A Caspase Inhibitor in Chronic Hepatitis C (HCV) Patients
Hepatitis C, Chronic
About this trial
This is an interventional treatment trial for Hepatitis C, Chronic
Eligibility Criteria
Inclusion Criteria: Chronic hepatitis C infection Unsuccessful prior HCV treatment Liver impairment (either AST or ALT 1.5-10.0 x ULN) Alpha-fetoprotein <= 50 ng/mL Adequate hematologic parameters Exclusion Criteria: Decompensated or severe liver disease Hepatocellular carcinoma HIV infection Co-infection with hepatitis B virus (HBV) Renal impairment Pancreatitis Use of illicit or drugs of abuse History of alcohol abuse Presence of clinically significant cardiac arrhythmias If female, pregnant or lactating
Sites / Locations
- Mayo Clinic Hospital
- Scripps Clinic
- California Pacific Medical Center
- University of California, San Francisco
- University of Miami
- Indiana University School of Medicine
- Beth Israel Deaconness Medical Center
- Henry Ford Hospital
- The Mayo Clinic
- Mt. Sinai School of Medicine
- University of North Carolina
- Duke University Medical Center
- University of Cincinnati
- Metrohealth Medical Center
- Medical College of Virginia
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Active Comparator
Active Comparator
Active Comparator
Placebo
IDN-6556 5 mg twice a day (BID)
IDN-6556 25mg twice a day (BID)
IDN-6556 50 mg twice a day (BID)