24
Participants
Start Date
October 31, 2011
Primary Completion Date
November 30, 2011
Study Completion Date
November 30, 2011
INX-08189 50 mg
Study Day 0: Single 50 mg dose of INX-08189 in the morning
240 mg verapamil HCL ER
Study Days 6 to 11: 240 mg verapamil HCL ER once daily (QD) in the morning
50 mg dose of INX-08189 and 240 mg verapamil HCL ER
Study Day 12: Co-administration of single 50 mg dose of INX-08189 and 240 mg verapamil HCL ER in the morning
Prism Research, LLC, Saint Paul
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY