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  • NCT05335031

Active, Not 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

Updated: 21 February, 2025   |   ClinicalTrials.gov

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Trial Details

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Participants with relapsing-remitting multiple sclerosis (RRMS) treated with Ozanimod
Drug: Ozanimod

Key Eligibility Criteria

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

If you want to report a side effect, you can report directly to the Danish Medicines Agency via the website www.meldenbivirkning.dk
We recommend that you also contact BMS to report side effects.
Side effects and other reportable events are defined here
Report side effects or product quality complaints: Medical Information

466-DK-2200001