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Szukaj Study Connect
  • NCT07256015

Recruiting

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

Zaktualizowano: 27 listopad, 2025   |   ClinicalTrials.gov

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Szczegóły badania

  • Płeć

  • 18+

    Zakres wieku

  • 1

    Lokalizacje

  • Recruiting

Opcje leczenia

Grupy badania
PRZYPISANA INTERWENCJA
Cohort 1
Drug: Deucravacitinib

Kluczowe kryteria kwalifikacyjne

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