Study to assess the antiviral efficacy, pharmacokinetics, and tolerability of 200 mg BILN 2061 ZW in a polyethylene glycol 400 (PEG 400: ethanol) drinking solution given orally for two days bid to patients with cirrhosis and chronic Hepatitis C Virus (HCV) infection
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
10
Virus load (VL) as determined by number of copies of HCV mRNA per ml serum
Cobas Amplicor HCV Monitor v 2.0 (HCM-2.0, Roche Diagnostics)
Time frame: up to day 14
Number of patients with relevant drug-induced changes in alanine aminotransferase (ALT)
Time frame: up to day 14
Number of patients with relevant drug-induced changes in aspartate aminotransferase (AST)
Time frame: up to day 14
Number of patients with relevant drug-induced changes in vital signs (pulse rate, systolic and diastolic blood pressure)
Time frame: up to day 14
Number of patients with relevant drug-induced changes in electrocardiography (ECG)
Time frame: up to day 14
Number of patients with relevant drug-induced changes in routine laboratory tests
Time frame: up to day 14
Number of patients with adverse events
Time frame: up to 35 days
Maximum concentration in plasma after a single dose administration (Cmax)
Time frame: up to day 4
Area under the plasma concentration-time curve from t = 0 to t = .τ rate (AUC0-τ)
Time frame: up to day 4
Time to reach Cmax following a single dose administration (tmax)
Time frame: up to day 4
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Total oral clearance of drug from plasma after oral administration, divided by F (CL/F)
Time frame: up to day 4
Apparent volume of distribution during the terminal elimination phase (Vz/F)
Time frame: up to day 4
Assessment of tolerability by investigator on a 4-point scale
Time frame: day 3