drugset / Trial / NCT01740791

Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Velpatasvir in Participants With Chronic HCV Infection

NCT01740791

Phase 1 Completed 103 enrolled Gilead Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to evaluate the safety, tolerability, and antiviral activity of velpatasvir (formerly GS-5816) in HCV treatment naive participants with genotypes 1-6.

Timeline

Start
2012-11-06
Primary completion
2013-03-15
Completion
2014-01-24

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject velpatasvir Other / unclassified 5 mg Oral
Subject velpatasvir Other / unclassified 25 mg Oral
Subject velpatasvir Other / unclassified 50 mg Oral
Subject velpatasvir Other / unclassified 100 mg Oral
Subject velpatasvir Other / unclassified 150 mg Oral
Subject velpatasvir Other / unclassified 400 mg Oral