A Study to Continue the Administration of Deucravacitinib in Participants With Systemic Lupus Erythematosus (SLE) or Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE) Who Have Completed Study IM011074 or Study IM011132
Part of paid clinical trials in Farmington, Connecticut.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT06875960
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE)
- Systemic Lupus Erythematosus (SLE)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- BMS-986165 — DRUGSpecified dose on specified days
Study Details
The purpose of this study is to allow the continued administration of Deucravacitinib in participants with Systemic Lupus Erythematosus (SLE) or Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE) who have completed study IM011074 or Study IM011132
Key Dates
- Start date
- Feb 24, 2026
- Status verified
- Mar 2026
- Primary completion
- Dec 1, 2026
- Completion
- Dec 1, 2026
Study Design
- Enrollment
- 35 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Administration of BMS-986165
Primary Outcome Measure
Number of participants treated with BMS-986165 [ Time Frame: Up to 2 years ]
Central Contacts
- BMS Clinical Trials Contact Center www.BMSClinicalTrials.com855-907-3286
- First line of the email MUST contain NCT # and Site #.
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 0001 | Farmington | Connecticut | 06030 | - |
| New York University School Of Medicine | New York | New York | 10155 | Amit Saxena, Site 0002 646-501-7387 |
| Oklahoma Medical Research Foundation | Oklahoma City | Oklahoma | 73104 | Cristina Arriens, Site 0004 405-271-7805 |
| Local Institution - 0003 | Jackson | Tennessee | 38305 | - |
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