| CPC A61K 31/52 (2013.01) [A61K 31/505 (2013.01); A61K 31/519 (2013.01); A61K 31/704 (2013.01); A61K 45/06 (2013.01); C07D 401/12 (2013.01); C07D 471/04 (2013.01); C07D 473/00 (2013.01); C07D 473/34 (2013.01); G01N 33/5011 (2013.01); G01N 33/574 (2013.01); G01N 2333/521 (2013.01); G01N 2333/525 (2013.01); G01N 2333/53 (2013.01); G01N 2333/5434 (2013.01); G01N 2333/9121 (2013.01); G01N 2333/96494 (2013.01)] | 19 Claims |
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1. A method of treating a hematologic malignancy in a human subject in need thereof, comprising orally administering to the subject twice daily about 25 mg to about 75 mg of a compound having the following structure or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof:
![]() wherein the hematologic malignancy is chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), CLL/SLL, indolent non-Hodgkin lymphoma (iNHL), peripheral T-cell lymphoma (PTCL), cutaneous T-cell lymphoma (CTCL), or follicular lymphoma (FL).
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