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Clinical Trial Summary

This study will evaluate the safety, tolerability, and antiviral efficacy of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) for 12 or 24 weeks in adults with chronic genotype 1 or genotype 4 hepatitis C virus (HCV) infection who have had a kidney transplant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02251717
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 2
Start date October 14, 2014
Completion date June 16, 2016

See also
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