drugset / Trial / NCT00987337

Filibuvir In Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Subjects

NCT00987337

Phase 2 Completed 288 enrolled Pfizer
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

EvaluationDrugModalityDoseRoute
Subject Filibuvir Small molecule 300 mg
Subject Filibuvir Small molecule 600 mg