MSFrontier

ENSURE-2

A Multi-Center, Randomized, Double-Blinded Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of IMU-838 versus Placebo in Adults with Relapsing Multiple Sclerosis (ENSURE-2)
Moved to EU CTIS registryPhase 3Relapsing MS2021-000029-28

What was tested

Treatment tested

  • Vidofludimus

    Dihydroorotate dehydrogenase inhibitor

What it measured

Main measures

  • Time to first confirmed relapse, as determined by the Independent Neurology Evaluation Committee (INEC), relapse occurred after the start of treatment administration and before the end of the main period (EOMP), censored at a maximum of 72 weeks, Visit 8 (V8)/EOMP.

    Relapses

Other measures (1)

  • Key secondary efficacy:

Papers

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    History

    1. In scope changed from true to false

    1. Started

      May 2022

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