At a glance
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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)
In Brief
A Phase 2 clinical trial evaluating Deucravacitinib and Placebo for Lupus Erythematosus, Discoid and Lupus Erythematosus, Subacute Cutaneous. Active but no longer recruiting, targeting 74 participants across 41 sites in 8 countries.
Detailed Summary
The purpose of this study is to assess the safety, efficacy, and tolerability of deucravacitinib (BMS-986165) compared with placebo in participants with active discoid and/or subacute cutaneous lupus erythematosus (DLE/SCLE). This study will also assess if deucravacitinib 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.
Study Details
Timeline
Interventions
Specified dose on specified days
Specified dose on specified days