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Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial

OBJECTIVE: To assess the efficacy, safety, and tolerability of adjunctive levetiracetam (LEV) in Chinese and Japanese adults with generalized tonic–clonic (GTC) seizures (N01159; NCT01228747). METHODS: This double‐blind, randomized, placebo‐controlled, multicenter phase III trial comprised: 4‐week r...

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Autores principales: Wu, Liwen, Yagi, Kazuichi, Hong, Zhen, Liao, Weiping, Wang, Xuefeng, Zhou, Dong, Inoue, Yushi, Ohtsuka, Yoko, Sasagawa, Mutsuo, Terada, Kiyohito, Du, Xinlu, Muramoto, Yoshihiro, Sano, Tomonobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276779/
https://www.ncbi.nlm.nih.gov/pubmed/30525116
http://dx.doi.org/10.1002/epi4.12255
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author Wu, Liwen
Yagi, Kazuichi
Hong, Zhen
Liao, Weiping
Wang, Xuefeng
Zhou, Dong
Inoue, Yushi
Ohtsuka, Yoko
Sasagawa, Mutsuo
Terada, Kiyohito
Du, Xinlu
Muramoto, Yoshihiro
Sano, Tomonobu
author_facet Wu, Liwen
Yagi, Kazuichi
Hong, Zhen
Liao, Weiping
Wang, Xuefeng
Zhou, Dong
Inoue, Yushi
Ohtsuka, Yoko
Sasagawa, Mutsuo
Terada, Kiyohito
Du, Xinlu
Muramoto, Yoshihiro
Sano, Tomonobu
author_sort Wu, Liwen
collection PubMed
description OBJECTIVE: To assess the efficacy, safety, and tolerability of adjunctive levetiracetam (LEV) in Chinese and Japanese adults with generalized tonic–clonic (GTC) seizures (N01159; NCT01228747). METHODS: This double‐blind, randomized, placebo‐controlled, multicenter phase III trial comprised: 4‐week retrospective and 4‐week prospective baseline, 12‐week dose‐adjustment, and 16‐week evaluation periods. Chinese and Japanese patients ≥16 years old with idiopathic generalized, symptomatic generalized, or undetermined epilepsy with GTC seizures received a single‐blind placebo during the prospective baseline, and then were randomized 1:1 to placebo or LEV 1,000 mg/day administered twice daily. Patients reporting GTC seizures up to week 8 had the LEV dosage increased to 3,000 mg/day. The primary efficacy variable was percent reduction from combined baseline in GTC seizures/week during the 28‐week treatment period. RESULTS: Overall, 251 patients were randomized (208 from China; 43 from Japan); 141 (56.2%) completed the 28‐week treatment period. Least‐squares mean percent reduction from combined baseline in GTC seizures/week (treatment period) was placebo 12.6% versus LEV 68.8% (95% confidence interval, 44.0–68.2; p < 0.0001). GTC seizure frequency reduction occurred in both patients with idiopathic and symptomatic generalized epilepsy. The 50% responder rate (treatment period) was placebo 28.4% versus LEV 77.8%. Freedom from GTC seizures (evaluation period) was placebo 3.1% versus LEV 29.6%. Incidence of treatment‐emergent adverse events (TEAEs; treatment period) was placebo 52.0% versus LEV 57.1%; most frequently nasopharyngitis, protein in urine, decreased platelet count, and pyrexia. Incidence of TEAEs leading to discontinuation was 4.8% versus 3.2%; incidence of serious TEAEs was 3.2% versus 0.8% for placebo and LEV, respectively; 3 patients taking placebo died versus none taking LEV. SIGNIFICANCE: In this trial, adjunctive LEV 1,000–3,000 mg/day was effective in reducing GTC seizure frequency in Chinese and Japanese patients ≥16 years old with GTC seizures. Seizure reduction occurred in both patients with idiopathic and symptomatic generalized epilepsy. LEV was well tolerated in this population.
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spelling pubmed-62767792018-12-06 Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial Wu, Liwen Yagi, Kazuichi Hong, Zhen Liao, Weiping Wang, Xuefeng Zhou, Dong Inoue, Yushi Ohtsuka, Yoko Sasagawa, Mutsuo Terada, Kiyohito Du, Xinlu Muramoto, Yoshihiro Sano, Tomonobu Epilepsia Open Full‐length Original Research OBJECTIVE: To assess the efficacy, safety, and tolerability of adjunctive levetiracetam (LEV) in Chinese and Japanese adults with generalized tonic–clonic (GTC) seizures (N01159; NCT01228747). METHODS: This double‐blind, randomized, placebo‐controlled, multicenter phase III trial comprised: 4‐week retrospective and 4‐week prospective baseline, 12‐week dose‐adjustment, and 16‐week evaluation periods. Chinese and Japanese patients ≥16 years old with idiopathic generalized, symptomatic generalized, or undetermined epilepsy with GTC seizures received a single‐blind placebo during the prospective baseline, and then were randomized 1:1 to placebo or LEV 1,000 mg/day administered twice daily. Patients reporting GTC seizures up to week 8 had the LEV dosage increased to 3,000 mg/day. The primary efficacy variable was percent reduction from combined baseline in GTC seizures/week during the 28‐week treatment period. RESULTS: Overall, 251 patients were randomized (208 from China; 43 from Japan); 141 (56.2%) completed the 28‐week treatment period. Least‐squares mean percent reduction from combined baseline in GTC seizures/week (treatment period) was placebo 12.6% versus LEV 68.8% (95% confidence interval, 44.0–68.2; p < 0.0001). GTC seizure frequency reduction occurred in both patients with idiopathic and symptomatic generalized epilepsy. The 50% responder rate (treatment period) was placebo 28.4% versus LEV 77.8%. Freedom from GTC seizures (evaluation period) was placebo 3.1% versus LEV 29.6%. Incidence of treatment‐emergent adverse events (TEAEs; treatment period) was placebo 52.0% versus LEV 57.1%; most frequently nasopharyngitis, protein in urine, decreased platelet count, and pyrexia. Incidence of TEAEs leading to discontinuation was 4.8% versus 3.2%; incidence of serious TEAEs was 3.2% versus 0.8% for placebo and LEV, respectively; 3 patients taking placebo died versus none taking LEV. SIGNIFICANCE: In this trial, adjunctive LEV 1,000–3,000 mg/day was effective in reducing GTC seizure frequency in Chinese and Japanese patients ≥16 years old with GTC seizures. Seizure reduction occurred in both patients with idiopathic and symptomatic generalized epilepsy. LEV was well tolerated in this population. John Wiley and Sons Inc. 2018-09-29 /pmc/articles/PMC6276779/ /pubmed/30525116 http://dx.doi.org/10.1002/epi4.12255 Text en © 2018 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full‐length Original Research
Wu, Liwen
Yagi, Kazuichi
Hong, Zhen
Liao, Weiping
Wang, Xuefeng
Zhou, Dong
Inoue, Yushi
Ohtsuka, Yoko
Sasagawa, Mutsuo
Terada, Kiyohito
Du, Xinlu
Muramoto, Yoshihiro
Sano, Tomonobu
Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title_full Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title_fullStr Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title_full_unstemmed Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title_short Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial
title_sort adjunctive levetiracetam in the treatment of chinese and japanese adults with generalized tonic–clonic seizures: a double‐blind, randomized, placebo‐controlled trial
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276779/
https://www.ncbi.nlm.nih.gov/pubmed/30525116
http://dx.doi.org/10.1002/epi4.12255
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