AbbVie (ABBV) announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use adopted a positive opinion recommending the approval of Maviret, an oral pangenotypic direct-acting antiviral therapy for the treatment of acute hepatitis C infection in adults and children aged 3 years and older. The final European Commission decision is expected in the third quarter of 2026. If approved, Maviret would be indicated for both acute and chronic hepatitis C infection in the European Union.
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