KRAUSS, G.L., M. BAR, V. BITON, J.A. KLAPPER, Ivan REKTOR, N. VAICIENE-MAGISTRIS, D. SQUILLACOTE a Dwijendra Kumar GUPTA. Tolerability and safety of perampanel: two randomized dose-escalation studies. Acta Neurologica Scandinavica. MALDEN: WILEY-BLACKWELL, 2012, roč. 125, č. 1, s. 8-15. ISSN 0001-6314. doi:10.1111/j.1600-0404.2011.01588.x.
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Základní údaje
Originální název Tolerability and safety of perampanel: two randomized dose-escalation studies
Autoři KRAUSS, G.L., M. BAR, V. BITON, J.A. KLAPPER, Ivan REKTOR, N. VAICIENE-MAGISTRIS, D. SQUILLACOTE a Dwijendra Kumar GUPTA.
Vydání Acta Neurologica Scandinavica, MALDEN, WILEY-BLACKWELL, 2012, 0001-6314.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30000 3. Medical and Health Sciences
Stát vydavatele Dánsko
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.474
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/j.1600-0404.2011.01588.x
UT WoS 000298477600005
Klíčová slova anglicky antiepileptic drugs; efficacy; partial-onset; perampanel; refractory; safety
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 23. 4. 2014 14:12.
Anotace
Objectives - 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. Materials and methods - Two consecutive, randomized, double-blind, dose-escalation studies recruited adults (18-70 years) with uncontrolled partial-onset seizures receiving one to three concomitant antiepileptic drugs. In study 206, patients were treated for 12 weeks (8-week dose-titration, 4-week dose-maintenance) with placebo or perampanel (up to 4 mg/day, dosed once-or twice-daily). In study 208, patients received placebo or perampanel once-daily (up to 12 mg) for 16 weeks (12-week titration, 4-week maintenance). Results - Overall, 153 patients were randomized into study 206 (perampanel twice-daily, n = 51; perampanel once-daily, n = 51; placebo, n = 51). Study 208 included 48 patients (perampanel once-daily, n = 38; placebo, n = 10). The highest dose in study 206 - 4 mg/day - was well tolerated, with similar proportions of patients tolerating once-daily (82.4%) and twice-daily (82.4%) perampanel and placebo (82.4%) treatments. In study 208 most patients tolerated doses of 6 mg perampanel once-daily in a Kaplan-Meier analysis. In both studies, the most common adverse events were CNS-related; most were of mild/moderate severity. Conclusions Perampanel was well tolerated across doses of 4-12 mg/day. The studies showed preliminary evidence of efficacy and identified doses to be evaluated in larger clinical studies.
VytisknoutZobrazeno: 16. 5. 2022 14:48