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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 5 Boceprevir: clinical parameters
RCTDose frequencyDurationSVRPossible AE
SPRINT 112 pills for 3 intakes28-wk triple therapy vs 4-wk lead-in phase54%-56%Metal taste, anemia
48-wk triple therapy vs 4-wk lead-in phase67%-75%
SPRINT 212 pills for 3 intakes28-48 wk: ''viral response-based treatment''; ''lead-in period''; if HCV RNA (-) by week 8 and 24, to stop at week 28; if HCV RNA (+), 20 wk of double therapy67% And 44% were given abridged AVTTaste disturbances, anemia, neutropenia