A Study to Evaluate Efficacy and Safety of Deucravacitinib in Participants With Active Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE)
Public ClinicalTrials.gov record NCT04857034. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Efficacy and Safety of Deucravacitinib (BMS-986165) in Participants With Active Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE)
Study identification
- NCT ID
- NCT04857034
- Recruitment status
- Active, not recruiting
- Study type
- Interventional
- Phase
- Phase 2
- Lead sponsor
- Bristol-Myers Squibb
- Industry
- Enrollment
- 74 participants
Conditions and interventions
Interventions
- Deucravacitinib Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years to 75 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jul 11, 2021
- Primary completion
- Aug 21, 2024
- Completion
- Feb 27, 2028
- Last update posted
- Sep 9, 2025
2021 – 2028
United States locations
- U.S. sites
- 12
- U.S. states
- 11
- U.S. cities
- 12
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Local Institution - 0077 | Scottsdale | Arizona | 85259 | — |
| Local Institution - 0076 | Irvine | California | 92697 | — |
| Local Institution - 0046 | Los Angeles | California | 90045 | — |
| Local Institution - 0073 | Farmington | Connecticut | 06030 | — |
| Local Institution - 0082 | Orlando | Florida | 32827 | — |
| Local Institution - 0060 | Ann Arbor | Michigan | 48109 | — |
| Local Institution - 0059 | St Louis | Missouri | 63108 | — |
| Local Institution - 0037 | New York | New York | 10029 | — |
| Local Institution - 0065 | Durham | North Carolina | 27713 | — |
| Local Institution - 0067 | Columbus | Ohio | 43215 | — |
| Local Institution - 0026 | Oklahoma City | Oklahoma | 73104 | — |
| Local Institution - 0054 | Charleston | South Carolina | 29407 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04857034, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Sep 9, 2025 · Synced Jul 22, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04857034 live on ClinicalTrials.gov.