Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis

Keith C HayesDepartment of Physical Medicine and Rehabilitation, The University of Western Ontario, London, ON, CanadaAbstract: Dalfampridine extended release (ER) 10 mg is an oral tablet form of the potassium (K+) channel-blocking compounded dalfampridine, also known as fampridine, and chemically&a...

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Autor principal: Hayes KC
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Publicado: Dove Medical Press 2011
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spelling oai:doaj.org-article:ca611cb145b34bab91b18fb7e442dcf52021-12-02T03:46:25ZImpact of extended-release dalfampridine on walking ability in patients with multiple sclerosis1176-63281178-2021https://doaj.org/article/ca611cb145b34bab91b18fb7e442dcf52011-04-01T00:00:00Zhttp://www.dovepress.com/impact-of-extended-release-dalfampridine-on-walking-ability-in-patient-a7273https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Keith C HayesDepartment of Physical Medicine and Rehabilitation, The University of Western Ontario, London, ON, CanadaAbstract: Dalfampridine extended release (ER) 10 mg is an oral tablet form of the potassium (K+) channel-blocking compounded dalfampridine, also known as fampridine, and chemically 4-aminopyridine or 4-AP, which received regulatory approval in the United States for the treatment of walking in patients with multiple sclerosis (MS) in January 2010. Two pivotal Phase 3 clinical trials demonstrated significant improvements in walking in patients with the four primary forms of MS following administration of dalfampridine ER tablets 10 mg twice daily. The drug is thought to act by restoring conduction in focally demyelinated axons and by enhancing neurotransmission, thereby leading to improved neurological function. This review describes how dalfampridine represents a new pharmacotherapeutic approach to the clinical management of mobility impairment. It describes the mechanism of action and chemistry of dalfampridine ER, its pharmacokinetics, tolerability, and side effects, and the outcomes of multicenter trials showing its efficacy in improving walking speed. Clinician and patient global assessments, as well as patient self-assessment of the impact of MS on their gait disability, confirm clinically relevant benefit from the therapy. Patients tolerate the drug well and their improvement in terms of household and community ambulation, inferred from analysis of pooled data from several studies, is likely to translate into benefits in the performance of instrumental activities of daily living and a reduction in the neuropsychiatric burden of disease.Keywords: dalfampridine ER, Ampyra®, fampridine-SR, 4-aminopyridine, multiple sclerosis, demyelinationHayes KCDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2011, Iss Issue 1, Pp 229-239 (2011)
institution DOAJ
collection DOAJ
language EN
topic Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Hayes KC
Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
description Keith C HayesDepartment of Physical Medicine and Rehabilitation, The University of Western Ontario, London, ON, CanadaAbstract: Dalfampridine extended release (ER) 10 mg is an oral tablet form of the potassium (K+) channel-blocking compounded dalfampridine, also known as fampridine, and chemically 4-aminopyridine or 4-AP, which received regulatory approval in the United States for the treatment of walking in patients with multiple sclerosis (MS) in January 2010. Two pivotal Phase 3 clinical trials demonstrated significant improvements in walking in patients with the four primary forms of MS following administration of dalfampridine ER tablets 10 mg twice daily. The drug is thought to act by restoring conduction in focally demyelinated axons and by enhancing neurotransmission, thereby leading to improved neurological function. This review describes how dalfampridine represents a new pharmacotherapeutic approach to the clinical management of mobility impairment. It describes the mechanism of action and chemistry of dalfampridine ER, its pharmacokinetics, tolerability, and side effects, and the outcomes of multicenter trials showing its efficacy in improving walking speed. Clinician and patient global assessments, as well as patient self-assessment of the impact of MS on their gait disability, confirm clinically relevant benefit from the therapy. Patients tolerate the drug well and their improvement in terms of household and community ambulation, inferred from analysis of pooled data from several studies, is likely to translate into benefits in the performance of instrumental activities of daily living and a reduction in the neuropsychiatric burden of disease.Keywords: dalfampridine ER, Ampyra®, fampridine-SR, 4-aminopyridine, multiple sclerosis, demyelination
format article
author Hayes KC
author_facet Hayes KC
author_sort Hayes KC
title Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
title_short Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
title_full Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
title_fullStr Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
title_full_unstemmed Impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
title_sort impact of extended-release dalfampridine on walking ability in patients with multiple sclerosis
publisher Dove Medical Press
publishDate 2011
url https://doaj.org/article/ca611cb145b34bab91b18fb7e442dcf5
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