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Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease

Alzheimer’s Disease (AD) is the most common cause of dementia, affecting approximately two thirds of the 35 million people worldwide with the condition. Despite this, effective treatments are lacking, and there are no drugs that elicit disease modifying effects to improve outcome. There is an urgent...

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Detalles Bibliográficos
Autores principales: Corbett, Anne, Williams, Gareth, Ballard, Clive
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817602/
https://www.ncbi.nlm.nih.gov/pubmed/24275851
http://dx.doi.org/10.3390/ph6101304
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author Corbett, Anne
Williams, Gareth
Ballard, Clive
author_facet Corbett, Anne
Williams, Gareth
Ballard, Clive
author_sort Corbett, Anne
collection PubMed
description Alzheimer’s Disease (AD) is the most common cause of dementia, affecting approximately two thirds of the 35 million people worldwide with the condition. Despite this, effective treatments are lacking, and there are no drugs that elicit disease modifying effects to improve outcome. There is an urgent need to develop and evaluate more effective pharmacological treatments. Drug repositioning offers an exciting opportunity to repurpose existing licensed treatments for use in AD, with the benefit of providing a far more rapid route to the clinic than through novel drug discovery approaches. This review outlines the current most promising candidates for repositioning in AD, their supporting evidence and their progress through trials to date. Furthermore, it begins to explore the potential of new transcriptomic and microarray techniques to consider the future of drug repositioning as a viable approach to drug discovery.
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spelling pubmed-38176022013-11-14 Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease Corbett, Anne Williams, Gareth Ballard, Clive Pharmaceuticals (Basel) Review Alzheimer’s Disease (AD) is the most common cause of dementia, affecting approximately two thirds of the 35 million people worldwide with the condition. Despite this, effective treatments are lacking, and there are no drugs that elicit disease modifying effects to improve outcome. There is an urgent need to develop and evaluate more effective pharmacological treatments. Drug repositioning offers an exciting opportunity to repurpose existing licensed treatments for use in AD, with the benefit of providing a far more rapid route to the clinic than through novel drug discovery approaches. This review outlines the current most promising candidates for repositioning in AD, their supporting evidence and their progress through trials to date. Furthermore, it begins to explore the potential of new transcriptomic and microarray techniques to consider the future of drug repositioning as a viable approach to drug discovery. MDPI 2013-10-11 /pmc/articles/PMC3817602/ /pubmed/24275851 http://dx.doi.org/10.3390/ph6101304 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Corbett, Anne
Williams, Gareth
Ballard, Clive
Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title_full Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title_fullStr Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title_full_unstemmed Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title_short Drug Repositioning: An Opportunity to Develop Novel Treatments for Alzheimer’s Disease
title_sort drug repositioning: an opportunity to develop novel treatments for alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817602/
https://www.ncbi.nlm.nih.gov/pubmed/24275851
http://dx.doi.org/10.3390/ph6101304
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