drugset / Trial / NCT01958281

Sofosbuvir Plus Ribavirin, or Ledipasvir/Sofosbuvir in Adults With HCV Infection and Renal Insufficiency

NCT01958281

Phase 2 Completed 38 enrolled Gilead Sciences
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objectives of this study are to evaluate the safety and efficacy of sofosbuvir (SOF) plus ribavirin (RBV) for 24 weeks and ledipasvir/sofosbuvir (LDV/SOF) for 12 weeks, and to evaluate the steady state pharmacokinetics (PK) of SOF and its metabolites and LDV in participants with genotype (GT) 1, 3, or 4 hepatitis C virus (HCV) infection who have chronic renal insufficiency (impaired kidney function).

Timeline

Start
2013-10-07
Primary completion
2017-07-18
Completion
2017-10-19

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ledipasvir/Sofosbuvir Unknown 90 mg Oral
Subject Ledipasvir/Sofosbuvir Unknown 400 mg Oral
Subject Ribavirin Small molecule 200 mg Oral
Subject Sofosbuvir Small molecule 200 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral