Volume 141, Issue 6, Pages 2047-2055 (December 2011) Efficacy of the Protease Inhibitor BI 201335, Polymerase Inhibitor BI 207127, and Ribavirin in Patients With Chronic HCV Infection Stefan Zeuzem, Tarik Asselah, Peter Angus, Jean–Pierre Zarski, Dominique Larrey, Beat Müllhaupt, Ed Gane, Marcus Schuchmann, Ansgar Lohse, Stanislas Pol, Jean–Pierre Bronowicki, Stuart Roberts, Keikawus Arasteh, Fabien Zoulim, Markus Heim, Jerry O. Stern, George Kukolj, Gerhard Nehmiz, Carla Haefner, Wulf Otto Boecher Gastroenterology Volume 141, Issue 6, Pages 2047-2055 (December 2011) DOI: 10.1053/j.gastro.2011.08.051 Copyright © 2011 AGA Institute Terms and Conditions
Figure 1 Trial schema. eRVR, extended rapid virologic response (HCV RNA level ≤25 IU/mL at week 4, and HCV RNA undetectable from weeks 5 to 18); QD, once daily; TID, 3 times daily. Gastroenterology 2011 141, 2047-2055DOI: (10.1053/j.gastro.2011.08.051) Copyright © 2011 AGA Institute Terms and Conditions
Figure 2 Patient disposition. Gastroenterology 2011 141, 2047-2055DOI: (10.1053/j.gastro.2011.08.051) Copyright © 2011 AGA Institute Terms and Conditions
Figure 3 Absolute HCV RNA level from baseline to day 29 for individual patients in (A) the BI 207127 400 mg dose group and (B) the BI 207127 600 mg dose group. *Patient with virologic breakthrough observed during treatment at day 22. **Patient with an increase in HCV RNA from nadir of 0.7 log10 IU/mL. LLOD, 17 IU/mL; LLOQ, 25 IU/mL. Gastroenterology 2011 141, 2047-2055DOI: (10.1053/j.gastro.2011.08.051) Copyright © 2011 AGA Institute Terms and Conditions