Actively Recruiting

Age: 50Years +
All Genders
ID07313462

Escalation vs. Induction Therapy Strategy in Patients With Early-Onset Multiple Sclerosis After Age 50

Led by University Hospital, Strasbourg, France · Updated on 2026-01-02

830

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational study focuses on patients diagnosed with relapsing-remitting multiple sclerosis (RRMS) who had their first symptoms after age 50. Researchers aim to evaluate the risk of inflammatory disease activity by comparing two therapeutic approaches: escalation therapy and induction therapy. The study also seeks to identify factors linked to inflammation relapse and complications related to treatment. The trial is sponsored by the University Hospital in Strasbourg, France. The study compares two treatment strategies involving disease-modifying antirheumatic drugs (DMARDs). One group receives moderately effective DMARDs such as teriflunomide, dimethyl fumarate or diroximel fumarate, glatiramer acetate, interferon beta, or peginterferon. The other group receives highly effective DMARDs, including fingolimod, ponesimod, natalizumab, rituximab, ocrelizumab, ofatumumab, or cladribine. Participants started their first therapy within two years of symptom onset. Participants will be observed for up to 12 months to measure the time until the first clinical inflammatory relapse. Researchers will review medical histories and analyze treatment-related outcomes. The study does not involve administering treatments but collects data retrospectively. This approach helps to understand disease activity and treatment effects in patients with late-onset MS.

CONDITIONS

Brief Title

Escalation vs. Induction Therapy Strategy in Patients With Early-Onset MS After Age 50

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with relapsing-remitting multiple sclerosis (RRMS) onset after age 50
  • Patients who started their first disease-modifying therapy within 2 years of the first symptoms
  • Patients treated with moderately effective disease-modifying antirheumatic drugs (teriflunomide, dimethyl fumarate, diroximel fumarate, glatiramer acetate, interferon beta, peginterferon)
  • Patients treated with highly effective disease-modifying antirheumatic drugs (fingolimod, ponesimod, natalizumab, rituximab, ocrelizumab, ofatumumab, cladribine)
Not Eligible

You will not qualify if you...

  • Patients with early progressive multiple sclerosis

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 12 months

Participants are observed to monitor disease progression and treatment effects over time.

Trial Site Locations

Total: 1 location

1

Centre d'Investigation Clinique - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

N

Nicolas Collongues, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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