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

Drugs

EvaluationDrugModalityDoseRoute
Subject Faldaprevir Small molecule 120 mg
Subject Faldaprevir Small molecule 240 mg
Background Peginterferon alfa-2a Protein / enzyme biologic Subcutaneous
Background Ribavirin Small molecule Oral