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  • NCT07256015

Recruiting

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

Opdateret: 27 november, 2025   |   ClinicalTrials.gov

Udskriftsvenligt sammendrag

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VÆLG SPROG

Forsøgsdetaljer

  • Køn

  • 18+

    Aldersinterval

  • 1

    Beliggenhed(er)

  • Recruiting

Behandlingsmuligheder

Forsøgsgrene
TILDELT INTERVENTION
Cohort 1
Drug: Deucravacitinib

Primære egnethedskriterier

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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