Who Can Participate?
Adults aged 40 or above with moderate to severe plaque psoriasis may participate.
Inclusion Criteria
• Psoriasis on 10% or greater body surface area
• One or more of the following should apply
– Current cigarette smoker (vaping does not qualify)
– Diagnosis of hypertension or dyslipidemia
– Use of blood pressure-lowering medications or lipid-lowering medications
– Type 1 or type 2 diabetes
– Have had heart surgery, cardiac arrest, or stroke
– Obesity (body mass index ≥ 30 kg/m2)
– Family history of heart attacks in a relative younger than 55 or a female immediate family member younger than 65
Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating psoriasis (up to 13 visits)
• Will receive either an investigative oral or subcutaneous treatment (study drug)
• Reimbursement for study-related expenses may be provided
How Long Will The Study Last?
• Approximately 5 years
No Doctors Found
Similar Trials
No Similar Trials FoundThe following information is from ClinicalTrials.gov
Last Update Posted: October 10, 2025
NCT07116967
Bristol-Myers Squibb
Brief Summary:
A study to evaluate the long-term safety of Deucravacitinib versus Ustekinumab in participants with psoriasis
Condition or Disease:
Plaque Psoriasis
Intervention/Treatment:
Drug: Deucravacitinib Drug: UstekinumabPhase:
PHASE3
Ages Eligible for Study:
40 Years and older (ADULT,OLDER_ADULT)
Sexes Eligible for Study:
ALL
Terms and Conditions – ClinicalTrials.gov
Purpose of ClinicalTrials.gov Database. The U.S. National Institutes of Health, Department of Health and Human Services, through its National Library of Medicine, has developed ClinicalTrials.gov to provide patients, family members, and members of the public current information about clinical research studies.
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Last Revised July 2024
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Attention: Privacy Officer
139 Union Street East
Waterloo, Ontario, Canada N2J 1C4
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