drugset / Trial / NCT01473056

Study to Assess Safety,Tolerability,Pharmacokinetics & Antiviral Activity of JTK-853 in Hepatitis C Virus Genotype 1 Infected Subjects

NCT01473056

Phase 1 Completed 29 enrolled Akros Pharma Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to determine the safety, tolerability, pharmacokinetics and anti-viral activity of JTK-853 in hepatitis C virus genotype 1 infected subjects based on reduction in viral load (HCV RNA level) from baseline to end of treatment, followed by genotypic resistance monitoring for up to one year after study drug treatment.

Timeline

Start
2010-08
Primary completion
2010-10
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject JTK-853 Small molecule