Compares two psoriasis drugs, deucravacitinib and ustekinumab, for long-term safety
Tests deucravacitinib against ustekinumab over time in adults with plaque psoriasis.
Plain-language title generated from the registry record
Registry title: Long-Term Safety Study of Deucravacitinib Versus Ustekinumab in Participants With Psoriasis (PRAGMATYK)
Key facts
- Where
- Ajax, Barrie, Calgary, Edmonton, Hamilton, Kelowna, London, Markham, Mississauga, Montreal, Nanaimo, Newmarket, North Bay, Oakville, Ottawa, Peterborough, Québec, Richmond Hill, Sherbrooke, St. John's, Surrey, Toronto, Verdun, and Winnipeg, CanadaSee the 34 sites
- Phase
- Phase 3
Where in Canada
- CCA Medical ResearchAjax, CanadaTaking people
- SimcoDerm Medical and Surgical Dermatology CenterBarrie, CanadaTaking people
- Beacon DermatologyCalgary, CanadaTaking people
- Dermatology Research InstituteCalgary, CanadaTaking people
- CalgaryCalgary, CanadaNo longer taking part
- Alberta Dermasurgery CentreEdmonton, CanadaTaking people
- Laser Rejuvenation Clinics Edmonton D.T. Inc.Edmonton, CanadaTaking people
- Stratica DermatologyEdmonton, CanadaTaking people
- Vida Clinic ResearchEdmonton, CanadaTaking people
- HamiltonHamilton, CanadaNot yet recruiting
- Interior Dermatology CentreKelowna, CanadaTaking people
- Centricity Research London Victoria MultispecialtyLondon, CanadaTaking people
- DermeffectsLondon, CanadaTaking people
- Lovegrove DermatologyLondon, CanadaTaking people
- Lynderm Research Inc.Markham, CanadaTaking people
- DermEdgeMississauga, CanadaTaking people
- Centre de Recherche Saint-LouisMontreal, CanadaTaking people
- Skin Care WestNanaimo, CanadaTaking people
- Ryan Clinical Research IncNewmarket, CanadaTaking people
- North Bay Dermatology CentreNorth Bay, CanadaTaking people
- The Centre for Clinical Trials Inc.Oakville, CanadaTaking people
- JRB Research Inc.Ottawa, CanadaTaking people
- SKiN Centre for DermatologyPeterborough, CanadaTaking people
- Centre de Recherche Saint-LouisQuébec, CanadaTaking people
- The Centre for DermatologyRichmond Hill, CanadaTaking people
- Centre de Recherche Saint-LouisSherbrooke, CanadaTaking people
- Dr Tracey Brown-Maher Dermatology Clinic and Research CentreSt. John's, CanadaTaking people
- SurreySurrey, CanadaNot yet recruiting
- Enverus Medical ResearchSurrey, CanadaTaking people
- Avenue Research GroupToronto, CanadaTaking people
- North York Research Inc.Toronto, CanadaTaking people
- Toronto Research CentreToronto, CanadaTaking people
- Sima RechercheVerdun, CanadaTaking people
- Wiseman Dermatology Research Inc.Winnipeg, CanadaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Bristol-Myers Squibb
- Trial code
- NCT07116967EU 2023-503766-24-00
- Record updated
- 28 October 2026
- Original description
A study to evaluate the long-term safety of Deucravacitinib versus Ustekinumab in participants with psoriasisRead full original descriptionShow less
A Phase 3b/4 Multi-center, Randomized, Open-label, Long-term Safety Study of Deucravacitinib in Comparison to Ustekinumab in Participants With Moderate-to-Severe Plaque Psoriasis
A study to evaluate the long-term safety of Deucravacitinib versus Ustekinumab in participants with psoriasis
Inclusion: Participants with moderate-to-severe plaque psoriasis:; Deemed by the Investigator to be a candidate for phototherapy or systemic treatment for psoriasis, including ustekinumab; 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: 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.