Natalizumab
DrugNatalizumab 300 mg IV infusion, every 4 weeks, for up to 116 weeks.
Other names: Tysabri
NCT Number: NCT00027300
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.
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Notify Me18 year–50 year
All sexes
Interventional
Phase 3
Algemeen Ziekenhuis St. Jan, Bruges, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Natalizumab 300 mg IV infusion, every 4 weeks, for up to 116 weeks.
Other names: Tysabri
Placebo, IV infusion, every 4 weeks, for up to 116 weeks.
Time frame: 1 year and 2 years
Time frame: 1 year
Biogen
Industry
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Determine the Safety and Efficacy of Natalizumab in Subjects With Relapsing-Remitting Multiple Sclerosis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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