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Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas

Amyotrophic lateral sclerosis (ALS) is an extremely heterogeneous disease of motor neurons that eventually leads to death. Despite impressive advances in understanding the genetic, molecular, and pathological mechanisms of the disease, the only drug approved to date by both the FDA and EMA is riluzo...

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Detalles Bibliográficos
Autores principales: Khamaysa, Mohammed, Pradat, Pierre-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605458/
https://www.ncbi.nlm.nih.gov/pubmed/36294741
http://dx.doi.org/10.3390/jpm12101601
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author Khamaysa, Mohammed
Pradat, Pierre-François
author_facet Khamaysa, Mohammed
Pradat, Pierre-François
author_sort Khamaysa, Mohammed
collection PubMed
description Amyotrophic lateral sclerosis (ALS) is an extremely heterogeneous disease of motor neurons that eventually leads to death. Despite impressive advances in understanding the genetic, molecular, and pathological mechanisms of the disease, the only drug approved to date by both the FDA and EMA is riluzole, with a modest effect on survival. In this opinion view paper, we will discuss how to address some challenges for drug development in ALS at the conceptual, technological, and methodological levels. In addition, socioeconomic and ethical issues related to the legitimate need of patients to benefit quickly from new treatments will also be addressed. In conclusion, this brief review takes a more optimistic view, given the recent approval of two new drugs in some countries and the development of targeted gene therapies.
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spelling pubmed-96054582022-10-27 Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas Khamaysa, Mohammed Pradat, Pierre-François J Pers Med Review Amyotrophic lateral sclerosis (ALS) is an extremely heterogeneous disease of motor neurons that eventually leads to death. Despite impressive advances in understanding the genetic, molecular, and pathological mechanisms of the disease, the only drug approved to date by both the FDA and EMA is riluzole, with a modest effect on survival. In this opinion view paper, we will discuss how to address some challenges for drug development in ALS at the conceptual, technological, and methodological levels. In addition, socioeconomic and ethical issues related to the legitimate need of patients to benefit quickly from new treatments will also be addressed. In conclusion, this brief review takes a more optimistic view, given the recent approval of two new drugs in some countries and the development of targeted gene therapies. MDPI 2022-09-28 /pmc/articles/PMC9605458/ /pubmed/36294741 http://dx.doi.org/10.3390/jpm12101601 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Khamaysa, Mohammed
Pradat, Pierre-François
Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title_full Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title_fullStr Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title_full_unstemmed Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title_short Status of ALS Treatment, Insights into Therapeutic Challenges and Dilemmas
title_sort status of als treatment, insights into therapeutic challenges and dilemmas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605458/
https://www.ncbi.nlm.nih.gov/pubmed/36294741
http://dx.doi.org/10.3390/jpm12101601
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