La maladie de Parkinson au Canada (serveur d'exploration)

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Perampanel, an AMPA antagonist, found to have no benefit in reducing “off” time in Parkinson's disease

Identifieur interne : 002320 ( Istex/Corpus ); précédent : 002319; suivant : 002321

Perampanel, an AMPA antagonist, found to have no benefit in reducing “off” time in Parkinson's disease

Auteurs : Andrew Lees ; Stanley Fahn ; Karla M. Eggert ; Joseph Jankovic ; Anthony Lang ; Federico Micheli ; M. Maral Mouradian ; Wolfgang H. Oertel ; C. Warren Olanow ; Werner Poewe ; Olivier Rascol ; Eduardo Tolosa ; David Squillacote ; Dinesh Kumar

Source :

RBID : ISTEX:C8FC6F258A678C36B801D2375E63FFB5F31FC7F3

English descriptors

Abstract

Perampanel is a selective, noncompetitive α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole‐propionic acid receptor antagonist. Two multicenter randomized, double‐blind, placebo‐controlled, parallel‐group phase III studies assessed the efficacy and safety of adjunctive perampanel in patients with Parkinson's disease and motor fluctuations.

Url:
DOI: 10.1002/mds.23983

Links to Exploration step

ISTEX:C8FC6F258A678C36B801D2375E63FFB5F31FC7F3

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<div type="abstract">Perampanel is a selective, noncompetitive α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole‐propionic acid receptor antagonist. Two multicenter randomized, double‐blind, placebo‐controlled, parallel‐group phase III studies assessed the efficacy and safety of adjunctive perampanel in patients with Parkinson's disease and motor fluctuations.</div>
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<note type="content">*Funding agencies: These studies were funded by Eisai Inc.</note>
<note type="content">*Relevant conflicts of interest/financial disclosures: All authors received compensation from Eisai for their site's conduct of the study and/or as members of steering committees. Joseph Jankovic has received honoraria as a consultant to Eisai. Anthony Lang, M. Maral Mouradian, Olivier Rascol, and C. Warren Olanow have served as advisers or consultants for Eisai. David Squillacote and Dinesh Kumar are employed by Eisai.</note>
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<b>Funding agencies:</b>
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<b>Relevant conflicts of interest/financial disclosures:</b>
All authors received compensation from Eisai for their site's conduct of the study and/or as members of steering committees. Joseph Jankovic has received honoraria as a consultant to Eisai. Anthony Lang, M. Maral Mouradian, Olivier Rascol, and C. Warren Olanow have served as advisers or consultants for Eisai. David Squillacote and Dinesh Kumar are employed by Eisai.</p>
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<abstract>Perampanel is a selective, noncompetitive α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole‐propionic acid receptor antagonist. Two multicenter randomized, double‐blind, placebo‐controlled, parallel‐group phase III studies assessed the efficacy and safety of adjunctive perampanel in patients with Parkinson's disease and motor fluctuations.</abstract>
<abstract>In both phase III studies (301 and 302), levodopa‐treated patients were randomized and treated with once‐daily oral placebo (n = 504), perampanel 2 mg (n = 509), or perampanel 4 mg (n = 501). The primary end point was change in daily “off” time from baseline. The treatment period was 30 weeks in study 301 and 20 weeks in study 302.</abstract>
<abstract>For any efficacy end point, perampanel 2 or 4 mg was not superior to placebo. Perampanel was well tolerated up to 4 mg/day.</abstract>
<abstract>Perampanel failed to significantly improve motor symptoms versus placebo. There was also no effect on the duration or disability of levodopa‐induced dyskinesia. © 2011 Movement Disorder Society</abstract>
<note type="content">*Funding agencies: These studies were funded by Eisai Inc.</note>
<note type="content">*Relevant conflicts of interest/financial disclosures: All authors received compensation from Eisai for their site's conduct of the study and/or as members of steering committees. Joseph Jankovic has received honoraria as a consultant to Eisai. Anthony Lang, M. Maral Mouradian, Olivier Rascol, and C. Warren Olanow have served as advisers or consultants for Eisai. David Squillacote and Dinesh Kumar are employed by Eisai.</note>
<note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note>
<subject lang="en">
<genre>keywords</genre>
<topic>AMPA receptor antagonist</topic>
<topic>efficacy</topic>
<topic>motor fluctuations</topic>
<topic>Parkinson's disease</topic>
<topic>perampanel</topic>
<topic>safety</topic>
</subject>
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<titleInfo>
<title>Movement Disorders</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Brief Report</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2012</date>
<detail type="volume">
<caption>vol.</caption>
<number>27</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>2</number>
</detail>
<extent unit="pages">
<start>284</start>
<end>288</end>
<total>5</total>
</extent>
</part>
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<identifier type="istex">C8FC6F258A678C36B801D2375E63FFB5F31FC7F3</identifier>
<identifier type="DOI">10.1002/mds.23983</identifier>
<identifier type="ArticleID">MDS23983</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 Movement Disorder Society</accessCondition>
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<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
</recordInfo>
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<serie></serie>
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