At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Safety, Pharmacokinetics and Antiviral Effect of BI 201335 NA in HCV-1 Infected Patients Treated for 28 Days for Treatment naïve and Experienced Patients Treated in Combination With Peg Interferon Alfa-2a and Ribavirin
In Brief
A Phase 2 clinical trial evaluating ribavirin (RBV), pegylated interferon (PegIFN) alfa-2a, and 5 other interventions for Hepatitis C and Pharmacokinetics. Completed, enrolled 22 participants across 3 sites.
Detailed Summary
The current Standard of Care (SOC) for chronic HCV infection, which is pegylated interferon-alfa as combination therapy with ribavirin for 24-48 weeks of treatment, is effective in only part of the patients and is often associated with severe adverse effects leading to discontinuation of treatment and dose modifications. A number of compounds with direct activity are currently under clinical development, incl. BI 201335. BI 201335 works by preventing the Hepatitis C virus from replicating by binding to the HCV protease (enzyme). The main purpose of this clinical trial with BI 201335 is to see how well BI 201335 works and how safe BI 201335 is to use daily in combination with PegIFN and RBV in HCV infected patients
Study Details
Timeline
Interventions
ribavirin (RBV)
pegylated interferon (PegIFN) alfa-2a
pegylated interferon (PegIFN) alfa-2a
ribavirin (RBV)
Placebo
pegylated interferon (PegIFN) alfa-2a
ribavirin (RBV)
BI 201335 NA high
BI 201335 NA
placebo
BI 201335 NA high