Clinical Trials in France / NCT07313462
Recruiting
Observational
Escalation vs. Induction Therapy Strategy in Patients With Early-Onset MS After Age 50
NCT07313462 · tracked via the Priya Life Science France tracker
Condition(s) studied
Multiple Sclerosis (MS)
Study summary
The objective of this study is to evaluate the risk of inflammatory disease activity by retrospectively comparing two therapeutic strategies (escalation group and induction group). The investigators also aim to identify factors associated with inflammatory relapse and treatment-related complications.
Eligibility
Inclusion Criteria:
* Patients with 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 (DMARDs) (teriflunomide, dimethyl fumarate or diroximel fumarate, glatiramer acetate, interferon beta, peginterferon)
* Patient treated with highly effective DMARDs (fingolimod, ponesimod, natalizumab, rituximab, ocrelizumab, ofatumumab, cladribine)
Exclusion Criteria:
\- Patients with early progressive MS
Primary outcome measure(s)
- Time to First Clinical Inflammatory Relapse — Up to 12 months
Compare the time to first clinical inflammatory relapse between two groups of patients who developed relapsing-remitting MS (RRMS) after age 50: * Group 1 = therapeutic escalation strategy: starting with a moderately effective treatment (teriflunomide, dimethyl fumarate or diroximel fumarate, glatiramer acetate, interferon beta, peginterferon) * Group 2 = induction strategy: starting with a highly effective treatment (fingolimod, ponesimod, natalizumab, rituximab, ocrelizumab, ofatumumab, cladribine)
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Centre d'Investigation Clinique - CHU de Strasbourg - France | Strasbourg | France | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07313462 on ClinicalTrials.gov ↗ ← All trials in France