drugset / Trial / NCT01500616
Telaprevir Open-Label Study in Co-Infected Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Telaprevir | Small molecule | 750 mg | Oral |
| Subject | Telaprevir | Small molecule | 1125 mg | Oral |