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Clinical Trial Summary

Primary Objective: To determine the dose-response relationship for SAR442168 to reduce the number of new active brain lesions. Secondary Objectives: - To evaluate efficacy of SAR442168 on disease activity as assessed by imaging measures. - To evaluate the safety and tolerability of SAR442168.


Clinical Trial Description

The total study duration was 24 weeks which included a screening period of 4 weeks, a treatment period of 16 weeks, and a follow-up period of up to 4 weeks. Participants who completed the Week 16 visit were proposed to be enrolled in a long-term extension safety and efficacy study to assess safety, tolerability and efficacy of SAR442168. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03889639
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 2
Start date March 29, 2019
Completion date January 2, 2020

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