Review
Copyright ©The Author(s) 2015.
World J Hepatol. Jul 28, 2015; 7(15): 1921-1935
Published online Jul 28, 2015. doi: 10.4254/wjh.v7.i15.1921
Table 9 Simeprevir
Ref.nDesignTreatmentPopulationOutcome
Fried et al[80]338Phase 2b double blind, placebo controlled randomized clinical trialSimeprevir PEGIFN-α-2a/RBVTreatment-naıve patients with HCV genotype 1 infection.Simeprevir in combination with PEGIFN/RBV significantly improved SVR rates and shortened therapy duration. Depression occurred in 10.4% of patients on simeprevir and 18.2% on standard treatment
Zeuzem et al[79]396Placebo controlled, randomized clinical trialSimeprevir, PEGIFN-α-2a/RBVpatients with HCV genotype-1 infection previously treated with PEGIFN/RBV12, 24, or 48 wk simeprevir with 48 wk PEGIFN/RBV significantly increased rates of SVR and was generally well tolerated. Depression occurred in 2/396 simeprevir patients
Jacobson et al[81]394Phase 3, randomized, double blind, placebo controlled multicenter clinical trialSimeprevir, PEGIFN-α-2a/RBVTreatment naïve patients with HCV genotype 1Simeprevir with PEGIFN-α-2a/RBV shortens therapy without worsening the adverse event profiles associated with PEGIFN
Manns et al[82]257Phase 3 multicenter randomized, placebo controlled clinical trialSimeprevir PEGIFN-α-2a or 2b/RBVTreatment-naive patients with HCV genotype 1 infectionAddition of simeprevir to PEGIFN-α-2a or PEGIFN-α-2b plus RBV improved SVR without worsening the known adverse events associated with peginterferon
Kumada et al[83]79Open label non comparative multicenter trialSimeprevir PEGIFN-α-2b/RBVHCV genotype 1 - treatment-naïve or had previously received IFN-based therapySimeprevir combined with PEGIFN-α-2b/RBV was effective across both groups. One patient in the control group receiving standard therapy alone discontinued due to grade 2 depression