| CPC A61K 31/5517 (2013.01) [A61K 31/145 (2013.01); A61K 31/4045 (2013.01); A61K 31/454 (2013.01); A61K 31/501 (2013.01); A61K 31/502 (2013.01); A61K 31/517 (2013.01); A61K 31/5377 (2013.01); A61K 45/06 (2013.01); A61P 35/00 (2018.01); G01N 33/6893 (2013.01); G01N 2333/4703 (2013.01)] | 5 Claims |
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1. A method for the treatment of a cancer, which comprises administering to a subject in need of such treatment:
a) a pharmaceutically effective amount of a compound that increases the amount of NAD+ in the subject's cancer cells, and
b) a pharmaceutically effective amount of a PARG inhibitor and optionally one or more PARP inhibitors, wherein the compound that increases the amount of NAD+ comprises dihydronicotinamide riboside (NRH), the PARG inhibitor comprises (E)-1-(((p-Tolylthio)imino)methyl) naphthalen-2-ol, and the cancer is a glioma.
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