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A Study for Tysabri Participant Preference

Relapsing-Remitting Multiple Sclerosis (RRMS) Clinical Trial

Official title:
SISTER - Subcutaneous: Non-Interventional Study for Tysabri Patient Preference - Experience From Real World

Clinical Trial Summary

The primary objective of this study is to collect, evaluate and compare data on participant preference between subcutaneous (SC) and intravenous (IV) natalizumab. The secondary objectives of this study are to evaluate the immunogenicity of SC natalizumab for natalizumab-naïve participants and collect and evaluate data on the multiple sclerosis (MS) disease-relevant parameters (relapse rate, time to first relapse, disability improvement and progression) over 12 months, in participants with natalizumab therapy starting on SC natalizumab or switching from IV natalizumab.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Multiple Sclerosis
  • Multiple Sclerosis, Relapsing-Remitting
  • Relapsing-Remitting Multiple Sclerosis (RRMS)
Clinical Trial Details
NCT number NCT05304520
Study type Observational
Source Biogen
Contact
Status Completed
Phase
Start date October 12, 2021
Completion date April 30, 2024
View Details
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