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RECRUITING Phase 3

Study to Evaluate the Effectiveness and Safety of Ozanimod Compared to Fingolimod in Children and Adolescents With Relapsing Remitting Multiple Sclerosis

NCT06408259 · View on ClinicalTrials.gov ↗

Study Summary

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).

Interventions

  • OTHER Placebo
  • DRUG Ozanimod
  • DRUG Fingolimod

Study Locations (20)

California

  • Local Institution - 0114 — Loma Linda
  • University of California Davis Health — Sacramento

Illinois

  • Local Institution - 0093 — Chicago
  • University of Chicago Medical Center — Chicago

New Jersey

  • Local Institution - 0131 — New Brunswick
  • Local Institution - 0132 — Teaneck

Lombardy

  • Ospedale San Raffaele — Milan
  • Local Institution - 0081 — Milan

Florida

  • University of South Florida — Tampa

Kentucky

  • Local Institution - 0047 — Louisville

Ohio

  • Local Institution - 0091 — Cincinnati

Oregon

  • Local Institution - 0092 — Portland

Trial Details

FieldValue
Enrollment Target 194 participants
Start Date 2025-04-08
Est. Completion 2036-07-13
Phase Phase 3

Sponsor

Celgene

73 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06408259

The ClinicalTrials.gov registry entry for NCT06408259 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 194 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Celgene, which has 73 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Multiple Sclerosis, Relapsing-Remitting appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06408259 reports 20 study locations spanning 16 distinct geographic areas — top geographies include California, Illinois, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06408259 about?

NCT06408259 is a clinical study titled "Study to Evaluate the Effectiveness and Safety of Ozanimod Compared to Fingolimod in Children and Adolescents With Relapsing Remitting Multiple Sclerosis". 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).

What is the current status of trial NCT06408259?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 194 participants. The study started on 2025-04-08. Estimated completion is 2036-07-13.

What conditions does trial NCT06408259 study?

This clinical trial studies the following conditions: Multiple Sclerosis, Relapsing-Remitting. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06408259?

The interventions under investigation include: Placebo (OTHER), Ozanimod (DRUG), Fingolimod (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06408259?

This trial is sponsored by Celgene, which has 73 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06408259 being conducted?

This trial has 20 study locations across California, Florida, Illinois, Kentucky, New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial