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Trial ID RPC-1063-MS-003  |   NCT05335031

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®)

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Summary

  • Male and Female Gender icon
  • 18+
    Age Range
  • BMS Active Not Yet Recruiting Study icon
    Active, Not Recruiting

Overview

The purpose of this study is to collect real-world data and to gain insights about long-term usage of ozanimod (Zeposia ®), its effect on well-defined outcome parameters comprising participant-relevant outcomes, as well as quality of life, effectiveness, and incidence of adverse events.

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Key Eligibility Criteria

Inclusion Criteria

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:
  • Confirmed diagnosis of relapsing-remitting multiple sclerosis (RRMS)
    1. The decision upon treatment with ozanimod must have been made before enrollment and independently of this non-interventional observational study
      1. 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

        Exclusion Criteria Icon
        :
        • Special warnings, precautions and contraindications specified in the current version of the Summary of Product Characteristics (SmPC)
          1. Hypersensitivity to the active substance(s) or to any of the excipients of ozanimod as specified in the prescribing information must not be enrolled
            1. Participation in any other clinical studies Other protocol-defined inclusion/exclusion criteria apply
              Additional Information *

              Treatment Options

              Study Arms

              ASSIGNED INTERVENTION

              Study Arms

              Participants with relapsing-remitting multiple sclerosis (RRMS) treated with Ozanimod

              ASSIGNED INTERVENTION

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