Serveur d'exploration autour de Joseph Jankovic

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

Identifieur interne : 000350 ( Ncbi/Merge ); précédent : 000349; suivant : 000351

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

Auteurs : Andrew Lees [Royaume-Uni] ; Stanley Fahn ; Karla. Eggert ; Joseph Jankovic [États-Unis] ; Anthony Lang ; Federico Micheli ; M Mouradian ; Wolfgang. Oertel ; C Olanow ; Werner Poewe ; Olivier Rascol ; Eduardo Tolosa ; David Squillacote ; Dinesh Kumar

Source :

RBID : pubmed:22161845

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.

DOI: 10.1002/mds.23983
PubMed: 22161845

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pubmed:22161845

Le document en format XML

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<div type="abstract" xml:lang="en">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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<DateCreated>
<Year>2012</Year>
<Month>02</Month>
<Day>13</Day>
</DateCreated>
<DateCompleted>
<Year>2012</Year>
<Month>06</Month>
<Day>14</Day>
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<Month>11</Month>
<Day>15</Day>
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<Volume>27</Volume>
<Issue>2</Issue>
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<Month>Feb</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">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.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">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.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">For any efficacy end point, perampanel 2 or 4 mg was not superior to placebo. Perampanel was well tolerated up to 4 mg/day.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Perampanel failed to significantly improve motor symptoms versus placebo. There was also no effect on the duration or disability of levodopa-induced dyskinesia.</AbstractText>
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