Dose-finding Study for SAR442168 in Relapsing Multiple Sclerosis

Status Completed

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

Clinical Trial Details

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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