Tolerability and safety of perampanel: Two randomized dose-escalation studies
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F12%3AA120147V" target="_blank" >RIV/61988987:17110/12:A120147V - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Tolerability and safety of perampanel: Two randomized dose-escalation studies
Original language description
To evaluate, for the first time in patients with epilepsy, the tolerability and safety of escalating doses of oral perampanel, a novel, selective, non-competitive AMPA antagonist, as adjunctive therapy for refractory partial-onset seizures. Perampanel was well tolerated across doses of 4-12mg/day. The studies showed preliminary evidence of efficacy and identified doses to be evaluated in larger clinical studies
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
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Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
ACTA NEUROL SCAND
ISSN
0001-6314
e-ISSN
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Volume of the periodical
125
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
8
Pages from-to
8-15
UT code for WoS article
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EID of the result in the Scopus database
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