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Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures
OBJECTIVE: To evaluate the efficacy and safety of adjunctive cenobamate 200 mg/d in patients with uncontrolled focal (partial-onset) seizures despite treatment with 1 to 3 antiepileptic drugs. METHODS: In this multicenter, double-blind, placebo-controlled study, adults 18 to 65 years of age with foc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357293/ https://www.ncbi.nlm.nih.gov/pubmed/32409485 http://dx.doi.org/10.1212/WNL.0000000000009530 |
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author | Chung, Steve S. French, Jacqueline A. Kowalski, Jacek Krauss, Gregory L. Lee, Sang Kun Maciejowski, Maciej Rosenfeld, William E. Sperling, Michael R. Mizne, Sarah Kamin, Marc |
author_facet | Chung, Steve S. French, Jacqueline A. Kowalski, Jacek Krauss, Gregory L. Lee, Sang Kun Maciejowski, Maciej Rosenfeld, William E. Sperling, Michael R. Mizne, Sarah Kamin, Marc |
author_sort | Chung, Steve S. |
collection | PubMed |
description | OBJECTIVE: To evaluate the efficacy and safety of adjunctive cenobamate 200 mg/d in patients with uncontrolled focal (partial-onset) seizures despite treatment with 1 to 3 antiepileptic drugs. METHODS: In this multicenter, double-blind, placebo-controlled study, adults 18 to 65 years of age with focal seizures were randomized 1:1 (cenobamate:placebo) after an 8-week baseline period. The 12-week double-blind treatment period consisted of a 6-week titration phase and a 6-week maintenance phase. The primary outcome was percent change in seizure frequency (from baseline) per 28 days during double-blind treatment. RESULTS: Two hundred twenty-two patients were randomized; 113 received cenobamate and 109 received placebo; and 90.3% and 90.8% of patients, respectively, completed double-blind treatment. Median baseline seizure frequency was 6.5 in 28 days (range 0–237). Compared to placebo, cenobamate conferred a greater median percent seizure reduction (55.6% vs 21.5%; p < 0.0001) The responder rate (≥50% reduction in seizure frequency) was 50.4% for cenobamate and 22.2% for placebo (p < 0.0001). Focal seizures with motor component, impaired awareness, and focal to bilateral tonic-clonic seizures were significantly reduced with cenobamate vs placebo. During maintenance, 28.3% of cenobamate-treated and 8.8% of placebo-treated patients were seizure-free. Treatment-emergent adverse events reported in >10% in either group (cenobamate vs placebo) were somnolence (22.1% vs 11.9%), dizziness (22.1% vs 16.5%), headache (12.4% vs 12.8%), nausea (11.5% vs 4.6%), and fatigue (10.6% vs 6.4%). CONCLUSION: Adjunctive treatment with cenobamate 200 mg/d significantly improved seizure control in adults with uncontrolled focal seizures and was well tolerated. CLINICALTRIALS.GOV IDENTIFIER: NCT01397968. CLASSIFICATION OF EVIDENCE: This study provides Class I evidence that, for patients with uncontrolled focal seizures, adjunctive cenobamate reduces seizures. |
format | Online Article Text |
id | pubmed-7357293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-73572932020-08-03 Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures Chung, Steve S. French, Jacqueline A. Kowalski, Jacek Krauss, Gregory L. Lee, Sang Kun Maciejowski, Maciej Rosenfeld, William E. Sperling, Michael R. Mizne, Sarah Kamin, Marc Neurology Article OBJECTIVE: To evaluate the efficacy and safety of adjunctive cenobamate 200 mg/d in patients with uncontrolled focal (partial-onset) seizures despite treatment with 1 to 3 antiepileptic drugs. METHODS: In this multicenter, double-blind, placebo-controlled study, adults 18 to 65 years of age with focal seizures were randomized 1:1 (cenobamate:placebo) after an 8-week baseline period. The 12-week double-blind treatment period consisted of a 6-week titration phase and a 6-week maintenance phase. The primary outcome was percent change in seizure frequency (from baseline) per 28 days during double-blind treatment. RESULTS: Two hundred twenty-two patients were randomized; 113 received cenobamate and 109 received placebo; and 90.3% and 90.8% of patients, respectively, completed double-blind treatment. Median baseline seizure frequency was 6.5 in 28 days (range 0–237). Compared to placebo, cenobamate conferred a greater median percent seizure reduction (55.6% vs 21.5%; p < 0.0001) The responder rate (≥50% reduction in seizure frequency) was 50.4% for cenobamate and 22.2% for placebo (p < 0.0001). Focal seizures with motor component, impaired awareness, and focal to bilateral tonic-clonic seizures were significantly reduced with cenobamate vs placebo. During maintenance, 28.3% of cenobamate-treated and 8.8% of placebo-treated patients were seizure-free. Treatment-emergent adverse events reported in >10% in either group (cenobamate vs placebo) were somnolence (22.1% vs 11.9%), dizziness (22.1% vs 16.5%), headache (12.4% vs 12.8%), nausea (11.5% vs 4.6%), and fatigue (10.6% vs 6.4%). CONCLUSION: Adjunctive treatment with cenobamate 200 mg/d significantly improved seizure control in adults with uncontrolled focal seizures and was well tolerated. CLINICALTRIALS.GOV IDENTIFIER: NCT01397968. CLASSIFICATION OF EVIDENCE: This study provides Class I evidence that, for patients with uncontrolled focal seizures, adjunctive cenobamate reduces seizures. Lippincott Williams & Wilkins 2020-06-02 /pmc/articles/PMC7357293/ /pubmed/32409485 http://dx.doi.org/10.1212/WNL.0000000000009530 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Chung, Steve S. French, Jacqueline A. Kowalski, Jacek Krauss, Gregory L. Lee, Sang Kun Maciejowski, Maciej Rosenfeld, William E. Sperling, Michael R. Mizne, Sarah Kamin, Marc Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title | Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title_full | Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title_fullStr | Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title_full_unstemmed | Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title_short | Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
title_sort | randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357293/ https://www.ncbi.nlm.nih.gov/pubmed/32409485 http://dx.doi.org/10.1212/WNL.0000000000009530 |
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