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Advisor(s)
Abstract(s)
BACKGROUND & AIMS: The efficacy and tolerability of faldaprevir, a potent hepatitis C virus (HCV) NS3/4A protease inhibitor, plus peginterferon (PegIFN) and ribavirin (RBV) was assessed in a double-blind, placebo-controlled phase 3 study of treatment-naïve patients with HCV genotype-1 infection.
METHODS:
Patients were randomly assigned (1:2:2) to PegIFN/RBV plus: placebo (arm 1, n = 132) for 24 weeks; faldaprevir (120 mg, once daily) for 12 or 24 weeks (arm 2, n = 259); or faldaprevir (240 mg, once daily) for 12 weeks (arm 3, n = 261). In arms 2 and 3, patients with early treatment success (HCV-RNA <25 IU/ml at week 4 and undetectable at week 8) stopped all treatment at week 24. Other patients received PegIFN/RBV until week 48 unless they met futility criteria. The primary endpoint was sustained virologic response 12 weeks post-treatment (SVR12).
RESULTS:
SVR12 was achieved by 52%, 79%, and 80% of patients in arms 1, 2, and 3, respectively (estimated difference for arms 2 and 3 vs. arm 1: 27%, 95% confidence interval 17%-36%; and 29%, 95% confidence interval, 19%-38%, respectively; p < 0.0001 for both). Early treatment success was achieved by 87% (arm 2) and 89% (arm 3) of patients, of whom 86% and 89% achieved SVR12. Adverse event rates were similar among groups; few adverse events led to discontinuation of all regimen components.
CONCLUSIONS:
Faldaprevir plus PegIFN/RBV significantly increased SVR12, compared with PegIFN/RBV, in treatment-naïve patients with HCV genotype-1 infection. No differences were seen in responses of patients given faldaprevir once daily at 120 or 240 mg.
Description
Keywords
Adult Antiviral Agents/administration & dosage Double-Blind Method Drug Therapy, Combination Female Genotype Hepacivirus/classification Hepatitis C, Chronic/virology Humans Interferon-alpha/administration & dosage Male Middle Aged Oligopeptides/administration & dosage Polyethylene Glycols/administration & dosage RNA, Viral/blood Recombinant Proteins/administration & dosage Ribavirin/administration & dosage Thiazoles/administration & dosage CHLC GAS Antiviral Agents/adverse effects Hepacivirus/drug effects Hepacivirus/genetics Hepatitis C, Chronic/drug therapy Interferon-alpha/adverse effects Oligopeptides/adverse effects Polyethylene Glycols/adverse effects Recombinant Proteins/adverse effects Ribavirin/adverse effects Thiazoles/adverse effects
Citation
J Hepatol. 2015 Jun;62(6):1246-55