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Rechercher Study Connect

Recruiting

A Study Investigating the Utilization, Effectiveness and Quality of Life in Clinical Practice in Germany for Participants With Relapsing-remitting Multiple Sclerosis Treated With Ozanimod (Zeposia®) - RPC-1063-MS-003

Mis à jour: 12 avril, 2022   |   ClinicalTrials.gov

Résumé imprimable

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Détails de l’essai

  • Sexe(s)

  • 18+

    Tranche d’âge

  • 1

    Site(s)

  • Recruiting

Options de traitement

Bras de l’étude
INTERVENTION ASSIGNÉE
Participants with relapsing-remitting multiple sclerosis (RRMS) treated with Ozanimod

Principaux critères d’éligibilité

Inclusion Criteria: - Confirmed diagnosis of relapsing-remitting multiple sclerosis (RRMS) - The decision upon treatment with ozanimod must have been made before enrollment and independently of this non-interventional observational study - All data on ozanimod treatment are collected prospectively. The retrospective documentation of ozanimod therapy and enrollment of participants that are already on ozanimod therapy is not allowed Exclusion Criteria: - Special warnings, precautions and contraindications specified in the current version of the Summary of Product Characteristics (SmPC) - Hypersensitivity to the active substance(s) or to any of the excipients of ozanimod as specified in the prescribing information must not be enrolled - Participation in any other clinical studies 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