Table 7.
Study | Population | Regimen | Overall SVR12 | Cirrhotic SVR12 |
---|---|---|---|---|
NIAID SYNERGY (6 or 12 weeks) | GT1, TN, cirrhosis allowed | SOF/LDV, 12 weeks | 100% | 100% |
(20/20) | (3/3) | |||
GT1, TN, noncirrhotic | SOF/LDV/GS-9669, 6 weeks | 95% | n/a | |
(19/20) | ||||
GT1, TN, noncirrhotic | SOF/LDV/VDR, 6 weeks | 100% | n/a | |
(20/20) | ||||
BMS FOURWARD (4 or 6 weeks) | GT1, TN, noncirrhotic | DCV/ASV/BMS-791325 + SOF, 4 weeks | Pending | n/a |
GT1, TN, noncirrhotic | DCV/ASV/BMS-791325 + SOF, 6 weeks | Pending | n/a |
ASV, asunaprevir; DCV, daclatasvir; GT, genotype, SOF, sofosbuvir; TN, treatment naïve; LDV, ledipasvir; n/a, not applicable; VDR, vedroprevir.