EC approves label expansion for Enanta’s Maviret in acute HCV infection
The European Commission (EC) has approved Maviret (glecaprevir/pibrentasvir) for the treatment of acute hepatitis C virus (HCV) infection in adults and children aged 3 years and older without cirrhosis or with compensated cirrhosis, reported US drugmaker Enanta Pharmaceuticals (Nasdaq: ENTA), whose shares closed up 5.2% at $14.06 on the news yesterday.
This approval makes Maviret the sole treatment available in the European Union for both acute and chronic HCV infection, the company noted. Maviret is an oral, pangenotypic direct-acting antiviral (DAA) therapy that has been developed under a collaboration with US pharma major AbbVie (NYSE: ABBV).
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