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Active, not recruiting Observational

A Study to Describe the Persistence With Ozanimod Treatment in Relapsing-Remitting Multiple Sclerosis (RRMS) Participants

NCT05811416 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2023-06-14
Last updated
2026-05-29

Condition(s) studied

Relapsing-remitting Multiple Sclerosis (RRMS)

Study summary

The purpose of the study is to collect clinical data on the persistence with ozanimod treatment, as well as to describe its effects on participant-relevant outcome parameters in treatment-naïve participants with RRMS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Relapsing-remitting multiple sclerosis (RRMS) diagnosis by 2017 revised McDonald criteria at the treatment start * Participant who started treatment with ozanimod for the first time 3 months (+/- 2 weeks) before inclusion, according to European Union (EU) Summary of Product Characteristics (SmPC) and/or Spanish therapeutic positioning report (TPR) recommendation and following routine clinical practice of the participating hospital * Low-to-moderate activity, defined as less than 2 relapses in the previous year before starting the treatment with ozanimod Exclusion Criteria: * Prior exposure to ozanimod or any other disease modifier treatment (DMT) for RRMS before starting treatment with ozanimod subject of this study * Participant who has started ozanimod within a clinical trial Note: Other protocol-defined inclusion/exclusion criteria apply

Primary outcome measure(s)

  • Time from ozanimod treatment initiation to ozanimod treatment permanent discontinuation — Up to 24 months
  • Percentage of participants on treatment with ozanimod at 24 months — At month 24

Trial sites (1)

FacilityCityRegionStatus
Local Institution - 0001 Barcelona Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05811416 on ClinicalTrials.gov ↗ ← All trials in Spain