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A Study to Assess New Participant’s Perspectives Beyond Clinical Efficacy of Monoclonal Antibody-Based Relapsing Remitting Multiple Sclerosis (RRMS) Treatments Summary The primary objective of the study is to understand what the added value of natalizumab (Tysabri®) treatment is from a participant's perspective at a given time, based on a one-shot survey. The secondary objectives of the study also aim to characterize the participant's decision-making process to get the treatment; the burden of treatment, characterization of the study population, assessment of the quality of life (QoL), and fatigue dimension.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: • Participants diagnosed with RRMS and followed by a neurologist in France. Exclusion Criteria: • Lack of literacy Note: Other protocol-defined Inclusion/Exclusion criteria may apply.
Check Your Eligibility
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There is 1 Location for this study
Biogen Cambridge Massachusetts, 02142, United States
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