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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

About this study

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

Based on ClinicalTrials.gov records.

PhasePhase 3
DrugFrexalimab

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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