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Clinical Trial Summary

The purpose of this study is to assess the safety, efficacy, and tolerability of BMS-986165 compared with placebo in participants with active discoid and/or subacute cutaneous lupus erythematosus (DLE/SCLE). This study will also assess if BMS-986165 is biologically active and potentially effective in the treatment of participants with moderate to severe DLE/SCLE with or without systemic lupus erythematosus (SLE) that is not well controlled with standard of care therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04857034
Study type Interventional
Source Bristol-Myers Squibb
Contact Recruiting sites have contact information. Please contact the si
Phone please email:
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date April 30, 2021
Completion date June 21, 2024

See also
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