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Clinical Trial Summary

This study is to evaluate the safety, tolerability, and antiviral efficacy of ledipasvir/sofosbuvir fixed dose combination (FDC) with or without ribavirin (RBV) administered for 12 or 24 weeks in treatment-experienced subjects with chronic genotype 1 hepatitis C virus (HCV) infection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01768286
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 3
Start date January 2013
Completion date February 2014

See also
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