drugset / Trial / NCT00987337
Filibuvir In Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Subjects
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective for this study is to determine if the addition of filibuvir to a standard regimen of peginterferon/ribavirin (pegIFN/RBV) significantly increases the proportion of subjects who achieve a sustained viral response (SVR) compared to peginterferon/ribavirin (pegIFN/RBV) therapy alone.
Timeline
- Start
- 2009-11
- Primary completion
- 2012-01
- Completion
- 2012-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Filibuvir | Small molecule | 300 mg | — |
| Subject | Filibuvir | Small molecule | 600 mg | — |