Cited by 467Epilepsy research and treatmentPharmacological Effects and Toxicity StudiesDiet and metabolism studies

Comparison of levetiracetam and controlled-release carbamazepine in newly diagnosed epilepsy

Brodie, M. J., Perucca, E., Ryvlin, P., Ben-Menachem, E., Meencke, H.-J·2007·Neurology

Abstract

Objective We report the results of a prospective study of the efficacy and tolerability of levetiracetam, a new antiepileptic drug with a unique mechanism of action, in comparison with controlled-release carbamazepine as first treatment in newly diagnosed epilepsy. Methods Adults with > or =2 partial or generalized tonic-clonic seizures in the previous year were randomly assigned to levetiracetam (500 mg twice daily, n = 288) or controlled-release carbamazepine (200 mg twice daily, n = 291) in a multicenter, double-blind, noninferiority, parallel-group trial. If a seizure occurred within 26 weeks of stabilization, dosage was increased incrementally to a maximum of levetiracetam 1,500 mg twice daily or carbamazepine 600 mg twice daily. Patients achieving the primary endpoint (6-month seizure freedom) continued on treatment for a further 6-month maintenance period. Results At per-protocol analysis, 73.0% (56.6%) of patients randomized to levetiracetam and 72.8% (58.5%) receiving controlled-release carbamazepine were seizure free at the last evaluated dose (adjusted absolute difference 0.2%, 95% CI -7.8% to 8.2%) for > or =6 months (1 year). Of all patients achieving 6-month (1-year) remission, 80.1% (86.0%) in the levetiracetam group and 85.4% (89.3%) in the carbamazepine group did so at the lowest dose level. Withdrawal rates for adverse events were 14.4% with levetiracetam and 19.2% with carbamazepine. Conclusions Levetiracetam and controlled-release carbamazepine produced eq…

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Crossref · 10.1212/01.wnl.0000252941.50833.4a

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Authors
Brodie, M. J., Perucca, E., Ryvlin, P., Ben-Menachem, E., & Meencke, H.-J.
Affiliations
  • University of Pavia (IT)
  • From the Epilepsy Unit, Western Infirmary, Glasgow, Scotland (M.J.B.); Institute of Neurology, IRCCS C, Mondino Foundation and Clinical Pharmacology Unit, University of Pavia, Pavia, Italy (E.P.); Hospices Civils de Lyon, Lyon, France (P.R.); Sahlgren University Hospital, Göteborg, Sweden (E.B.-M.); and Epilepsy Centre of Berlin, Berlin, Germany (H.-J.M.).
Venue
Neurology
Published
2007-02-06
Volume
68
Issue
6
Pages
402-408
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2028500192
Cited by
467
References
1
Citations by year
2026: 9 · 2025: 8 · 2024: 7 · 2023: 7 · 2022: 13 · 2021: 19 · 2020: 51 · 2019: 16 · 2018: 22 · 2017: 25 · 2016: 17 · 2015: 28 · 2014: 21 · 2013: 24 · 2012: 39
FWCI
24.51
Type
journal article
Language
en
Open access
closed
Locations
  • Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
  • Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) (submittedVersion)
Funders
Union Chimique Belge
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmacological Effects and Toxicity Studies
  • Health Sciences › Medicine › Physiology › Diet and metabolism studies
Keywords
levetiracetam, newly diagnosed epilepsy, seizure freedom, antiepileptic drugs, first-line therapy, focal seizures, generalized tonic-clonic seizures, drug tolerability, dose optimization
MeSH terms
Levetiracetam, Adult, Anticonvulsants, Carbamazepine, Delayed-Action Preparations, Dose-Response Relationship, Drug, Double-Blind Method, Epilepsy, Female, Humans, Male, Piracetam, Treatment Outcome

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