Overview
A Single and Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics, and Target Engagement of BMS-986147 in Healthy Subjects
Status:
Completed
Completed
Trial end date:
2014-11-01
2014-11-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is the first clinical study with the BMS-986147 compound in healthy subjects. The purpose of this study is to guide the dose range and dose frequency for future studies with BMS-986147 and will provide guidelines for selection of a potentially effective dose in patients.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Bristol-Myers Squibb
Criteria
For more information regarding BMS clinical trial participation, please visitwww.BMSStudyConnect.com
Inclusion Criteria:
- Healthy men and women, ages 18 to 45 years
- Subjects must not have clinically significant deviation from normal: medical history,
physical examination, ECGs and laboratory evaluations
- Women of child bearing potential are eligible for enrollment.
- Women must have a negative pregnancy test
Exclusion Criteria:
- Evidence of organ dysfunction
- Any significant acute or chronic medical illness
- Inability to: tolerate oral medications, be venipunctured