APRINOIA Therapeutics Announces Fast Track Designation Granted by U.S. FDA to APN-1607 for the Diagnosis of Progressive Supranuclear Palsy
Fast Track Designation follows announcement in January 2024 that the U.S. Food and Drug Administration (FDA) granted a “Study May Proceed” letter for APRINOIA’s planned Phase 3 study of APN-1607 (florzolotau (18F)) in the U.S., U.K., Europe and Asia CAMBRIDGE, Mass., May 21 (Korea Bizwire) — APRINOIA Therapeutics Inc. (“APRINOIA” or the “Company”), a clinical-stage [...]