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©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
Published online May 27, 2014. doi: 10.4254/wjh.v6.i5.326
RCT | Dose frequency | Duration | SVR | Possible AE |
SPRINT 1 | 12 pills for 3 intakes | 28-wk triple therapy vs 4-wk lead-in phase | 54%-56% | Metal taste, anemia |
48-wk triple therapy vs 4-wk lead-in phase | 67%-75% | |||
SPRINT 2 | 12 pills for 3 intakes | 28-48 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 therapy | 67% And 44% were given abridged AVT | Taste disturbances, anemia, neutropenia |
- Citation: Bakulin I, Pasechnikov V, Varlamicheva A, Sannikova I. NS3 protease inhibitors for treatment of chronic hepatitis C: Efficacy and safety. World J Hepatol 2014; 6(5): 326-339
- URL: https://www.wjgnet.com/1948-5182/full/v6/i5/326.htm
- DOI: https://dx.doi.org/10.4254/wjh.v6.i5.326