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Looking for participantsPhase3

Long-Term Safety Study of Deucravacitinib Versus Ustekinumab in Participants With Psoriasis (PRAGMATYK)

Sponsor: Bristol-Myers Squibb

NCT ID: NCT07116967

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Deucravacitinib (drug), Ustekinumab (drug)
How long the study runs
Study runs about 64 months (dates as stated)
About the drug or intervention
Deucravacitinib — drug: Specified dose on specified days · Ustekinumab — drug: Specified dose on specified days
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
40 Years and over
Who
All
Number of participants
3,040
Started
2025-09-22
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for plaque psoriasis
  • • Phase3 - 3,040 participants
  • • A study to evaluate the long-term safety of Deucravacitinib versus Ustekinumab in participants with psoriasis

Who can take part?

  • • Ages 40 Years and over
  • • Diagnosed with plaque psoriasis

Where?

  • • London - Velocity Clinical Research - North London
  • • Southampton - University Hospital Southampton NHS Foundation Trust - Southampton General Hospital
  • • London - Barts Health NHS Trust
  • • Salford - Salford Care Organisation
  • • +4 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

A study to evaluate the long-term safety of Deucravacitinib versus Ustekinumab in participants with psoriasis

Plaque Psoriasis

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 40 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Participants with moderate-to-severe plaque psoriasis:
  • ✓Deemed by the Investigator to be a candidate for phototherapy or systemic treatment for psoriasis, including...
  • ✓Have at least 1 of the following cardiovascular risk factors:
  • ✓Current cigarette smoker
  • ✓Diagnosis of hypertension

Who cannot take part

  • ✗Participants must not have recent history of 1 of the following cardiovascular events: MI, stroke, or coronary...
  • ✗Other protocol define inclusion/exclusion criteria apply.
See the full criteria
Inclusion Criteria: * Participants with moderate-to-severe plaque psoriasis: 1. Deemed by the Investigator to be a candidate for phototherapy or systemic treatment for psoriasis, including ustekinumab; 2. Have at least 1 of the following cardiovascular risk factors: * Current cigarette smoker * Diagnosis of hypertension * Diagnosis of hyperlipidemia * Diabetes mellitus type 1 or 2 * History of one or more of the following cardiovascular events: Coronary intervention (PCI) or coronary artery bypass grafting (CABG), myocardial infarction (heart attack), cardiac arrest, hospitalization for unstable angina, acute coronary syndrome, stroke, or transient ischemic attack * Obesity * Family history of premature coronary heart disease or sudden death in a first-degree male relative younger than 55 years of age or in a first-degree female relative younger than 65 years of age. Exclusion Criteria: * Participants must not have recent history of 1 of the following cardiovascular events: MI, stroke, or coronary revascularization, or VTE within 90 days prior to Day 1. * Participants must not have unstable CVD, defined as a recent clinical cardiovascular event (eg, unstable angina, rapid atrial fibrillation), or a cardiac hospitalization (eg, pacemaker implantation, HF) within 90 days prior to Day 1. * Participants must not have evidence of active cancer or history of cancer (solid organ or hematologic malignancy including myelodysplastic syndrome) or lymphoproliferative disease within the previous 5 years (other than resected cutaneous basal cell or squamous cell carcinoma, or carcinoma of cervix in situ that has been treated with no evidence of recurrence). * Other protocol define inclusion/exclusion criteria apply.

Where Is This Study? (8 UK sites)

Velocity Clinical Research - North London

London N3 2JU, United Kingdom

Recruiting
Site contact (verified)
Kamran Hussain, Site 04422083786712

University Hospital Southampton NHS Foundation Trust - Southampton General Hospital

Southampton SO16 6YD, United Kingdom

Recruiting
Site contact (verified)
Michelle Oakford, Site 02744402381206594

Barts Health NHS Trust

London E11 1NR, United Kingdom

Recruiting
Site contact (verified)
Anthony Bewley, Site 0241+020853955226268

Salford Care Organisation

Salford M6 8HD, United Kingdom

Recruiting
Site contact (verified)
Richard Warren, Site 0297+4401617897373

Local Institution - 0499

Bristol BS82RA, United Kingdom

NOT_YET_RECRUITING

Velocity Clinical Research, High Wycombe

High Wycombe HP11 2QW, United Kingdom

Recruiting
Site contact (verified)
Judith Mackay, Site 0443+441494506236

NHS Fife - Victoria Hospital

Kirkcaldy KY2 5AH, United Kingdom

Recruiting
Site contact (verified)
Ann Sergeant, Site 0284+441383623415

Guy's and St Thomas' NHS Foundation Trust - Guy's Hospital

London SE1 9RT, United Kingdom

Recruiting
Site contact (verified)
Richard Woolf, Site 02724402071887188

How to Get in Touch

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

Sponsor contact

CONTACT

855-907-3286 Clinical.Trials@bms.com

First line of the email MUST contain NCT # and Site #.

Sponsor contact

CONTACT

Data sourced from ClinicalTrials.gov · Last verified: 2026-09