Vosevi approval brings 'hope for hardest-to-treat' HCV patients

19 July 2017

The US Food and Drug Administration (FDA) has approved Vosevi (sofosbuvir/velpatasvir/voxilaprevir) for re-treatment of adults with chronic hepatitis C virus (HCV).

Vosevi is a fixed-dose, combination tablet from US biotech giant Gilead Sciences (Nasdaq: GILD) contains two previously approved drugs – sofosbuvir and velpatasvir – and a new drug, voxilaprevir.

"For patients who require re-treatment, there remains an unmet clinical need for an effective and well-tolerated option"

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