The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics following single oral doses of BMS-816336 in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
TRIPLE
Enrollment
40
Suspension, Oral, 15 mg Active, Once on Day 1 only, 4 days
Suspension, Oral, 60 mg Active, Once on Day 1 only, 4 days
Suspension, Oral, 180 mg Active, Once on Day 1 only, 4 days
Local Institution
Melbourne, Victoria, Australia
Exposure to the investigational drug will be measured to assess safety and tolerability
Time frame: Within 72 hours following dosing
To assess the single dose Pharmacokinetics of BMS-816336
Time frame: During 72 hours following dosing
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Suspension, Oral, 450 mg Active, Once on Day 1 only, 4 days
Suspension, Oral, 900 mg Active, Once on Day 1 only, 4 days
Suspension, Oral, 0 mg, Once on Day 1 only, 4 days