CPC A61K 31/506 (2013.01) [A61K 31/423 (2013.01); A61K 31/4439 (2013.01); A61K 31/454 (2013.01); A61K 31/713 (2013.01); A61K 38/1761 (2013.01); A61K 38/45 (2013.01); A61K 39/3955 (2013.01); A61K 45/06 (2013.01); A61P 35/00 (2018.01); C07K 16/40 (2013.01); C12N 15/1137 (2013.01); C12Y 203/02 (2013.01); C07K 2317/24 (2013.01); C07K 2317/54 (2013.01); C07K 2317/55 (2013.01); C12N 2310/11 (2013.01); C12N 2310/14 (2013.01)] | 12 Claims |
1. A method for treating a human subject having, or at risk of developing, a cancer, the method comprising administering to the human subject an effective amount of a USP1 inhibitor and a PARP inhibitor, wherein the human subject is identified as having a BRCA1 and/or BRCA2 mutation.
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