E. Bachman - Chester Springs PA, US Gerald C. Chu - Philadelphia PA, US Tatiana Koudriakova - Poway CA, US David C. Polidori - Rancho Santa Fe CA, US Gary V. Borzillo - Upper Gwynedd PA, US
Disclosed herein are JAK inhibitors that have low systemic toxicity. In some aspects, the disclosure includes methods for treating disease states, disorders, and conditions mediated by JAK, such as stomacho-intestinal system cancers, including colorectal cancers and familial adenomatous polyposis.
- Horsham PA, US Manuel Alejandro Sepulveda - West Windsor NJ, US Vipul Bhargava - Warrington PA, US Iqbal S. Grewal - Newtown PA, US Kurtis Bachman - Wayne PA, US