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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 227A<br />

39<br />

SVR12 results from the Phase II, open-label IMPACT<br />

study of simeprevir (SMV) in combination with daclatasvir<br />

(DCV) and sofosbuvir (SOF) in treatment-naïve and<br />

-experienced patients with chronic HCV genotype 1/4<br />

infection and decompensated liver disease<br />

Eric Lawitz 1 , Fred Poordad 1 , Julio A. Gutierrez 1 , Thomas Kakuda 2 ,<br />

Gaston Picchio 3 , Greet Beets 4 , Ann Vandevoorde 4 , Peter Van<br />

Remoortere 2 , Bert Jacquemyn 4 , Gemma Quinn 4 , Donghan Luo 2 ,<br />

Sivi Ouwerkerk-Mahadevan 5 , Leen Vijgen 4 , Veerle Van Eygen 4 ,<br />

Maria Beumont 5 ; 1 Texas Liver Institute, University of Texas Health<br />

Science Center, San Antonio, TX; 2 Janssen Research & Development,<br />

LLC, Titusville, NJ; 3 Infectious Diseases, Janssen Research<br />

& Development, San Francisco, CA; 4 Janssen Infectious Diseases<br />

BVBA, Beerse, Belgium; 5 Janssen Research & Development,<br />

Beerse, Belgium<br />

Purpose: The ongoing IMPACT study (NCT02262728)<br />

assessed SMV+DCV+SOF in HCV genotype (GT)1/4-infected<br />

patients (pts) with decompensated liver disease. We present<br />

sustained virologic response 12 weeks (w) after end of treatment<br />

(SVR12) from an interim analysis (IA). Methods: Treatment-naïve<br />

or PegIFN±RBV treatment-experienced cirrhotic<br />

adults with Child-Pugh (CP) score

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