Analysis of the antibody level against interferon beta before and after increase of dose in MS therapy

CompletedPhase 4MS (type not specified)2005-001008-37

What it found

No results found

We found no results in the registry or in papers.

What was tested

Treatment tested

What it measured

Main measures

  • Evaluation of the level of binding and neutralizing antibodies to interferin beta before and after increase of the dose from 22 to 44 micrograms/dose, with two years of follow-up after the change of dose

    Immune response

Who could take part

MS (type not specified)

Show the full criteria

Inclusion criteria

Inclusion: Multiple sclerosis patients aged 18-65 years treated by Rebif 22 microgram/dose for more than 1 year. Exclusion: Insufficient patient compliance.

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

To determine whether increase from 22 microgram to 44 microgram per dose interferon beta-1a three times a week will reduce the level of binding and neutralizing antibodies to interferon beta by high dose tolerance or other mechanisms.

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History

    1. Started

      Mar 2005

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