Oncology Central

FDA approves TIBSOVO® for acute myeloid leukemia subtype

The FDA has granted approval for the first oral, targeted therapy for relapsed/ refractory acute myeloid leukemia (R/R AML) adults patients and an IDH1 mutation as detected by an FDA approved test. The approval of TIBSOVO® (ivosidenib) is based on Phase I study results.
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