Possible clinical outcome measures for clinical trials in patients with multiple sclerosis

Multiple sclerosis (MS) is a chronic inflammatory and neurodegenerative disease with both clinical and pathological heterogeneity. The complexity of the MS population has offered challenges to the measurement of MS disease progression in therapeutic trials. The current standard clinical outcome meas...

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Main Authors: Myla D. Goldman, Robert W. Motl, Richard A. Rudick
Format: Article
Language:English
Published: SAGE Publishing 2010-07-01
Series:Therapeutic Advances in Neurological Disorders
Online Access:https://doi.org/10.1177/1756285610374117
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spelling doaj-1ec4a15989ff4c1b8262dffca303e10b2020-11-25T03:49:57ZengSAGE PublishingTherapeutic Advances in Neurological Disorders1756-28562010-07-01310.1177/1756285610374117Possible clinical outcome measures for clinical trials in patients with multiple sclerosisMyla D. GoldmanRobert W. MotlRichard A. RudickMultiple sclerosis (MS) is a chronic inflammatory and neurodegenerative disease with both clinical and pathological heterogeneity. The complexity of the MS population has offered challenges to the measurement of MS disease progression in therapeutic trials. The current standard clinical outcome measures are relapse rate, Expanded Disability Severity Scale (EDSS), and the MS Functional Composite (MSFC). These measures each have strengths and some weakness. Two additional measures, the six-minute walk and accelerometry, show promise in augmenting current measures. MS therapeutics is a quickly advancing field which requires sensitive clinical outcome measures that can detect small changes in disability that reliably reflect long-term changes in sustained disease progression in a complex population. A single clinical outcome measure of sustained disease progression may remain elusive. Rather, an integration of current and new outcome measures may be most appropriate and utilization of different measures depending on the MS population and stage of the disease may be preferred.https://doi.org/10.1177/1756285610374117
collection DOAJ
language English
format Article
sources DOAJ
author Myla D. Goldman
Robert W. Motl
Richard A. Rudick
spellingShingle Myla D. Goldman
Robert W. Motl
Richard A. Rudick
Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
Therapeutic Advances in Neurological Disorders
author_facet Myla D. Goldman
Robert W. Motl
Richard A. Rudick
author_sort Myla D. Goldman
title Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
title_short Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
title_full Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
title_fullStr Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
title_full_unstemmed Possible clinical outcome measures for clinical trials in patients with multiple sclerosis
title_sort possible clinical outcome measures for clinical trials in patients with multiple sclerosis
publisher SAGE Publishing
series Therapeutic Advances in Neurological Disorders
issn 1756-2856
publishDate 2010-07-01
description Multiple sclerosis (MS) is a chronic inflammatory and neurodegenerative disease with both clinical and pathological heterogeneity. The complexity of the MS population has offered challenges to the measurement of MS disease progression in therapeutic trials. The current standard clinical outcome measures are relapse rate, Expanded Disability Severity Scale (EDSS), and the MS Functional Composite (MSFC). These measures each have strengths and some weakness. Two additional measures, the six-minute walk and accelerometry, show promise in augmenting current measures. MS therapeutics is a quickly advancing field which requires sensitive clinical outcome measures that can detect small changes in disability that reliably reflect long-term changes in sustained disease progression in a complex population. A single clinical outcome measure of sustained disease progression may remain elusive. Rather, an integration of current and new outcome measures may be most appropriate and utilization of different measures depending on the MS population and stage of the disease may be preferred.
url https://doi.org/10.1177/1756285610374117
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