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Monday, June 28, 2021

Syndax Gets FDA Fast Track Designation for the Treatment of Relapsed/Refractory Acute Leukemias

 Syndax Pharmaceuticals, Inc. ("Syndax," the "Company" or "we") (Nasdaq: SNDX), a clinical stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation (FTD) to SNDX-5613 for the treatment of adult and pediatric patients with relapsed or refractory acute leukemias harboring a mixed lineage leukemia rearranged (MLLr) or nucleophosmin (NPM1) mutation. SNDX-5613 is the Company's highly selective, oral menin inhibitor.

https://finance.yahoo.com/news/sndx-5613-granted-fda-fast-110000364.html

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