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Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β

The failure of several potential Alzheimer’s disease therapeutics in mid- to late-stage clinical development has provoked significant discussion regarding the validity of the amyloid hypothesis. In this review, we propose a minimum criterion of 25% for amyloid-β (Aβ) lowering to achieve clinically m...

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Detalles Bibliográficos
Autores principales: Toyn, Jeremy H, Ahlijanian, Michael K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014014/
https://www.ncbi.nlm.nih.gov/pubmed/25031632
http://dx.doi.org/10.1186/alzrt244
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author Toyn, Jeremy H
Ahlijanian, Michael K
author_facet Toyn, Jeremy H
Ahlijanian, Michael K
author_sort Toyn, Jeremy H
collection PubMed
description The failure of several potential Alzheimer’s disease therapeutics in mid- to late-stage clinical development has provoked significant discussion regarding the validity of the amyloid hypothesis. In this review, we propose a minimum criterion of 25% for amyloid-β (Aβ) lowering to achieve clinically meaningful slowing of disease progression. This criterion is based on genetic, risk factor, clinical and preclinical studies. We then compare this minimum criterion with the degree of Aβ lowering produced by the potential therapies that have failed in clinical trials. If the proposed minimum Aβ lowering criterion is used, then the amyloid hypothesis has yet to be adequately tested in the clinic. Therefore, we believe that the amyloid hypothesis remains valid and remains to be confirmed or refuted in future clinical trials.
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spelling pubmed-40140142015-03-12 Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β Toyn, Jeremy H Ahlijanian, Michael K Alzheimers Res Ther Review The failure of several potential Alzheimer’s disease therapeutics in mid- to late-stage clinical development has provoked significant discussion regarding the validity of the amyloid hypothesis. In this review, we propose a minimum criterion of 25% for amyloid-β (Aβ) lowering to achieve clinically meaningful slowing of disease progression. This criterion is based on genetic, risk factor, clinical and preclinical studies. We then compare this minimum criterion with the degree of Aβ lowering produced by the potential therapies that have failed in clinical trials. If the proposed minimum Aβ lowering criterion is used, then the amyloid hypothesis has yet to be adequately tested in the clinic. Therefore, we believe that the amyloid hypothesis remains valid and remains to be confirmed or refuted in future clinical trials. BioMed Central 2014-03-12 /pmc/articles/PMC4014014/ /pubmed/25031632 http://dx.doi.org/10.1186/alzrt244 Text en Copyright © 2014 Toyn and Ahlijanian; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Toyn, Jeremy H
Ahlijanian, Michael K
Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title_full Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title_fullStr Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title_full_unstemmed Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title_short Interpreting Alzheimer’s disease clinical trials in light of the effects on amyloid-β
title_sort interpreting alzheimer’s disease clinical trials in light of the effects on amyloid-β
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014014/
https://www.ncbi.nlm.nih.gov/pubmed/25031632
http://dx.doi.org/10.1186/alzrt244
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