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  • NCT07256015

Recruiting

Deucravacitinib for Patients With Moderate/Severe Psoriasis: A Real-Life Experience in Italy - IM011-1228

Updated: 27 November, 2025   |   ClinicalTrials.gov

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CONSIDERING THIS TRIAL?
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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.
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Trial Details

  • Gender(s)

  • 18+

    Age Range

  • 1

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Cohort 1

Key Eligibility Criteria

Inclusion Criteria: - Participants have initiated treatment with deucravacitinib monotherapy 4 to 8 weeks earlier according to clinical practice and to reimbursement criteria determined by National Drug Agency in Italy (AIFA) - Patients have moderate to severe plaque psoriasis - Patients have signed informed consent form (ICF) Exclusion Criteria: - Simultaneous participation in any interventional study for their moderate-to-severe psoriasis - Inability to participate to the study for the following reasons: patients unable to understand the aim of the study, patients unable to understand and sign the ICF

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We recommend that you also contact BMS to report side effects.
Side effects and other reportable events are defined here
Report side effects or product quality complaints: Medical Information

466-DK-2200001