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Rechercher 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

Mis à jour: 26 février, 2024   |   ClinicalTrials.gov

Résumé imprimable

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SÉLECTIONNER LA LANGUE

Détails de l’essai

  • Phase 4

    Phase

  • Sexe(s)

  • 18+

    Tranche d’âge

  • 36

    Site(s)

  • Recruiting

Options de traitement

Bras de l’étude
INTERVENTION ASSIGNÉE
Experimental: Deucravacitinib
Drug: Deucravacitinib
Placebo Comparator: Placebo then Deucravacitinib
Other: Placebo Drug: Deucravacitinib

Principaux critères d’éligibilité

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.

Nous vous recommandons vivement de contacter BMS pour signaler les effets secondaires (événements indésirables)
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici
Signaler des plaintes concernant des effets indésirables (effets indésirables) ou des produits: Informations médicales