Table G.

Adjusted indirect comparison of the proportion of patients achieving a sustained virologic response, relapsing to treatment, or discontinuing treatment at any point in a 48-week treatment course using boceprevir or telaprevir

	Boceprevir	Telaprevir	Relative risk (95% CI)	P value
Sustained virologic response
Patients
Naïve	1.65 (1.43–1.91)	1.64 (1.50–1.79)	1.01 (0.85–1.19)	0.94
Experienced	2.98 (2.29–3.87)	3.88 (3.05–4.94)	0.77 (0.54–1.10)	0.15
Relapse
Patients
Naïve	0.42 (0.28–0.61)	0.30 (0.22–0.39)	1.40 (0.86–2.28)	0.18
Experienced	0.40 (0.26–0.62)	0.22 (0.17–0.29)	1.82 (1.09–3.03)	0.02
Discontinuation
Patients
Naïve	0.75 (0.64–0.88)	0.75 (0.45–1.23)	1.00 (0.59–1.69)	1.00
Experienced	0.52 (0.44–0.60)	0.60 (0.47–0.77)	0.87 (0.65–1.16)	0.34

Abbreviation: CI, confidence interval.