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Completed Phase 4 Interventional Results available

Efficacy and Safety of Deucravacitinib Versus Placebo in Participants With Moderate-to-severe Scalp Psoriasis

ClinicalTrials.gov ID: NCT05478499

Public ClinicalTrials.gov record NCT05478499. 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 Oct 27, 2026, 3:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3B/4, Multicenter, Randomized, Double-blind Placebo-controlled Study to Evaluate the Efficacy and Safety of Deucravacitinib in Participants With Moderate-to-severe Scalp Psoriasis (PSORIATYK SCALP)

Brief summary

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

The purpose of this study is to compare the efficacy and safety of deucravacitinib to placebo in participants with moderate-to-severe scalp psoriasis.

Study identification

NCT ID
NCT05478499
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
154 participants

Conditions and interventions

Conditions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
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
Oct 6, 2022 (Actual)
Primary completion
Jan 11, 2024 (Actual)
Completion
Oct 17, 2024 (Actual)
Last update posted
Oct 28, 2025

2022 – 2024

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
Local Institution - 0001 Hot Springs Arkansas 71913 —
Local Institution - 0007 Indianapolis Indiana 46256 —
Local Institution - 0041 Louisville Kentucky 40217 —
Local Institution - 0022 Rockville Maryland 20850 —
Local Institution - 0008 Beverly Massachusetts 01915 —
Local Institution - 0047 Bloomfield Hills Michigan 48302 —
Local Institution - 0002 New Brighton Minnesota 55432 —
Local Institution - 0049 East Windsor New Jersey 08520 —
Local Institution - 0051 Kew Gardens New York 11415 —
Local Institution - 0003 Portland Oregon 97201 —
Local Institution - 0005 Pittsburgh Pennsylvania 15213 —
Local Institution - 0033 Houston Texas 77004 —
Local Institution - 0004 San Antonio Texas 78229 —
Local Institution - 0006 Norfolk Virginia 23502 —

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05478499, 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 Oct 28, 2025 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05478499 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →