Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

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

NCT06979453 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the efficacy, safety, and drug levels of Deucravacitinib (BMS-986165) in adolescent participants with moderate to severe plaque psoriasis

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Deucravacitinib

Study Locations (20)

California

  • Local Institution - 0025 — Fountain Valley
  • Center For Dermatology Clinical Research, Inc. — Fremont
  • Dermatology Research Associates — Los Angeles
  • Northridge Clinical Trials — Northridge
  • Local Institution - 0077 — Sacramento
  • Golden State Dermatology - Walnut Creek - Ygnacio Valley Road — Walnut Creek

Florida

  • Local Institution - 0021 — Clearwater
  • Life Clinical Trials — Margate
  • Skin Research of South Florida — Miami
  • Wellness Clinical Research — Miami Lakes
  • Palm Harbor Dermatology PA d/b/a TrueBlue Clinical Research — Tampa

Alabama

  • Local Institution - 0261 — Birmingham
  • Local Institution - 0041 — Birmingham

Georgia

  • Dermatology Affiliates Research Institute — Atlanta
  • Advanced Medical Research, PC. — Sandy Springs

Arizona

  • Local Institution - 0053 — Phoenix

Colorado

  • Paradigm Clinical Research, LLC — Wheat Ridge

Indiana

  • Dawes Fretzin Clinical Research Group, LLC — Indianapolis

Kentucky

  • Local Institution - 0262 — Murray

Trial Details

FieldValue
Enrollment Target 366 participants
Start Date 2025-12-03
Est. Completion 2034-08-12
Phase Phase 3

Sponsor

Bristol-Myers Squibb

504 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06979453

The ClinicalTrials.gov registry entry for NCT06979453 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 366 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Plaque Psoriasis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06979453 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06979453 about?

NCT06979453 is a clinical study titled "A Study to Evaluate the Efficacy, Safety, and Drug Levels of Deucravacitinib (BMS-986165) in Adolescent Participants With Moderate to Severe Plaque Psoriasis". The purpose of this study is to evaluate the efficacy, safety, and drug levels of Deucravacitinib (BMS-986165) in adolescent participants with moderate to severe plaque psoriasis

What is the current status of trial NCT06979453?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 366 participants. The study started on 2025-12-03. Estimated completion is 2034-08-12.

What conditions does trial NCT06979453 study?

This clinical trial studies the following conditions: Plaque Psoriasis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06979453?

The interventions under investigation include: Placebo (OTHER), Deucravacitinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06979453?

This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06979453 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial