1. Hepatitis web study Hepatitis web study 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + RBV in GT1 SAPPHIRE-I Phase 3 Treatment Naïve Feld JJ, et al. N Engl J Med. 2014;370:1594-1603.

2. Hepatitis web study Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Design

3. Hepatitis web study Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Study Regimens Group A N = 473 3D + Ribavirin Placebo SVR12 3D + Ribavirin SVR12 Double blind Open label (data pending) Group B N = 158 Week 0361224 3D = Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir Drug Dosing 3D = Paritaprevir-Ritonavir-Ombitasvir (150/100/25 mg once daily) + Dasabuvir: 250 mg twice daily Ribavirin (RBV): weight-based and divided bid (1000 mg/day if < 75kg or 1200 mg/day if ≥ 75kg)

4. Hepatitis web study Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Baseline Characteristics Baseline Characteristic Group A (n=473) Group B (n=158) Age (years), Mean49.451.2 Male sex %57.346.2 Race (%) White Black Other 90.5 5.5 4.0 91.1 5.1 3.8 Body Mass Index (Mean)25.726.2 HCV genotype (%) 1a 1b 68.1 31.9 66.5 33.5 IL28B CC genotype, (%)30.431.6 HCV RNA, log 10 IU/ml6.406.47 Fibrosis score ≥ F223.326.6

5. Hepatitis web study 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Results SAPPHIRE-I: SVR12 in Group A (3D + Ribavirin) Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 455/473307/322148/151

6. Hepatitis web study Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Adverse Events During Double-Blind Phase NUTRINO: SVR 12 by Liver Disease Event Group A = 3D + RBV (n=473) Group B = Placebo (n=158) Any adverse event (%)87.573.4 Any adverse event leading to discontinuation of study drug (%) 0.6 Any serious adverse event2.10 Grade 3 or 4 lab abnormality (%) Alanine aminotransferase0.94.4 Aspartate aminotransferase0.61.9 Alkaline phosphatase00 Total bilirubin2.80 Hemoglobin00

7. Hepatitis web study Source: Feld JJ, et al. N Engl J Med. 2014;370:1594-1603. 3D (Paritaprevir-Ritonavir-Ombitasvir + Dasabuvir) + Ribavirin in GT1 SAPPHIRE-I Study: Conclusions Conclusions: “In previously untreated patients with HCV genotype 1 infection and no cirrhosis, a 12-week multitargeted regimen of ABT- 450/r–ombitasvir and dasabuvir with ribavirin was highly effective and was associated with a low rate of treatment discontinuation.” Note: ABT-450/r = Paritaprevir-Ritonavir

8. Hepatitis web study Hepatitis web study This slide deck is from the University of Washington’s Hepatitis C Online and Hepatitis Web Study projects. Hepatitis C Online www.hepatitisc.uw.edu www.hepatitisc.uw.edu Hepatitis Web Study http://depts.washington.edu/hepstudy/ http://depts.washington.edu/hepstudy/ Funded by a grant from the Centers for Disease Control and Prevention. This slide deck is from the University of Washington’s Hepatitis C Online and Hepatitis Web Study projects. Hepatitis C Online www.hepatitisc.uw.edu www.hepatitisc.uw.edu Hepatitis Web Study http://depts.washington.edu/hepstudy/ http://depts.washington.edu/hepstudy/ Funded by a grant from the Centers for Disease Control and Prevention.