This first-in-human (FIH) dose-escalation and dose-validation/expansion study will assess ziftomenib (KO-539), a menin-MLL(KMT2A) inhibitor, in patients with relapsed or refractory acute myeloid leukemia (AML).
Est. Enrollment: 60 participants
Study Start Date: Sep 12, 2019
Study Completion Date: Dec 31, 2022
Age: 18+ years
Gender: All
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