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. 2012 Aug 13;75(4):931–943. doi: 10.1111/j.1365-2125.2012.04419.x

Table 3.

Interferon free combination strategies in development

Mechanism Drugs Trial phase Patients Virological response, end point References
Nucleoside polymerase +NS3 protease inhibitor Daclatasvir + asunaprevir II Genotype-1, null responders, USA RVR 64%, SVR 36% (n = 11) Lok et al. 2012 [58]
II Genotype-1b, null reponders, Japan SVR24 100% (n = 10) Chayama et al. 2012 [79]
Nucleoside polymerase inhibitor + RBV GS-7977 +RBV II Genotype-2 and -3, naïve RVR 100%, SVR 100% (n = 10) Gane et al. 2011 [51]
II Genotype-1, null responders SVR4 10% (n = 10) Gane et al. 2012 [52]
Nucleoside polymerase +NS3 protease inhibitor +Ribavirin BI201335 +BI207127 +RBV II Genotype -1, naïve RVR 100% (n = 17) Zeuzem et al. 2011 [90]
Nucleoside polymerase +NS3 protease inhibitor Tegobuvir +GS-9256 II Genotype-1, naïve EVR 80% (n = 15) +RBV: EVR 100%) (n = 13) Foster et al. 2011 [86]
Nucleoside polymerase +NS3 protease inhibitor Mericitabine +danoprevir II Genotype-1, experienced, non-responders Day14 viral load −4.9 log10 IU ml−1 Gane et al. 2010 [55]
II Genotype-1, naïve Day14 viral load −5.1 log10 IU ml−1 Gane et al. 2010 [55]

PEG-IFN, pegylated interferon alpha-2a/b; RBV, ribavirin; RVR, rapid virological response with HCV RNA undetectable at week 4; EVR, early virological response with HCV RNA undetectable at week 12.