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| ID | Type | Description | Link |
|---|---|---|---|
| 2017-004136-10 | EudraCT Number |
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The purpose of this study is to investigate experimental medication BMS-986278 given to healthy participants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Single Ascending Dose | Experimental | BMS-986278 or placebo |
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| Multiple Ascending Dose | Experimental | BMS-986278 or placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BMS-986278 | Drug | Specified dose on specified days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants experiencing adverse events (AE), serious adverse events (SAE), death, or an AE leading to study discontinuation | Up to 30 days | |
| Number of participants with potentially clinically significant changes in ECG parameters, vital signs, clinical laboratory parameters, or physical examinations | Up to 30 days |
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For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
Exclusion Criteria:
Other protocol defined inclusion/exclusion criteria could apply
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Local Institution | Groningen | 9728 NZ | Netherlands | |||
| Local Institution |
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| Label | URL |
|---|---|
| BMS Clinical Trial Information | View source |
| BMS Clinical Trial Patient Recruiting | View source |
| Investigator Inquiry Form |
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| Placebo | Other | Specified dose on specified days |
|
| London |
| SE1 1YR |
| United Kingdom |
| FDA Safety Alerts and Recalls | View source |