drugset / Trial / NCT01500616

Telaprevir Open-Label Study in Co-Infected Patients

NCT01500616

Phase 3 Completed 122 enrolled Janssen-Cilag International NV
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to collect safety and tolerability data on telaprevir treatment in combination with Peg-IFN-alfa and RBV in patients with HIV/genotype 1 chronic HCV coinfection with severe fibrosis or compensated cirrhosis who are not eligible for enrollment into an ongoing clinical study of telaprevir.

Timeline

Start
2012-06
Primary completion
2014-08
Completion
2014-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Telaprevir Small molecule 750 mg Oral
Subject Telaprevir Small molecule 1125 mg Oral