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Terminated Phase 2 Interventional Results available

A Study to Evaluate Efficacy and Safety of Deucravacitinib in Participants With Alopecia Areata

ClinicalTrials.gov ID: NCT05556265

Public ClinicalTrials.gov record NCT05556265. 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.

ClinicalTrials.gov public records Last synced Nov 11, 2026, 3:24 AM EST

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Official title

A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 2 Study to Evaluate Clinical Efficacy and Safety of Deucravacitinib (BMS-986165) in Participants With Alopecia Areata

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the efficacy of deucravacitinib versus placebo at Week 24 and safety and tolerability of deucravacitinib versus placebo in adults with alopecia areata.

Study identification

NCT ID
NCT05556265
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
94 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 65 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
Nov 8, 2022 (Actual)
Primary completion
Jan 6, 2024 (Actual)
Completion
May 16, 2024 (Actual)
Last update posted
May 31, 2025

2022 – 2024

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Local Institution - 0016 Santa Monica California 90404-2120 —
Local Institution - 0036 New Haven Connecticut 06510 —
Local Institution - 0018 Tampa Florida 33624-2038 —
Local Institution - 0023 Clinton Township Michigan 48038-1137 —
Local Institution - 0024 New York New York 10029-6501 —
Local Institution - 0019 Chapel Hill North Carolina 27516-4061 —
Local Institution - 0011 Portland Oregon 97201-5134 —
Local Institution - 0032 Pittsburgh Pennsylvania 15213-3403 —
Local Institution - 0012 Austin Texas 78759 —
Local Institution - 0013 Houston Texas 77004-8098 —
Local Institution - 0014 San Antonio Texas 78213-2250 —
Local Institution - 0017 South Jordan Utah 84095 —

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05556265, 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 May 31, 2025 · Synced Nov 11, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05556265 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →