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A Post-Authorization, Long-term Study of Ozanimod Real-world Safety — ORION  

Multiple Sclerosis, Relapsing-Remitting Clinical Trial

Official title:
ORION (Ozanimod Real-World Safety - A Post- Authorisation Multi-National Long-term Non-Interventional Study)

Clinical Trial Summary

The purpose of this study is to determine the rates of adverse events of interest (AEIs) in a real-world population of participants with relapsing remitting multiple sclerosis (RRMS) receiving Ozanimod, sphingosine-1 phosphate (S1P) receptor modulator, compared to the rates of these events in two population of participants: - Participants not exposed to ozanimod with RRMS who have received treatment with other S1P-receptor modulators disease modifying treatments (DMTs) - Participants not exposed to ozanimod with RRMS who have received treatment with other non-S1P-receptor modulators disease modifying treatments (DMTs)

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05605782
Study type Observational
Source Bristol-Myers Squibb
Contact
Status Active, not recruiting
Phase
Start date June 30, 2022
Completion date December 31, 2032
View Details
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