A study of the immune response to vaccination in MS patients treated with alemtuzumab

Stopped earlyPhase 4Relapsing MS2009-011523-31

What it found

Stopped

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

What it measured

Main measures

  • The primary outcome measure will be the antibody response to each vaccine measured at 4 weeks (+/- 7 days) post-vaccination.

    Immune response

Who could take part

Relapsing MS

Show the full criteria

Inclusion criteria

Inclusion: • Male or non-pregnant, non-lactating female patients, 18 to 50 years of age (inclusive) Exclusion: • Previously received Haemophilus b or pneumococcal vaccines or have had Haemophilus or pneumococcal disease (these antigens are intended to be novel to the subject’s immune system)

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 the trial is to determine if vaccinations are effective in patients with multiple sclerosis who have been treated with the lympho-depleting humanised monoclonal antibody alemtuzumab. The primary outcome measure will be the antibody response to each vaccine measured at 4 weeks post-vaccination.

Papers

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    History

      1. Started

        Apr 2009

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