57
Participants
Start Date
September 30, 2011
Primary Completion Date
May 31, 2012
Study Completion Date
May 31, 2012
BMS-820836
Tablets, Oral, 0.5 mg, Once daily, 14 days
BMS-820836
Tablets, Oral, 1 mg, Once daily, 14 days
BMS-820836
Tablets, Oral, 2 mg, Once daily, 14 days
Placebo matching BMS-820836
Tablets, Oral, 0 mg, Once daily, 14 days
BMS-820836
Tablets, Oral, (initiated at 1 mg and dose escalated to the target dose of 2 mg), Once daily, 14 days
Local Institution, Taito-Ku
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY