Last updated on September 2020

Long Term Safety and Efficacy Study of SAR442168 in Participants With Relapsing Multiple Sclerosis


Brief description of study

Primary Objective:

To determine the long-term safety and tolerability of SAR442168 in RMS participants

Secondary Objective:

To evaluate efficacy of SAR442168 on disease activity, assessed by clinical and imaging methods

Detailed Study Description

Approximately 62 months including the 8 weeks post-treatment visit

Clinical Study Identifier: NCT03996291

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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