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Boceprevir and telaprevir for the treatment of chronic hepatitis C genotype 1 infection: an indirect comparison meta-analysis

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Figure

Figure 1 Study flow diagram.
Table 4 Direct comparison of the proportion of patients achieving a sustained virologic response, relapsing to treatment, or discontinuing treatment in the trial intervention (telaprevir provided at a dose of 750 mg three times per day during weeks 1–12 of a 48-week treatment course and coadministered with pegylated interferon alpha plus ribavirin) and the trial control (matched placebo coadministered with pegylated interferon alpha plus ribavirin for 48 weeks)
Figure 2 Forest plot of indirect comparison of standard dose-duration treatments in naïve patients addressing sustained virologic response, relapse, and discontinuation.
Figure 4 Forest plot of indirect comparison of response-guided therapy treatments in naïve patients addressing sustained virologic response, relapse, and discontinuation.
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