To evaluate safety and efficacy of GS-9857 plus sofosbuvir/velpatasvir for 12 weeks in treatment experienced genotype 1-6 HCV infected patients with and Without Cirrhosis.

Trial Profile

To evaluate safety and efficacy of GS-9857 plus sofosbuvir/velpatasvir for 12 weeks in treatment experienced genotype 1-6 HCV infected patients with and Without Cirrhosis.

Completed
Phase of Trial: Phase II

Latest Information Update: 06 Jan 2017

At a glance

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