The primary purpose of this study is to evaluate the safety profile and tolerability of single oral doses of BMS-650032 in subjects with chronic hepatitis C infection
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
24
Oral, Once daily, Single Dose
West Coast Clinical Trials, Llc
Cypress, California, United States
Orlando Clinical Research Center
Orlando, Florida, United States
Parexel International Corporation
Baltimore, Maryland, United States
Mayo Clinic
Rochester, Minnesota, United States
Safety Outcome Measures
Time frame: Safety and tolerability assessments will be performed for a period of 7 days after administration of a single dose
Pharmacokinetic Measures
Time frame: Pharmacokinetic assessments will be done for a period of 72 hours following administration of a single oral dose
Pharmacodynamic Measures
Time frame: Antiviral activity will be assessed by the magnitude and rate of change in plasma HCV RNA levels for a period of 7 days after dosing
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Alamo Medical Research
San Antonio, Texas, United States