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The primary objective of this study is to better understand the pathophysiological background of end-of-dose symptoms (EOD) and thereby determine the percentage of participants who develop EOD under n...
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Lead Sponsor
Biogen
NCT07189325 · Relapsing-Remitting Multiple Sclerosis (RRMS), Anti-CD20 Therapy
NCT07663266 · Multiple Sclerosis, Spinal Cord Injury
NCT06170970 · Multiple Sclerosis, Multiple Sclerosis Fatigue
NCT06782490 · Multiple Sclerosis Spasticity
NCT07299019 · Secondary Progressive Multiple Sclerosis
Klinik für Neurologie, Universitätsklinikum Düsseldorf
Düsseldorf
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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