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Study details
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A Study to Evaluate the Efficacy, Safety, and Drug Levels of Deucravacitinib (BMS-986165) in Adolescent Participants With Moderate to Severe Plaque Psoriasis

Bristol-Myers Squibb
NCT IDNCT06979453ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

366

Study length

about 8.7 years

Ages

12–17

Locations

39 sites in AL, AZ, CA +19

What this study is about

This trial is testing a treatment called Deucravacitinib in adolescents with moderate to severe plaque psoriasis. The goal is to see if this treatment helps improve the condition, and also to understand its safety and how it affects drug levels in the body.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Placebo
  • 2.Take Deucravacitinib

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

deucravacitinib

Drug routes

oral (Oral Tablet)

Endpoints

Secondary: Body weight, Change from baseline in Children's Dermatology Life Quality Index (CDLQI) score, Change from baseline in PASI, Change from baseline in body surface area (BSA) involvement, Change from baseline in worst itch numeric rating scale (WI-NRS), Height, Number of participants achieving ≥ 4 improvement from baseline in the WI-NRS score (in participants with baseline score ≥ 4), Number of participants with serious adverse events

Body systems

Dermatology