drugset / Trial / NCT02350569

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed Dose Combination Administered in Patients Infected With Chronic Genotype 1 or 4 HCV for Use in the Peri-Operative Liver Transplantation Setting

NCT02350569 ↗

Phase 2 Completed 17 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2015-05-22
Primary completion
2016-03-28
Completion
2016-04-22

Drugs

EvaluationDrugModalityDoseRoute
Subject LDV/SOF Unknown 90 mg Oral
Subject LDV/SOF Unknown 400 mg Oral