Short Term Treatment With BI 201335, Peginterferon-alpha 2a and Ribavirin in Hepatitis c Virus Genotype-1 Treatment-naïve Patients (SILEN-C3)

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

To compare the antiviral efficacy and safety of a 12-week with a 24-week treatment of BI 201335 at a dose of 120 mg once daily, with a 24-week background of pegylated interferon-alpha 2a (PegIFN) plus ribavirin (RBV), in treatment-naïve patients infected with hepatitis C virus (HCV) genotype 1

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Boehringer Ingelheim
• Treatments: Interferon-alpha; Interferons; Peginterferon alfa-2a; Ribavirin

Criteria

Inclusion criteria:

1. Chronic hepatitis C infection of genotype 1

2. Therapy-naïve to interferon, pegylated interferon, and ribavirin

3. HCV viral load > 100.000 IU/ml at screening

4. Liver biopsy or fibroscan within two years prior to screening that provides evidence of any degree of fibrosis or cirrhosis

5. Normal retinal finding on fundoscopy within 6 months prior to Day 1

6. Age 18 to 70 years

Exclusion criteria:

1. HCV of mixed genotype (1/2, 1/3, and 1/4) .

2. Patients who have been previously treated with at least one dose of any protease inhibitor

3. Evidence of liver disease due to causes other than chronic HCV infection

4. Positive for HIV-1 or HIV-2 antibodies

5. Hepatitis B virus (HBV) infection

6. Decompensated liver disease, or history of decompensated liver disease

7. Active malignancy or history of malignancy within the last 5 years

8. History of alcohol or drug abuse (except cannabis) within the past 12 months.

9. Body Mass Index < 18 or > 35 kg/m2.

10. Usage of any investigational drugs within 30 days prior to enrolment

11. Alpha fetoprotein value >100ng/mL at screening;

12. Total bilirubin > 1.5 x ULN with ratio of direct/indirect > 1.

13. ALT or AST level > 10 x ULN