Efficacy and Safety Study of Simeprevir in Combination With Sofosbuvir in Participants With Genotype 1 Chronic Hepatitis C Virus Infection and Cirrhosis

• Status: Completed
• Trial end date: 2015-04-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of the study is to investigate the efficacy and safety of 12 weeks of simeprevir (150 mg qd) in combination with sofosbuvir (400 mg qd) in chronic hepatitis C virus (HCV) genotype 1 infected men and women with cirrhosis who are HCV treatment-naïve or treatment-experienced.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Janssen Infectious Diseases BVBA
• Treatments: Simeprevir; Sofosbuvir

Criteria

Inclusion Criteria:

• Hepatitis C virus (HCV) genotype 1 infection (confirmed at screening).

• HCV ribonucleic acid (RNA) greater than 10,000 IU/mL at screening

• Treatment-experienced participants must have at least 1 documented previous course of interferon-based regimen with or without ribavirin

• Participants must have an hepatic imaging procedure (ultrasound, computerized tomography scan or magnetic resonance imaging scan) within 6 months prior to the screening visit (or between screening and Day 1) with no findings suspicious for hepatocellular carcinoma

• Participant must be willing and able to comply with the protocol requirements

• Participants with liver cirrhosis

Exclusion Criteria:

• Evidence of clinical hepatic decompensation (history or current evidence of ascites, bleeding varices or hepatic encephalopathy)

• Infection/co-infection with HCV non-genotype 1

• Co-infection with human immunodeficiency virus (HIV) type 1 or type 2 (HIV-1 or HIV-2) (positive HIV-1 or HIV-2 antibodies test at screening)

• Co-infection with hepatitis B virus (hepatitis B-surface-antigen positive)

• Previously been treated with any direct acting anti-HCV agent (approved or investigational) for chronic HCV infection