drugset / Trial / NCT01343888

Efficacy and Safety of BI 201335 (Faldaprevir) in Combination With Pegylated Interferon-alpha and Ribavirin in Treatment-naïve Genotype 1 Hepatitis C Infected Patients (STARTverso 1)

NCT01343888 ↗

Phase 3 Completed 656 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this trial is to evaluate the efficacy and safety of two different treatment regimens with BI 201335, both in combination with PegIFN/RBV) as compared to standard of care (SOC) with PegIFN/RBV alone.

Timeline

Start
2011-04
Primary completion
2014-03
Completion
2014-03

Outcome

Met primary endpoint

registry analysis (superiority or other test); Faldaprevir 120mg and PegIFN/RBV vs Placebo and PegIFN/RBV; p <0.0001 NCT01343888 ↗

registry analysis (superiority or other test); Faldaprevir 240mg and PegIFN/RBV vs Placebo and PegIFN/RBV; p <0.0001 NCT01343888 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Faldaprevir Small molecule 120 mg —
Subject Faldaprevir Small molecule 240 mg —
Background Peginterferon Protein / enzyme biologic — Subcutaneous
Background Ribavirin Small molecule — Oral