EMA grants accelerated review status to Gilead's new hepatitis C therapy

20 January 2017

USA-based biotech firm Gilead Sciences (Nasdaq: GILD) has received notice that the European Medicines Agency (EMA) has validated and will review its Marketing Authorization Application for a new hepatology product.

The investigational combination therapy of sofosbuvir, velpatasvir and voxilaprevir has been developed for the treatment of chronic hepatitis C. Choose

The EMA will review the therapy according to an accelerated procedure established for technologies that are expected to be of major public health interest.

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