Actively Recruiting
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
Eligibility Criteria
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)
You will not qualify if you...
- Patients with early progressive multiple sclerosis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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