drugset / Trial / NCT02251717

Safety and Efficacy of Ledipasvir/Sofosbuvir (LDV/SOF) Fixed Dose Combination (FDC) for 12 or 24 Weeks in Kidney Transplant Recipients With Chronic HCV Infection

NCT02251717 ↗

Phase 2 Completed 114 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2014-10-14
Primary completion
2016-03-24
Completion
2016-06-16

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper no inferential statistics were planned PMID 27842383 ↗

Publications

Drugs

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