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Clinical Trial Summary

The primary objective of this study is to evaluate the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir (SOF/VEL) fixed-dose combination (FDC) for 12 weeks in participants with chronic hepatitis C virus (HCV) infection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02722837
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 3
Start date April 4, 2016
Completion date September 13, 2017

See also
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