Moved to EU CTIS registryPhase 3Relapsing MS2020-001205-23

What was tested

Treatment tested

  • Rituximab

    B-lymphocyte antigen CD20 binding agent

Compared with

What it measured

Main measures

  • The primary endpoint is to determine the difference in efficacy and safety between rituximab and ocrelizumab according to the following criteria:

    Safety

Other measures (1)

  • •Proportion of patients with 6-months confirmed disability progression (6M-CDP) as measured by the Expanded disability status scale (EDSS) from baseline to month 24. CDP-EDSS defined as an increase of one point in the EDSS score confirmed after 6 months, with an absence of relapse at the time of assessment.

    Disability progressionRelapses

Papers

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Related trials

History

  1. In scope changed from true to false
  1. Started

    Jun 2020

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