CompletedPhase 3Relapsing MSNCT00027300

What it found

Met its main goal

The main measure showed a statistically significant benefit.

“Natalizumab reduced the risk of sustained progression of disability by 42 percent over two years (hazard ratio, 0.58; 95 percent confidence interval, 0.43 to 0.77; P<0.001).”
Read by software from the paper's abstract

two years

GroupnValue
natalizumab62717 percent cumulative probability of progression
placebo31529 percent cumulative probability of progression

hazard ratio 0.58 (95% CI 0.43–0.77)

p = <0.001

Total participants: 942

Read by software from the paper's abstract

What was tested

Treatment tested

  • Natalizumab

    Integrin alpha-4/beta-1 inhibitor|Integrin alpha-4/beta-7 inhibitor

Placebo or sham

  • Placebo

What it measured

Main measures

  • The primary objectives of this study are to determine whether natalizumab, when compared with placebo, is effective in reducing the rate of clinical relapses at 1 year and, in slowing the progression of disability at 2 years.

    1 year and 2 years

    Relapses

Other measures (1)

  • Reduction in MRI changes and clinical relapses

    1 year

    RelapsesMRI lesions

Who could take part

Relapsing MS · 18 to 50

Inclusion Criteria: * Diagnosis of MS, as defined by McDonald et al., criteria # 1-4 (McDonald et al., 2001) * Between the ages of 18 and 50, inclusive. * Baseline EDSS score between 0.0 and 5.0, inclusive. * Have experienced at least one relapse within the 12 months prior to randomization. * Cranial MRI scan demonstrating lesion(s) consistent with MS. * Have given written informed consent to participate in the study. Exclusion Criteria: * Primary progressive, secondary progressive, or progressive relapsing MS. * MS relapse has occurred,in the opinion of the investigator, within 50 days prior to randomization and/or the subject has not stabilized from a previous relapse. * A clinically significant infectious illness within 30 days prior to randomization. * History of, or abnormal laboratory results indicative of any significant cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, gastrointestinal, dermatologic, psychiatric, renal and/or other major disease, that in the opinion of the investigator, would preclude the administration of a recombinant humanized antibody immunomodulating agent for 116 weeks. * History of severe allergic or anaphylactic reactions or known drug hypersensitivity. * Unable to perform the Timed 25-foot Walk, 9HPT, and PASAT 3. * Abnormal blood tests performed at the Screening Visit.

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

About this trial

In the sponsor's words

The purpose of this study is to determine the safety and efficacy of natalizumab in the treatment of individuals who have been diagnosed with relapsing remitting multiple sclerosis (MS). It is hoped that natalizumab will prevent certain types of white blood cells from moving out of the bloodstream into organs, including the brain, that are being damaged by autoimmune disease (a disease in which the body's own immune system attacks certain organs). These white blood cells are thought to cause inflammation that can result in lesions (small areas of damage) in the brain. These lesions are thought to be the cause of relapses and disability in MS.

Papers

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Linked trials

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Related trials

History

    1. Started

      Nov 2001

    2. Main results due

      Nov 2004

    3. Finished

      Jan 2005

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