The purpose of this study is to evaluate the effect of food on pharmacokinetics, safety and tolerability of an experimental Hepatitis C Virus (HCV) protease inhibitor with ritonavir in healthy volunteers.
This is an open-label, randomized, 2 cross-over period fasting and non-fasting study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
8
Site Reference ID/Investigator# 19421
Waukegan, Illinois, United States
Pharmacokinetics (blood draws, pre- and post-dose)
Time frame: 17 days
Safety and tolerability (ECGs, AEs, vitals, physical exams, routine labs)
Time frame: 30 days
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