Pulmatrix, Inc. today announced the U.S. Food and Drug Administration (“FDA”) has accepted the PUR3100 investigational new drug (“IND”) application and the Company has received a study may proceed letter for a Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Single Event Study to Evaluate the Safety, Tolerability, and Efficacy of PUR3100 (Dihydroergotamine Mesylate Inhalation Powder) in the Acute Treatment of Migraine.
September 19, 2023
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