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Published online before print July 11, 2007, doi:10.1212/01.wnl.0000268699.34614.d3)
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Received February 14, 2007
Accepted April 19, 2007

Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy

S. F. Berkovic MD*, R. C. Knowlton MD, R. F. Leroy MD, J. Schiemann MD, U. Falter PhD, On behalf of the Levetiracetam N01057 Study Group

From the Epilepsy Research Center (S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Australia; UAB Epilepsy Center (R.C.K.), Department of Neurology, University of Alabama at Birmingham School of Medicine; Neurological Clinic of Texas (R.F.L.), Dallas; UCB Inc. (J.S.), Atlanta, GA; and UCB Pharma SA (U.F.), Braine-l’Alleud, Belgium.


* To whom correspondence should be addressed. E-mail: s.berkovic{at}unimelb.edu.au.

Abstract Objective: To assess the efficacy and tolerability of adjunctive levetiracetam in patients with uncontrolled generalized tonic-clonic (GTC) seizures associated with idiopathic generalized epilepsies (IGE).

Methods: This multicenter, randomized, double-blind, placebo-controlled, parallel-group study enrolled adults and children (4 to 65 years) with IGE experiencing ≥3 GTC seizures during the 8-week baseline period (4-week retrospective and 4-week prospective), despite receiving stable doses of one or two antiepileptic drugs (AEDs). Patients were randomized to levetiracetam (target dose 3,000 mg/day for adults; 60 mg/kg/day for children) or placebo and a 4-week titration period was followed by a 20-week evaluation period.

Results: Of 229 patients screened, 164 were randomized (levetiracetam, n = 80; placebo, n = 84). Levetiracetam produced a greater mean reduction in GTC seizure frequency per week over the treatment period (56.5%) than placebo (28.2%; p = 0.004). The percentage of patients who had ≥50% reduction of GTC seizure frequency per week (responders) during the treatment period was 72.2% for levetiracetam and 45.2% for placebo (p < 0.001; OR 3.28; 95% CI 1.68 to 6.38). During the first 2-week treatment 64.6% of patients on levetiracetam and 45.2% on placebo (p = 0.018) were classified as responders. During the evaluation period the percent of patients free of GTC seizures (34.2% vs 10.7%; p < 0.001) and all seizure types (24.1% vs 8.3%; p = 0.009) was greater for levetiracetam than placebo. Levetiracetam was well tolerated with 1.3% of patients discontinuing therapy due to adverse events vs 4.8% on placebo.

Conclusion: Adjunctive levetiracetam is an effective and well-tolerated antiepileptic drug for treating generalized tonic-clonic seizures in patients with idiopathic generalized epilepsies.




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S. Noachtar, E. Andermann, P. Meyvisch, F. Andermann, W. B. Gough, J. Schiemann-Delgado, and For the N166 Levetiracetam Study Group
Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures
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Levetiracetam for Idiopathic Generalized Epilepsy
Journal Watch (General), November 6, 2007; 2007(1106): 2 - 2.
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