Deucravacitinib-TNFi Combination Therapy for Difficult-to-Control Psoriatic Disease

Part of paid clinical trials in Dallas, Texas.

Sponsor
University of Texas Southwestern Medical Center
Study ID
NCT07280702
Phase
PHASE4
Status
Recruiting

Conditions

  • Psoriatic Arthritis (PsA)

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Deucravacitinib — DRUG
    Drug will be administered in tablet form.
  • Placebo — DRUG
    Drug will be administered in tablet form.

Study Details

The purpose of this research study is to determine the effectiveness of adding deucravacitinib to the participant's current Psoriatic Arthritis (PsA) treatment to see if it improves their symptoms and quality of life. This study is exploring a new treatment approach that may help improve control of psoriatic disease by targeting different parts of the disease process. By combining therapies that work together, the goal is to offer better symptom relief with fewer or more manageable side effects than some current treatments.

Key Dates

First listed
Dec 12, 2025
Start date
Jun 16, 2026
Status verified
Aug 2026
Primary completion
Dec 15, 2027
Completion
Dec 15, 2027

Study Design

Enrollment
128 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: established standard of care anti-TNF plus deucravacitinib
    Deucravacitinib will be administered in tablet form. Anti-TNF will be administered by injection.
  • Placebo Comparator: established standard of care anti-TNF plus placebo
    Placebo will be administered in tablet form. Anti-TNF will be administered by injection.

Primary Outcome Measure

Proportion of patients achieving a novel composite endpoint of BSA </= 1 AND SJC </= 1) OR (BSA </= 1 AND TJC </= 1) at 24 weeks [ Time Frame: 24 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UT Southwestern Medical CenterDallasTexas75390
Joseph F Merola, MD MMSc
917-671-8192
Aleuna Lee, PhD, CCRC
214-645-8968

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