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Copyright ©2014 Baishideng Publishing Group Inc.
World J Hepatol. May 27, 2014; 6(5): 326-339
Published online May 27, 2014. doi: 10.4254/wjh.v6.i5.326
Table 3 Telaprevir: clinical parameters
RCTDose frequencyDurationSVRPossible AE
Prove 1Each 8 h, 6 t/d24 wk: 12 wk of triple therapy, 12 wk of conventional treatment61%Rash, anemia, nausea, diarrhea
AdvanceEvery 8 h, 6 t/d24-48 wk: 8-12 wk of viral response-based treatment followed by conventional treatment69%-75%Rash, anemia, nausea, diarrhea
IlluminateEvery 8 h, 6 t/d24-48 wk: 12 wks of viral response-based treatment: 12 wk of triple therapy followed by conventional treatment64%-92%Rash, anemia, nausea, diarrhea
OptimizeEvery 12 h, 6 t/d24-48 wk: 12 wk of viral response-based treatment: 12 wk of triple therapy followed by conventional treatment for 12 to 36 wk58%-81% (depending on fibrosis stage)Rash, anemia, nausea