Overview

Drug Drug Interaction Study Between BI 201335 and BI 207127 in Chronic Hepatitis C Infected Patients

Status:
Completed
Trial end date:
2014-10-01
Target enrollment:
0
Participant gender:
All
Summary
To evaluate the drug-drug interactions between BI 201335 and BI 207127 as well as their combined effect on CYP probe drug substrates and on tenofovir and raltegravir in treatment naive or prior treatment relapse patients with chronic hepatitis C infection.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Boehringer Ingelheim
Treatments:
Caffeine
Interferons
Midazolam
Protease Inhibitors
Ribavirin
Tenofovir
Tolbutamide
Criteria
Inclusion criteria:

1. Chronic hepatitis C genotype 1 infection, diagnosed at least 6 months prior to
screening

2. Treatment naive or confirmed prior treatment relapse or partial response following
treatment with interferon and ribavirin

3. Age 18 to 70 years

4. HCV RNA (Hepatitis C Virus RiboNucleic Acid) = 1,000 IU/mL at screening

5. Liver biopsy or fibroscan to exclude cirrhosis

Exclusion criteria:

1. Hepatitis C Virus (HCV) infection of mixed genotype; Hepatitis B Virus (HBV) or Human
Immunodeficiency Virus (HIV) co-infection

2. Evidence of acute or chronic liver disease due to causes other than chronic HCV
infection,

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

4. Body weight < 40 or > 125 kg,

5. Clinical evidence of significant or unstable cardiovascular disease, chronic pulmonary
disease, history or evidence of retinopathy or clinically significant ophthalmological
disorder

6. Pre-existing psychiatric condition that could interfere with the subject's
participation in and completion of the study

7. Laboratory parameters disorders (thalassemia major, sickle cell anemia or glucose 6
phosphate dehydrogenase deficit)

8. Hemoglobin < 12 g/dL for women and < 13 g/dL for men

9. Patients who have been previously treated with at least one dose of any antiviral or
immunomodulatory drug other than interferon alfa or ribavirin for acute or chronic HCV
infection