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Study details
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Non-inferiority Study of Frexalimab Subcutaneous Administration Compared to Intravenous Administration in Adult Participants With Multiple Sclerosis

Sanofi
NCT IDNCT07325292ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Ages

18–60

Locations

10 sites in AL, AZ, CA +3

What this study is about

This Phase 3 study is testing Frexalimab in people with multiple sclerosis.

Simplified from trial records by PatientMatch.

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

monoclonal antibody

Endpoints

Secondary: Medical device AEs, ADEs, SAEs, SADEs and device deficiencies throughout the study, Number of participants with adverse events, SAEs, AEs leading to permanent study intervention discontinuation, AESIs, and potentially clinically significant abnormality(PCSA) in laboratory tests, and vital signs during the study period, Pharmacokinetic parameters: Cmax(part A), Pharmacokinetic parameters: Tmax(part A)

Body systems

Neurology