A double-blind, placebo-controlled, randomised trial to prove the therapeutic concept and to determine the pharmacokinetic profile of ATL 1102 (VLA-4 antisense oligonucleotide) by subcutaneous injections in patients with multiple sclerosis.

CompletedPhase 2Relapsing MS2006-004736-79

What it found

No results found

We found no results in the registry or in papers.

What was tested

Treatment tested

  • ATL1102

What it measured

Main measures

  • • the cumulative number of new active lesions (either new gadolinium-enhancing, or non-enhancing, new or enlarging on T2) on MRI (to include all lesions from weeks 4, 8, and 12), corrected for the number of enhancing lesions at baseline

    MRI lesions

Who could take part

Relapsing MS

Show the full criteria

Inclusion criteria

Inclusion: • Males and females aged 18 - 55 years Exclusion: • Administration of any investigational drug within the previous 2 months before enrolment (4 months if the previous drug was a new chemical entity)

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 evaluate the efficacy of a selected treatment regimen of ATL 1102 in patients with Relapsing Remitting MS (RRMS) inflammatory lesions using MRI with gadolinium administration compared to placebo.

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History

    1. Started

      Oct 2006

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