68
Participants
Start Date
July 31, 2008
Primary Completion Date
April 30, 2009
Study Completion Date
April 30, 2009
BMS-820836
Oral Solution, Oral, 0.025 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 0.1 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 0.25 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 0.5 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 1 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 2 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 3 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 5 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 8 mg, single dose, one dose
Placebo
Oral Solution, Oral, 0 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 3 mg, single dose, one dose
BMS-820836
Oral Solution, Oral, 0.5 mg, single dose, one dose
Local Institution, Toronto
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY