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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9605458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT khamaysamohammed statusofalstreatmentinsightsintotherapeuticchallengesanddilemmas AT pradatpierrefrancois statusofalstreatmentinsightsintotherapeuticchallengesanddilemmas |