Overview
Safety Study of BMS-986165 in Healthy Subjects and to Treat Psoriasis
Status:
Completed
Completed
Trial end date:
2016-11-01
2016-11-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to establish if BMS-986165 is safe and effective at treating autoimmune diseases. BMS-986165 which has shown some promise in preclinical studies for inhibiting autoimmune conditions. This study will be the first time this drug is given to humans, and will be conducted entirely in healthy subjects. It will be run in 4 Parts. Part A will investigate single oral doses of drug. Part B will investigate giving the drug daily for 14 days. Part C will investigate daily doses for 14 days in healthy volunteers with Japanese decent. Part D will investigate whether food, stomach acidity or giving the drug in a capsule makes a difference to the safety and potential use of this drug.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Bristol-Myers SquibbTreatments:
BMS-986165
Famotidine
Interferon alpha-2
Interferon-alpha
Interferons
Criteria
For more information regarding BMS clinical trial participation, please visitwww.BMSStudyConnect.com
Inclusion Criteria:
- Healthy Male and Female participants
- 18 to 50 years of age (Parts A-D)
Exclusion Criteria:
- Participants that had recent infections
- Participants with low blood pressure or increased heart rate
- Participants with any chronic health related problems
- Participants with active cancer within the last 5 years
- Participants with any other major medical illness