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FDA Grants Orphan Drug Designation for Ocifisertib to Treat Patients With AML

Currently, ocifisertib is being evaluated in a phase 1b and 2 trial to confirm the safety and tolerability profiles in patients with acute myeloid leukemia.

Treadwell Announces Ocifisertib, a First-in-Class PLK4 Inhibitor, has Received Orphan Designation from U S FDA for the Treatment of Acute Myeloid Leukemia

Treadwell Announces Ocifisertib, a First-in-Class PLK4 Inhibitor, has Received Orphan Designation from U S FDA for the Treatment of Acute Myeloid Leukemia
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