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Clinical Trial Summary

National, multicenter study: The study consists of 3 periods: 1. A baseline visit to confirm that patient is still in CIS status. All patients will be clinically evaluated for CDMS and an MRI (less than 2 months) will be analyzed to exclude MS patients according to 2010 Mc Donald's criteria. 2. Treatment period with timed evaluations 3. Post-treatment period: 4 weeks, with 2 visits following study drug discontinuation and accelerated elimination procedure. All patients who discontinue the study drug and according to investgator's decision, will perform the accelerated elimination procedure and the post- accelerated elimination visits (at 2 and 4 weeks after the end of treatment (EOT).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02587195
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact
Status Completed
Phase Phase 3
Start date December 18, 2015
Completion date August 31, 2021

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