Local Institution
Melbourne, Victoria, 3004, Australia
NCT Number: NCT00979368
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics following single oral doses of BMS-816336 in healthy male subjects.
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Notify Me18 year–55 year
Male
Interventional
Phase 1
Melbourne, Victoria, 3004, Australia
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Suspension, Oral, 15 mg Active, Once on Day 1 only, 4 days
Suspension, Oral, 0 mg, Once on Day 1 only, 4 days
Time frame: Within 72 hours following dosing
Time frame: During 72 hours following dosing
Bristol-Myers Squibb
Industry
Randomized, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BMS-816336 in Healthy Male Subjects
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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