
The U.S. Food and Drug Administration (FDA) has cleared Titan Pharmaceuticals’ (NASDAQ:TTNP) Investigational New Drug (IND) application for the Phase 1 study of its drug candidate Nalmefene.
The Phase 1 study will investigate six-month or longer subdermal formulation of nalmefene intended for the prevention of relapse following opioid detoxification in adults with Opioid Use Disorder (OUD).