Journal
HEPATOLOGY RESEARCH
Volume 45, Issue 5, Pages 501-513Publisher
WILEY
DOI: 10.1111/hepr.12375
Keywords
chronic hepatitis C; direct-acting antiviral; protease inhibitor; simeprevir (TMC435); sustained virologic response
Categories
Funding
- Janssen Pharmaceutical
- Janssen Research and Development
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AimThe efficacy and safety of simeprevir in combination with peginterferon--2b and ribavirin (PEG IFN--2b/RBV) were investigated in patients infected with hepatitis C virus (HCV) genotype 1 who were treatment-naive or had previously received interferon (IFN)-based therapy. MethodsCONCERTO-4 (NCT01366638) was an open-label, non-comparative, multicenter study of once-daily simeprevir (TMC435) 100mg in combination with PEG IFN--2b/RBV in treatment-naive and -experienced patients (prior relapsers or non-responders to IFN-based therapy) with chronic HCV genotype 1 infection. Twelve-week combination treatment was followed by 24/48-week response-guided PEG IFN--2b/RBV therapy for treatment-naive patients and prior relapsers, and 48-week PEG IFN--2b/RBV therapy for prior non-responders. Patients were followed for 72 weeks after treatment initiation. The proportions of patients with sustained viral response (SVR; undetectable HCV RNA) at treatment end and 12 weeks after the last treatment (SVR12) were among the major efficacy end-points. Safety, including adverse events (AE), was monitored. ResultsOf the 79 patients treated, the proportion achieving SVR12 was highest among treatment-naive patients (91.7%) and prior relapsers (100%) versus 38.5% of prior non-responders. All treatment-naive patients and prior non-responders who achieved SVR12 also achieved SVR at treatment end and 24 weeks after last dose; 96.6% of prior relapsers achieved both end-points. Most AE were of grade 1 or 2 severity. Grade 3 AE occurred in 17 patients, most frequently neutropenia (6.3%). ConclusionSimeprevir combined with PEG IFN--2b/RBV was effective in patients infected with HCV genotype 1, both for initial treatment of naive patients and for retreatment of patients in whom previous IFN-based therapy had failed.
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