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The purpose of this study is to evaluate the safety, pharmacokinetics, and target engagement of BMS-986142 in healthy subjects.
Allocation: Randomized Controlled Trial (SAD/MAD) Masking: Double-Blind (SAD/MAD)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1: BMS-986142 or placebo | Experimental | BMS-986142 or placebo Single dose oral Solution or spray dried dispersion as specified |
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| Group 2: BMS-986142 or placebo | Experimental | BMS-986142 or placebo Multiple dose oral Solution as specified |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BMS-986142 | Drug |
| ||
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Primary safety endpoint is based on the incidence, potential significance, and clinical importance of adverse events after single dose of BMS-986142 | Single Ascending Dose(SAD) within 8 days | |
| Primary safety endpoint is based on the incidence, potential significance, and clinical importance of adverse events after multiple doses of BMS-986142 | Multiple Ascending Dose (MAD) within 19 days |
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For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Wcct Global, Llc | Cypress | California | 90630 | United States |
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| Drug |
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