AbbVie IncEuropean Commission approval expands MAVIRET label to acute hepatitis C, the only therapy cleared for both acute and chronic HCV in EU.
The European Commission has approved AbbVie's MAVIRET for the treatment of acute hepatitis C virus infection, making it the only therapy cleared in the European Union for both acute and chronic HCV. The approval was supported by a Phase 3 study in which 96.2% of patients achieved sustained virological response 12 weeks post-treatment. MAVIRET combines glecaprevir, discovered by Enanta Pharmaceuticals, and pibrentasvir, and is already approved for chronic HCV. Enanta earns royalties on AbbVie's sales of the drug, which is sold as MAVYRET in the U.S. and MAVIRET elsewhere.
AbbVie IncEuropean Commission approval expands MAVIRET label to acute hepatitis C, the only therapy cleared for both acute and chronic HCV in EU.
Enanta Pharmaceuticals IncEnanta earns royalties on AbbVie's MAVIRET sales; expanded approval likely increases sales volume, boosting royalty revenue.