CompletedPhase 2Progressive MS2016-000283-41

What was tested

Treatment tested

What it measured

Main measures

  • The primary aim of the study is to assess whether 48 weeks of treatment with dimethyl fumarate can decrease neuroaxonal damage in PPMS as assessed by:

Other measures (1)

  • • Clinical endpoints: comparison of change from screening to week 48 in patients treated with dimethyl fumarate and placebo for the following variables:

Loading reviews and guidelines…

Related trials

History

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

    Jun 2016

Assembled by software from public sources and not checked by people. Each record links to its source. Report an error