RecruitingPhase 3Relapsing MSNCT064082592022-501332-42-00

What it found

Still running

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

    Relapses
  • Core 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

    Relapses
  • Number of gadolinium enhancing (GdE) T1 lesions

    At month 6 and month 12

    MRI lesions
  • Number of new or newly enlarging hyperintense lesions on T2 magnetic resonance imaging (MRI) sequences

    At 6, 12, 18, and 24 months

    MRI lesions
  • Incidence of treatment-emergent adverse events (TEAEs) over the treatment period and over the post-treatment follow-up period

    Up to 87 months

    Safety
  • Incidence of adverse event of special interests (AESIs) over the treatment period and over the post-treatment follow-up period

    Up to 87 months

    Safety
  • Adverse events (AEs) leading to discontinuation over the treatment period and over the post-treatment follow-up period

    Up to 87 months

    Safety
  • Steady state plasma concentrations of ozanimod

    At day 90

    How the body handles the medicine
  • Steady state plasma concentrations of the primary active metabolite CC112273

    At day 90

    How the body handles the medicine
  • Change 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 response
  • Core 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 registry

About 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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Related trials

History

    1. Started

      Apr 2025

    2. Main results due

      Apr 2031

    3. Finished

      Jul 2036

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