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KOMZIFTI® (Ziftomenib)

January 11, 2026January 11, 2026 RR FDA Approvals
Acute Myeloid Leukemia

The FDA on November 13, 2025, approved KOMZIFTI®, a menin inhibitor, for adults with relapsed or refractory Acute Myeloid Leukemia (AML) with a susceptible Nucleophosmin 1 (NPM1) mutation who have no satisfactory alternative treatment options. KOMZIFTI® is a product of Kura Oncology, Inc.

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