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Antiseizure medication discovery: Recent and future paradigm shifts

Despite the ever‐increasing number of available options for the treatment of epilepsies and the remarkable advances on the understanding of their pathophysiology, the proportion of refractory patients has remained approximately unmodified during the last 100 years. How efficient are we translating p...

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Detalles Bibliográficos
Autor principal: Talevi, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340309/
https://www.ncbi.nlm.nih.gov/pubmed/35090197
http://dx.doi.org/10.1002/epi4.12581
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author Talevi, Alan
author_facet Talevi, Alan
author_sort Talevi, Alan
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description Despite the ever‐increasing number of available options for the treatment of epilepsies and the remarkable advances on the understanding of their pathophysiology, the proportion of refractory patients has remained approximately unmodified during the last 100 years. How efficient are we translating positive outcomes from basic research to clinical trials and/or the clinical scenario? It is possible that fresh thinking and exploration of new paradigms are required to arrive at truly novel therapeutic solutions, as seemingly proven by recently approved first‐in‐class antiseizure medications and drug candidates undergoing late clinical trials. Here, the author discusses some approximations in line with the network pharmacology philosophy, which may result in highly innovative (and, hopefully, safer and/or more efficacious) medications for the control of seizures, as embodied with some recent examples in the field, namely tailored multi‐target agents and low‐affinity ligands.
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spelling pubmed-93403092022-08-02 Antiseizure medication discovery: Recent and future paradigm shifts Talevi, Alan Epilepsia Open Critical Reviews Despite the ever‐increasing number of available options for the treatment of epilepsies and the remarkable advances on the understanding of their pathophysiology, the proportion of refractory patients has remained approximately unmodified during the last 100 years. How efficient are we translating positive outcomes from basic research to clinical trials and/or the clinical scenario? It is possible that fresh thinking and exploration of new paradigms are required to arrive at truly novel therapeutic solutions, as seemingly proven by recently approved first‐in‐class antiseizure medications and drug candidates undergoing late clinical trials. Here, the author discusses some approximations in line with the network pharmacology philosophy, which may result in highly innovative (and, hopefully, safer and/or more efficacious) medications for the control of seizures, as embodied with some recent examples in the field, namely tailored multi‐target agents and low‐affinity ligands. John Wiley and Sons Inc. 2022-02-07 /pmc/articles/PMC9340309/ /pubmed/35090197 http://dx.doi.org/10.1002/epi4.12581 Text en © 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Critical Reviews
Talevi, Alan
Antiseizure medication discovery: Recent and future paradigm shifts
title Antiseizure medication discovery: Recent and future paradigm shifts
title_full Antiseizure medication discovery: Recent and future paradigm shifts
title_fullStr Antiseizure medication discovery: Recent and future paradigm shifts
title_full_unstemmed Antiseizure medication discovery: Recent and future paradigm shifts
title_short Antiseizure medication discovery: Recent and future paradigm shifts
title_sort antiseizure medication discovery: recent and future paradigm shifts
topic Critical Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340309/
https://www.ncbi.nlm.nih.gov/pubmed/35090197
http://dx.doi.org/10.1002/epi4.12581
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