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Cerca in Study Connect
  • NCT05701995

Recruiting

A Study to Evaluate the Effect of Deucravacitinib on Quality of Life in Participants With Plaque Psoriasis in a Community Setting - IM011-237

Aggiornato: 26 febbraio, 2024   |   ClinicalTrials.gov

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SELEZIONI UNA LINGUA

Dettagli della sperimentazione

  • Phase 4

    Fase

  • Sesso

  • 18+

    Fascia d'età

  • 36

    Sede/i

  • Recruiting

Opzioni di trattamento

Bracci dello studio
TERAPIA ASSEGNATA
Experimental: Deucravacitinib
Drug: Deucravacitinib
Placebo Comparator: Placebo then Deucravacitinib
Drug: Deucravacitinib Other: Placebo

Principali criteri di idoneità

Inclusion Criteria - Men and women diagnosed with stable plaque psoriasis for 6 months or more. Stable psoriasis is defined as no morphology changes or significant flares of disease activity in the opinion of the investigator. - Deemed by the investigator to be a candidate for phototherapy or systemic therapy. - ≥ 3% of Body Surface Area (BSA) involvement at Screening Visit and Day 1 - Dermatology Life Quality Index (DLQI) score > 5 at Screening Visit and Day 1 Exclusion Criteria: Target Disease Exceptions: - Non-plaque psoriasis (that is, guttate, pustular, erythrodermic, palmoplantar only involvement or drug-induced psoriasis) at Screening Visit or Day 1 Other protocol-defined inclusion/exclusion criteria apply.

Ti consigliamo vivamente di contattare BMS per segnalare gli effetti collaterali (eventi avversi)
Qui vengono definiti gli effetti collaterali (eventi avversi) e altri eventi da segnalare
Segnala effetti collaterali (eventi avversi) o reclami sulla qualità del prodotto: informazioni mediche

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