drugset / Trial / NCT02587195

A Study to Evaluate the Safety of Long Term Treatment With Teriflunomide 14 mg Once Daily in Patients With a First Clinical Episode Suggestive of Multiple Sclerosis in a Long-term Extension Period

NCT02587195

Phase 3 Completed 5 enrolled Centre Hospitalier Universitaire de Nice
NaSingle-groupOpen-labelTreatment

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).

Timeline

Start
2015-12-18
Primary completion
2020-08-31
Completion
2021-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Teriflunomide Small molecule 14 mg

Indications