European Medicines Agency has validated its MAA for new Gilead’s pill for Hepatitis C treatment
Gilead Sciences, Inc. announced this Friday that the company’s Marketing Authorization Application (MAA) for the investigational, once-daily, single tablet regimen of sofosbuvir 400 mg, velpatasvir 100 mg and voxilaprevir 100 mg (SOF/VEL/VOX) for the treatment of chronic ...