Serveur d'exploration sur la maladie de Parkinson

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Drug repositioning for Alzheimer's disease

Identifieur interne : 000438 ( Main/Curation ); précédent : 000437; suivant : 000439

Drug repositioning for Alzheimer's disease

Auteurs : Anne Corbett [Royaume-Uni] ; James Pickett [Royaume-Uni] ; Alistair Burns [Royaume-Uni] ; Jonathan Corcoran [Royaume-Uni] ; Stephen B. Dunnett [Royaume-Uni] ; Paul Edison [Royaume-Uni] ; Jim J. Hagan [Royaume-Uni] ; Clive Holmes [Royaume-Uni] ; Emma Jones [Royaume-Uni] ; Cornelius Katona [Royaume-Uni] ; Ian Kearns [Royaume-Uni] ; Patrick Kehoe [Royaume-Uni] ; Amrit Mudher [Royaume-Uni] ; Anthony Passmore [Royaume-Uni] ; Nicola Shepherd [Royaume-Uni] ; Frank Walsh [Royaume-Uni] ; Clive Ballard [Royaume-Uni]

Source :

RBID : ISTEX:6A37E13CBEAD425373FA2EBBB3598916D2A6A7DB

Abstract

Existing drugs for Alzheimer's disease provide symptomatic benefit for up to 12 months, but there are no approved disease-modifying therapies. Given the recent failures of various novel disease-modifying therapies in clinical trials, a complementary strategy based on repositioning drugs that are approved for other indications could be attractive. Indeed, a substantial body of preclinical work indicates that several classes of such drugs have potentially beneficial effects on Alzheimer's-like brain pathology, and for some drugs the evidence is also supported by epidemiological data or preliminary clinical trials. Here, we present a formal consensus evaluation of these opportunities, based on a systematic review of published literature. We highlight several compounds for which sufficient evidence is available to encourage further investigation to clarify an optimal dose and consider progression to clinical trials in patients with Alzheimer's disease.

Url:
DOI: 10.1038/nrd3869

Links toward previous steps (curation, corpus...)


Links to Exploration step

ISTEX:6A37E13CBEAD425373FA2EBBB3598916D2A6A7DB

Curation

No country items

Anne Corbett
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James Pickett
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<mods:affiliation>A.C. and J.P. contributed equally to this work.</mods:affiliation>
<wicri:noCountry code="no comma">A.C. and J.P. contributed equally to this work.</wicri:noCountry>
</affiliation>

Le document en format XML

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<name sortKey="Ballard, Clive" sort="Ballard, Clive" uniqKey="Ballard C" first="Clive" last="Ballard">Clive Ballard</name>
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<name sortKey="Passmore, Anthony" sort="Passmore, Anthony" uniqKey="Passmore A" first="Anthony" last="Passmore">Anthony Passmore</name>
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<wicri:regionArea>Anthony Passmore is at Queen's University Belfast, Centre for Public Health, Whitla Medical Building, 97 Lisburn Road, Belfast BT9 7BL</wicri:regionArea>
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<name sortKey="Shepherd, Nicola" sort="Shepherd, Nicola" uniqKey="Shepherd N" first="Nicola" last="Shepherd">Nicola Shepherd</name>
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<country xml:lang="fr" wicri:curation="lc">Royaume-Uni</country>
<wicri:regionArea>Nicola Shepherd is at the Wellcome Trust, Gibbs Building, 215 Euston Road, London NW1 2BE</wicri:regionArea>
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<name sortKey="Walsh, Frank" sort="Walsh, Frank" uniqKey="Walsh F" first="Frank" last="Walsh">Frank Walsh</name>
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<mods:affiliation>Frank Walsh is at the Institute of Psychiatry, King's College London, London SE1 1UL, UK.</mods:affiliation>
<country xml:lang="fr" wicri:curation="lc">Royaume-Uni</country>
<wicri:regionArea>Frank Walsh is at the Institute of Psychiatry, King's College London, London SE1 1UL</wicri:regionArea>
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<name sortKey="Ballard, Clive" sort="Ballard, Clive" uniqKey="Ballard C" first="Clive" last="Ballard">Clive Ballard</name>
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<wicri:regionArea>Anne Corbett and Clive Ballard are at the Wolfson Centre for Age-Related Diseases, King's College London, London SE1 1UL</wicri:regionArea>
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<title level="j">Nature Reviews Drug Discovery</title>
<idno type="ISSN">1474-1776</idno>
<idno type="eISSN">1474-1784</idno>
<imprint>
<publisher>Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.</publisher>
<date type="published" when="2012-11">2012-11</date>
<biblScope unit="volume">11</biblScope>
<biblScope unit="issue">11</biblScope>
<biblScope unit="page" from="833">833</biblScope>
<biblScope unit="page" to="846">846</biblScope>
</imprint>
<idno type="ISSN">1474-1776</idno>
</series>
<idno type="istex">6A37E13CBEAD425373FA2EBBB3598916D2A6A7DB</idno>
<idno type="DOI">10.1038/nrd3869</idno>
<idno type="ArticleID">nrd3869</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">1474-1776</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="eng">Existing drugs for Alzheimer's disease provide symptomatic benefit for up to 12 months, but there are no approved disease-modifying therapies. Given the recent failures of various novel disease-modifying therapies in clinical trials, a complementary strategy based on repositioning drugs that are approved for other indications could be attractive. Indeed, a substantial body of preclinical work indicates that several classes of such drugs have potentially beneficial effects on Alzheimer's-like brain pathology, and for some drugs the evidence is also supported by epidemiological data or preliminary clinical trials. Here, we present a formal consensus evaluation of these opportunities, based on a systematic review of published literature. We highlight several compounds for which sufficient evidence is available to encourage further investigation to clarify an optimal dose and consider progression to clinical trials in patients with Alzheimer's disease.</div>
</front>
</TEI>
</record>

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