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This is an investigational study of Cyclosporine on the experimental medication BMS-986165 in healthy male participants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| BMS-986165 and cyclosporine | Experimental | BMS-986165 and cyclosporine administered orally |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BMS-986165 | Drug | Specified dose on specified days |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Maximum concentration (Cmax) | 24 hours | |
| Area under the concentration vs time curve from time zero to 24 hours post dose (AUC[0-24]) | 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events (AEs) | Up to 20 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 |
|---|---|---|---|---|---|---|
| PRA Health Sciences | Salt Lake City | Utah | 84124 | United States |
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| Label | URL |
|---|---|
| BMS Clinical Trial Patient Recruiting | View source |
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| ID | Term |
|---|---|
| D011565 | Psoriasis |
| ID | Term |
|---|---|
| D017444 | Skin Diseases, Papulosquamous |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| C000628674 | deucravacitinib |
| D016572 | Cyclosporine |
| ID | Term |
|---|---|
| D003524 | Cyclosporins |
| D010456 | Peptides, Cyclic |
| D047028 | Macrocyclic Compounds |
| D011083 | Polycyclic Compounds |
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| Cyclosporine |
| Drug |
Specified dose on specified days |
|
| D010455 |
| Peptides |
| D000602 | Amino Acids, Peptides, and Proteins |