IM047-050
What it found
No result yet.
What was tested
Treatment tested
- Ozanimod
Sphingosine 1-phosphate receptor 5 modulator
Compared with
Placebo or sham
- Placebo
- Ozanimod HCl 0.23 mg , Ozanimod HCl 1 mg , Ozanimod HCl 0.0575 mg , Ozanimod HCl 0.25 mg
- Fingolimod 0.25 mg capsule, Fingolimod 0.5 mg capsule
What it measured
Main measures
Annualized relapse rate (ARR)
Up to 2 years
RelapsesCore phase: To assess rate of Multiple Sclerosis (MS) relapse over 2 years
Relapses
Other measures (13)
Proportion of participants who did not have a confirmed relapse
At 12 and 24 months
RelapsesNumber of gadolinium enhancing (GdE) T1 lesions
At month 6 and month 12
MRI lesionsNumber of new or newly enlarging hyperintense lesions on T2 magnetic resonance imaging (MRI) sequences
At 6, 12, 18, and 24 months
MRI lesionsIncidence of treatment-emergent adverse events (TEAEs) over the treatment period and over the post-treatment follow-up period
Up to 87 months
SafetyIncidence of adverse event of special interests (AESIs) over the treatment period and over the post-treatment follow-up period
Up to 87 months
SafetyAdverse events (AEs) leading to discontinuation over the treatment period and over the post-treatment follow-up period
Up to 87 months
SafetySteady state plasma concentrations of ozanimod
At day 90
How the body handles the medicineSteady state plasma concentrations of the primary active metabolite CC112273
At day 90
How the body handles the medicineChange from baseline pharmacodynamics (PD) biomarkers of absolute lymphocyte count
At day 90 and throughout the study up to 24 months
Blood or spinal fluid markersImmune responseCore and Extension Phase: proportion of the participants who have worsening or improving RRMS
Who could take part
Relapsing MS · 10 to 17
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.
As registered. Criteria can change, so ask the trial team or your neurologist.
Contact details on the registryAbout this trial
In the sponsor's words
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).
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History
Started
Apr 2025
Main results due
Apr 2031
Finished
Jul 2036
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