drugset / Trial / NCT01215643

Efficacy and Safety of Alisporivir Alone or Combined With RBV or PEG in Chronic Hepatitis C Genotype 2 and 3 Treatment-naïve Participants

NCT01215643

Phase 2 Completed 340 enrolled Debiopharm International SA
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is to investigate whether alisporivir (ALV; DEB025) alone or in combination with either ribavirin (RBV) or peginterferon alfa-2a (PEG) is more efficient compared to standard of care (PEG+RBV) in treatment-naïve participants with hepatitis C virus (HCV) genotype 2 and 3. In addition, triple therapy with DEB025 plus standard of care will be applied to participants not achieving rapid viral response (RVR) in the different arms.

Timeline

Start
2010-10
Primary completion
2012-05
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Alisporivir Protein / enzyme biologic 600 mg Oral
Subject Alisporivir Protein / enzyme biologic 800 mg Oral
Subject Alisporivir Protein / enzyme biologic 1000 mg Oral
Subject Peginterferon alfa-2a Protein / enzyme biologic 180 ug Subcutaneous
Subject Ribavirin Small molecule 400 mg Oral