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FDA grants regular approval to venetoclax in combination for untreated acute myeloid leukemia

22 Oct 2020 10:12 AM | Anonymous

The U.S. Food and Drug Administration granted regular approval to venetoclax (VENCLEXTA ®, AbbVie Inc. and Genentech Inc.) in combination with azacitidine, decitabine, or low-dose cytarabine (LDAC) for newly-diagnosed acute myeloid leukemia (AML) in adults 75 years or older, or who have comorbidities precluding intensive induction chemotherapy. Read full press release.

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