Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
BMS-986165 Is broken down by the body through multiple pathways. This study Investigates the effect of blocking one pathway in the drug levels of BMS-986165 in health subjects.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm A: Single Dose (BMS-986165) | Experimental |
| |
| Arm B:Diflunisal and Single Dose (BMS-986165) | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BMS-986165 | Drug | Specified Dose on Specified Days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Maximum observed plasma concentration (Cmax) of BMS-986165 with and without UGT1A9 inhibitor | Up to 14 days | |
| Area under the plasma concentration-time AUC (0-T) of BMS-986165 with and without UGT1A9 inhibitor | up to 14 days | |
| Area under the plasma concentration-time curve from time zero extrapolated to infinite time AUC(INF) for BMS-986165 with and without UGT1A9 inhibitor | up to 14 days |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Adverse Events (AEs) | up to 48 days | |
| Number of participants with 12-lead Electrocardiogram (ECG) Abnormalities | up to 48 days | |
| Physical Examination of weight |
Not provided
For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com.
Inclusion Criteria:
Exclusion Criteria:
Other inclusion/exclusion criteria apply
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| PRA Health Sciences - Lenexa | Lenexa | Kansas | 66219 | United States |
Not provided
| Label | URL |
|---|---|
| BMS Clinical Trial Information | View source |
| BMS Clinical Trial Patient Recruiting | View source |
| Investigator Inquiry Form |
Not provided
Not provided
| ID | Term |
|---|---|
| C000628674 | deucravacitinib |
| D004061 | Diflunisal |
| ID | Term |
|---|---|
| D012459 | Salicylates |
| D062385 | Hydroxybenzoates |
| D010636 | Phenols |
| D001555 | Benzene Derivatives |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| diflunisal | Drug | Specified Dose on Specified Days |
|
| up to 48 days |
| Number of changes in blood pressure | up to 20 days |
| Number of changes in body temperature | up to 20 days |
| Number of changes in respiratory rate | up to 20 days |
| Number of clinical significant changes in lab assessment of blood serum | up to 48 days |
| Number of Clinically significant changes in assessment of blood | up to 20 days |
| Number of Clinically significant changes in lab assessment of urine | up to 20 days |
| FDA Safety Alerts and Recalls | View source |
| D006841 |
| Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |