ClinicalTrials.gov record
Terminated Phase 4 Interventional Results available

A Study to Evaluate Effectiveness and Safety of Deucravacitinib in Participants With Non-Pustular Palmoplantar and Genital Psoriasis

ClinicalTrials.gov ID: NCT06042920

Public ClinicalTrials.gov record NCT06042920. 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 May 19, 2026, 8:32 AM 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 4, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Deucravacitinib in Participants With Non-Pustular PalmoPlantar and Genital Psoriasis (Psoriatyk Special Sites)

Study identification

NCT ID
NCT06042920
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
130 participants

Conditions and interventions

Interventions

  • Deucravacitinib Drug
  • Placebo Drug

Drug

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 8, 2023
Primary completion
Apr 24, 2025
Completion
Apr 24, 2025
Last update posted
Apr 16, 2026

2023 – 2025

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Local Institution - 0050 Phoenix Arizona 85006-2722
Local Institution - 0015 Fountain Valley California 92708
Local Institution - 0009 Los Angeles California 90045-3606
Local Institution - 0004 Santa Monica California 90404
Local Institution - 0057 Skokie Illinois 60077-1049
Local Institution - 0052 Indianapolis Indiana 46250
Local Institution - 0053 Plainfield Indiana 46168-2792
Local Institution - 0029 Rockville Maryland 20850-6243
Local Institution - 0012 Detroit Michigan 48202-3141
Local Institution - 0005 East Windsor New Jersey 08520-2505
Local Institution - 0002 New York New York 10003
Local Institution - 0008 New York New York 10075
Local Institution - 0062 New York New York 10128
Local Institution - 0001 Winston-Salem North Carolina 27157
Local Institution - 0066 Boardman Ohio 44512
Local Institution - 0055 Mayfield Heights Ohio 44124-4005
Local Institution - 0056 Pittsburgh Pennsylvania 15213-3403
Local Institution - 0010 Houston Texas 77004
Local Institution - 0007 Norfolk Virginia 23502-3933
Local Institution - 0033 Mill Creek Washington 98012-1797

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06042920, 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 Apr 16, 2026 · Synced May 19, 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 protocol, eligibility criteria, and contact information for NCT06042920 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →