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. 2016 Feb 3;36(8):1125–1132. doi: 10.1111/liv.13067

Figure 1.

Figure 1

Study design. This study consisted of a 12‐week treatment period followed by a 24‐week post‐treatment period. PTV/r, paritaprevir/ritonavir; RBV, ribavirin; SVR12, sustained virological response at post‐treatment week 12 (primary endpoint); SVR24, sustained virological response at post‐treatment week 24.