A prospective pilotstudy of immunological and radiological effects of intrathecal rituximab in patients with secondary progressive multiple sclerosis

Stopped earlyPhase 2Progressive MS2012-004436-36

What it found

Stopped

The trial ended early for another reason (see below).

What was tested

Treatment tested

  • Rituximab

    B-lymphocyte antigen CD20 binding agent

What it measured

Main measures

  • Change in spinal fluid immune respons after 1 and 3 month

Other measures (1)

  • Safety (Adverse events)

    Safety

Who could take part

Progressive MS

Show the full criteria

Inclusion criteria

Inclusion: Clinical definate multiple sclerosis Exclusion: Pregnancy and lactation

Exclusion criteria

Not separately supplied in the registry.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The aim of this study is to investigate the safety of intrathecal administered Rituximab to patients with secondary progressive multiple sclerosis, based upon analysis of the intrathecal and periferal immune response.

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History

    1. Started

      Apr 2013

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