Multiple Sclerosis Clinical Trial

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.

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

400

Study ID:

NCT06127095

Recruitment Status:

Recruiting

Sponsor:

Biogen

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There is 1 Location for this study

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Biogen
Cambridge Massachusetts, 02142, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

400

Study ID:

NCT06127095

Recruitment Status:

Recruiting

Sponsor:


Biogen

How clear is this clinincal trial information?

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