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Clinical Trial Summary

The primary objective of this study is to evaluate the antiviral efficacy of treatment with ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) therapy at the time of liver transplantation and through 4 weeks posttransplant in adults with genotype 1 or 4 hepatitis C virus (HCV) infection who are undergoing primary liver transplantation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02350569
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 2
Start date May 22, 2015
Completion date April 22, 2016

See also
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