Combination therapies for cancer
AssigneesMerck Sharp & Dohme Corp., GlaxoSmithKline LLC
InventorsAxel Hoos, Keith W. Orford, Patrick Chun, Venkataraman Sriram, Elaine M. Pinheiro, Scot W. Ebbinghaus
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AssigneesMerck Sharp & Dohme Corp., GlaxoSmithKline LLC
InventorsAxel Hoos, Keith W. Orford, Patrick Chun, Venkataraman Sriram, Elaine M. Pinheiro, Scot W. Ebbinghaus
Estimating the term…
A novel combination comprising a B-Raf inhibitor, particularly 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, the MEK inhibitor N-{3-[3-cyclopropyl-5-(2-fluoro-4-iodo-phenylamino)6,8-dimethyl; -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 a PD-1 antagonist; pharmaceutical compositions comprising the same and methods of using such combinations and compositions in the treatment of conditions in which the inhibition of MEK and/or B-Raf and/or immune modulation through PD-1 is beneficial, e.g., cancer.
A combination comprising a PD-1 antagonist and one or both of a Compound A and a Compound B, wherein:
A combination comprising a PD-1 antagonist and one or both of a Compound A and a Compound B, wherein the Compound B is N-{3-[5-(2-Amino-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide methanesulfonate;
(canceled)
A pharmaceutical composition comprising a PD-1 antagonist, wherein the pharmaceutical composition comprises one or both of a Compound A and a Compound B together with a pharmaceutically acceptable diluent or carrier, and wherein:
A pharmaceutical composition comprising an anti-human PD-1 antibody or an antigen binding fragment thereof together with a pharmaceutically acceptable diluent or carrier, wherein the combination therapy comprises the pharmaceutical composition and one or both of a Compound A and a Compound B,
(canceled)
A method of treating cancer in a mammal comprising administering to said mammal a combination therapy, wherein the combination therapy comprises a therapeutically effective amount of a PD-1 antagonist and one or both of a therapeutically effective amount of a Compound A and a therapeutically effective amount of a Compound B, wherein:
(canceled)
Dependencies are inferred from the claim text.