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Clinical trials of new drugs for Alzheimer disease
Alzheimer disease (AD) accounts for 60–70% of dementia cases. Given the seriousness of the disease and continual increase in patient numbers, developing effective therapies to treat AD has become urgent. Presently, the drugs available for AD treatment, including cholinesterase inhibitors and an anta...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943903/ https://www.ncbi.nlm.nih.gov/pubmed/31906949 http://dx.doi.org/10.1186/s12929-019-0609-7 |
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author | Huang, Li-Kai Chao, Shu-Ping Hu, Chaur-Jong |
author_facet | Huang, Li-Kai Chao, Shu-Ping Hu, Chaur-Jong |
author_sort | Huang, Li-Kai |
collection | PubMed |
description | Alzheimer disease (AD) accounts for 60–70% of dementia cases. Given the seriousness of the disease and continual increase in patient numbers, developing effective therapies to treat AD has become urgent. Presently, the drugs available for AD treatment, including cholinesterase inhibitors and an antagonist of the N-methyl-D-aspartate receptor, can only inhibit dementia symptoms for a limited period of time but cannot stop or reverse disease progression. On the basis of the amyloid hypothesis, many global drug companies have conducted many clinical trials on amyloid clearing therapy but without success. Thus, the amyloid hypothesis may not be completely feasible. The number of anti-amyloid trials decreased in 2019, which might be a turning point. An in-depth and comprehensive understanding of the contribution of amyloid beta and other factors of AD is crucial for developing novel pharmacotherapies. In ongoing clinical trials, researchers have developed and are testing several possible interventions aimed at various targets, including anti-amyloid and anti-tau interventions, neurotransmitter modification, anti-neuroinflammation and neuroprotection interventions, and cognitive enhancement, and interventions to relieve behavioral psychological symptoms. In this article, we present the current state of clinical trials for AD at clinicaltrials.gov. We reviewed the underlying mechanisms of these trials, tried to understand the reason why prior clinical trials failed, and analyzed the future trend of AD clinical trials. |
format | Online Article Text |
id | pubmed-6943903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69439032020-01-07 Clinical trials of new drugs for Alzheimer disease Huang, Li-Kai Chao, Shu-Ping Hu, Chaur-Jong J Biomed Sci Review Alzheimer disease (AD) accounts for 60–70% of dementia cases. Given the seriousness of the disease and continual increase in patient numbers, developing effective therapies to treat AD has become urgent. Presently, the drugs available for AD treatment, including cholinesterase inhibitors and an antagonist of the N-methyl-D-aspartate receptor, can only inhibit dementia symptoms for a limited period of time but cannot stop or reverse disease progression. On the basis of the amyloid hypothesis, many global drug companies have conducted many clinical trials on amyloid clearing therapy but without success. Thus, the amyloid hypothesis may not be completely feasible. The number of anti-amyloid trials decreased in 2019, which might be a turning point. An in-depth and comprehensive understanding of the contribution of amyloid beta and other factors of AD is crucial for developing novel pharmacotherapies. In ongoing clinical trials, researchers have developed and are testing several possible interventions aimed at various targets, including anti-amyloid and anti-tau interventions, neurotransmitter modification, anti-neuroinflammation and neuroprotection interventions, and cognitive enhancement, and interventions to relieve behavioral psychological symptoms. In this article, we present the current state of clinical trials for AD at clinicaltrials.gov. We reviewed the underlying mechanisms of these trials, tried to understand the reason why prior clinical trials failed, and analyzed the future trend of AD clinical trials. BioMed Central 2020-01-06 /pmc/articles/PMC6943903/ /pubmed/31906949 http://dx.doi.org/10.1186/s12929-019-0609-7 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Huang, Li-Kai Chao, Shu-Ping Hu, Chaur-Jong Clinical trials of new drugs for Alzheimer disease |
title | Clinical trials of new drugs for Alzheimer disease |
title_full | Clinical trials of new drugs for Alzheimer disease |
title_fullStr | Clinical trials of new drugs for Alzheimer disease |
title_full_unstemmed | Clinical trials of new drugs for Alzheimer disease |
title_short | Clinical trials of new drugs for Alzheimer disease |
title_sort | clinical trials of new drugs for alzheimer disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943903/ https://www.ncbi.nlm.nih.gov/pubmed/31906949 http://dx.doi.org/10.1186/s12929-019-0609-7 |
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