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Update on once-daily zonisamide monotherapy in partial seizures

Zonisamide is an antiepileptic drug that is structurally different from other antiepileptic agents. Its long half-life, once-daily dosing, lack of induction of hepatic enzymes, and broad spectrum of action makes it a suitable candidate for monotherapy. It has been approved as monotherapy for partial...

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Autores principales: Afra, Pegah, Adamolekun, Bola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964158/
https://www.ncbi.nlm.nih.gov/pubmed/24672240
http://dx.doi.org/10.2147/NDT.S39152
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author Afra, Pegah
Adamolekun, Bola
author_facet Afra, Pegah
Adamolekun, Bola
author_sort Afra, Pegah
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description Zonisamide is an antiepileptic drug that is structurally different from other antiepileptic agents. Its long half-life, once-daily dosing, lack of induction of hepatic enzymes, and broad spectrum of action makes it a suitable candidate for monotherapy. It has been approved as monotherapy for partial onset epilepsy in Japan and South Korea for more than a decade, and was recently approved as monotherapy in Europe. In the USA, it is only approved by the US Food and Drug Administration for adjunctive treatment of partial onset epilepsy. In this paper, we briefly review the literature on zonisamide monotherapy in partial onset epilepsy with regard to its efficacy, safety, tolerability, and long-term side effects, including a recent noninferiority trial in comparison with extended-release carbamazepine. While European regulatory agencies use noninferiority trials for approval of monotherapy, such a trial design does not meet the current regulatory requirements for approval as monotherapy in the USA.
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spelling pubmed-39641582014-03-26 Update on once-daily zonisamide monotherapy in partial seizures Afra, Pegah Adamolekun, Bola Neuropsychiatr Dis Treat Review Zonisamide is an antiepileptic drug that is structurally different from other antiepileptic agents. Its long half-life, once-daily dosing, lack of induction of hepatic enzymes, and broad spectrum of action makes it a suitable candidate for monotherapy. It has been approved as monotherapy for partial onset epilepsy in Japan and South Korea for more than a decade, and was recently approved as monotherapy in Europe. In the USA, it is only approved by the US Food and Drug Administration for adjunctive treatment of partial onset epilepsy. In this paper, we briefly review the literature on zonisamide monotherapy in partial onset epilepsy with regard to its efficacy, safety, tolerability, and long-term side effects, including a recent noninferiority trial in comparison with extended-release carbamazepine. While European regulatory agencies use noninferiority trials for approval of monotherapy, such a trial design does not meet the current regulatory requirements for approval as monotherapy in the USA. Dove Medical Press 2014-03-19 /pmc/articles/PMC3964158/ /pubmed/24672240 http://dx.doi.org/10.2147/NDT.S39152 Text en © 2014 Afra and Adamolekun. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Afra, Pegah
Adamolekun, Bola
Update on once-daily zonisamide monotherapy in partial seizures
title Update on once-daily zonisamide monotherapy in partial seizures
title_full Update on once-daily zonisamide monotherapy in partial seizures
title_fullStr Update on once-daily zonisamide monotherapy in partial seizures
title_full_unstemmed Update on once-daily zonisamide monotherapy in partial seizures
title_short Update on once-daily zonisamide monotherapy in partial seizures
title_sort update on once-daily zonisamide monotherapy in partial seizures
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964158/
https://www.ncbi.nlm.nih.gov/pubmed/24672240
http://dx.doi.org/10.2147/NDT.S39152
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