Study to Evaluate the Effectiveness and Safety of Ozanimod Compared to Fingolimod in Children and Adolescents With Relapsing Remitting Multiple Sclerosis
Sponsored by Bristol-Myers Squibb
About this study
The purpose of this study is to evaluate the effectiveness, safety, tolerability, drug levels and drug effects of ozanimod compared to fingolimod in children and adolescents with relapsing remitting multiple sclerosis (RRMS).
Where this study is enrolling (5)
- Call 916-734-3588
University of California Davis Health
Sacramento, California
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- Call 813-396-9478
University of South Florida
Tampa, Florida
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University of Chicago Medical Center
Chicago, Illinois
- Call 502-629-5606
University of Louisville, Norton Children's Research Institute
Louisville, Kentucky
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- Call 414-955-0619
Medical College of Wisconsin
Milwaukee, Wisconsin
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Who can participate
Inclusion criteria
- ✓Has a diagnosis of multiple sclerosis (MS) as defined by the 2017 revision of the McDonald Criteria with a relapsing remitting course of disease.
- ✓Meets at least 1 of the following criteria for disease activity:
- ✓i) At least 1 MS relapse/attack in the previous year prior to screening.
- ✓ii) At least 2 MS relapses/attacks in the previous 2 years prior to screening.
- ✓iii) Evidence of 1 or more gadolinium-enhancing (GdE) lesions on magnetic resonance imaging (MRI) within 6 months prior to baseline (including screening MRI).
- ✓\- Has an Expanded Disability Status Scale (EDSS) score of 0 to 5.5, both inclusive.
Exclusion criteria
- ✕Diagnosis of progressive forms of MS.
- ✕Active or chronic disease of the immune system other than MS.
- ✕Clinically relevant cardiovascular, hepatic, neurological other major systematic disease.
- ✕Other protocol-defined Inclusion/Exclusion criteria apply.
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Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.