Pharmacokinetic Study of Levetiracetam in Children
Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open‐label, single‐dose study. Methods: Twenty‐four children (15 boys, nine girls), 6 to 12 years old, received a sin...
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Published in | Epilepsia (Copenhagen) Vol. 42; no. 12; pp. 1574 - 1579 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston, MA, USA
Blackwell Science Inc
01.12.2001
Blackwell |
Subjects | |
Online Access | Get full text |
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Abstract | Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open‐label, single‐dose study.
Methods: Twenty‐four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24‐h pharmacokinetic evaluation.
Results: In children, the half‐lives of levetiracetam and its metabolite ucb L057 were 6.0 ± 1.1 and 8.1 ± 2.7 hours, respectively. The Cmax and area under the curve (AUC) of levetiracetam equated for a 1‐mg/kg dose were lower in children (Cmax, norm = 1.33 ± 0.35 μg/ml; AUCnorm = 12.4 ± 3.5 μg/h/ml) than in adults (Cmax, norm = 1.38 ± 0.05 μg/ml; AUCnorm = 11.48 ± 0.63 μg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 ± 0.36 ml/min/kg) was ∼30–40% higher in children than in adults. Levetiracetam was generally well tolerated.
Conclusions: On the basis of these data, a daily maintenance dose equivalent to 130–140% of the usual daily adult maintenance dosage (1,000–3,000 mg/day) in two divided doses, on a weight‐normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day. |
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AbstractList | The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open-label, single-dose study.
Twenty-four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24-h pharmacokinetic evaluation.
In children, the half-lives of levetiracetam and its metabolite ucb L057 were 6.0 +/- 1.1 and 8.1 +/-2.7 hours, respectively. The Cmax and area under the curve (AUC) of levetiracetam equated for a 1-mg/kg dose were lower in children (Cmax, norm=1.33 plus minus 0.35 microg/ml; AUCnorm=12.4 +/- 3.5 microg/h/ml) than in adults (Cmax, norm=1.38 +/- 0.05 microg/ml; AUCnorm=11.48 +/- 0.63 microg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 +/- 0.36 ml/min/kg) was approximately 30-40% higher in children than in adults. Levetiracetam was generally well tolerated.
On the basis of these data, a daily maintenance dose equivalent to 130-140% of the usual daily adult maintenance dosage (1,000-3,000 mg/day) in two divided doses, on a weight-normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day. The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open-label, single-dose study.PURPOSEThe pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open-label, single-dose study.Twenty-four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24-h pharmacokinetic evaluation.METHODSTwenty-four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24-h pharmacokinetic evaluation.In children, the half-lives of levetiracetam and its metabolite ucb L057 were 6.0 +/- 1.1 and 8.1 +/-2.7 hours, respectively. The Cmax and area under the curve (AUC) of levetiracetam equated for a 1-mg/kg dose were lower in children (Cmax, norm=1.33 plus minus 0.35 microg/ml; AUCnorm=12.4 +/- 3.5 microg/h/ml) than in adults (Cmax, norm=1.38 +/- 0.05 microg/ml; AUCnorm=11.48 +/- 0.63 microg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 +/- 0.36 ml/min/kg) was approximately 30-40% higher in children than in adults. Levetiracetam was generally well tolerated.RESULTSIn children, the half-lives of levetiracetam and its metabolite ucb L057 were 6.0 +/- 1.1 and 8.1 +/-2.7 hours, respectively. The Cmax and area under the curve (AUC) of levetiracetam equated for a 1-mg/kg dose were lower in children (Cmax, norm=1.33 plus minus 0.35 microg/ml; AUCnorm=12.4 +/- 3.5 microg/h/ml) than in adults (Cmax, norm=1.38 +/- 0.05 microg/ml; AUCnorm=11.48 +/- 0.63 microg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 +/- 0.36 ml/min/kg) was approximately 30-40% higher in children than in adults. Levetiracetam was generally well tolerated.On the basis of these data, a daily maintenance dose equivalent to 130-140% of the usual daily adult maintenance dosage (1,000-3,000 mg/day) in two divided doses, on a weight-normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day.CONCLUSIONSOn the basis of these data, a daily maintenance dose equivalent to 130-140% of the usual daily adult maintenance dosage (1,000-3,000 mg/day) in two divided doses, on a weight-normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day. Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open‐label, single‐dose study. Methods: Twenty‐four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24‐h pharmacokinetic evaluation. Results: In children, the half‐lives of levetiracetam and its metabolite ucb L057 were 6.0 ± 1.1 and 8.1 ± 2.7 hours, respectively. The Cmax and area under the curve (AUC) of levetiracetam equated for a 1‐mg/kg dose were lower in children (Cmax, norm = 1.33 ± 0.35 μg/ml; AUCnorm = 12.4 ± 3.5 μg/h/ml) than in adults (Cmax, norm = 1.38 ± 0.05 μg/ml; AUCnorm = 11.48 ± 0.63 μg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 ± 0.36 ml/min/kg) was ∼30–40% higher in children than in adults. Levetiracetam was generally well tolerated. Conclusions: On the basis of these data, a daily maintenance dose equivalent to 130–140% of the usual daily adult maintenance dosage (1,000–3,000 mg/day) in two divided doses, on a weight‐normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day. Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in a multicenter, open‐label, single‐dose study. Methods: Twenty‐four children (15 boys, nine girls), 6 to 12 years old, received a single dose of levetiracetam (20 mg/kg) as an adjunct to their stable regimen of a single concomitant AED, followed by a 24‐h pharmacokinetic evaluation. Results: In children, the half‐lives of levetiracetam and its metabolite ucb L057 were 6.0 ± 1.1 and 8.1 ± 2.7 hours, respectively. The C max and area under the curve (AUC) of levetiracetam equated for a 1‐mg/kg dose were lower in children (C max, norm = 1.33 ± 0.35 μg/ml; AUC norm = 12.4 ± 3.5 μg/h/ml) than in adults (C max, norm = 1.38 ± 0.05 μg/ml; AUC norm = 11.48 ± 0.63 μg/h/ml), whereas the renal clearance was higher. The apparent body clearance (1.43 ± 0.36 ml/min/kg) was ∼30–40% higher in children than in adults. Levetiracetam was generally well tolerated. Conclusions: On the basis of these data, a daily maintenance dose equivalent to 130–140% of the usual daily adult maintenance dosage (1,000–3,000 mg/day) in two divided doses, on a weight‐normalized level (mg/kg/day) is initially recommended. Clinical efficacy trials in children are ongoing with dosages of 20 to 60 mg/kg/day. |
Author | COUPEZ Rene M. PELLOCK John M. FOUNTAIN Nathan B. GLAUSER Tracy A. BEBIN E. Martina RITTER Frank J. SHIELDS W. Donald |
Author_xml | – sequence: 1 givenname: John M. surname: Pellock fullname: Pellock, John M. – sequence: 2 givenname: Tracy A. surname: Glauser fullname: Glauser, Tracy A. – sequence: 3 givenname: E. Martina surname: Bebin fullname: Bebin, E. Martina – sequence: 4 givenname: Nathan B. surname: Fountain fullname: Fountain, Nathan B. – sequence: 5 givenname: Frank J. surname: Ritter fullname: Ritter, Frank J. – sequence: 6 givenname: René M. surname: Coupez fullname: Coupez, René M. – sequence: 7 givenname: W. Donald surname: Shields fullname: Shields, W. Donald |
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Keywords | Human Nervous system diseases Metabolite Epilepsy Multicenter study Anticonvulsant Clearance Metabolism Cerebral disorder Chemotherapy Treatment Partial Central nervous system disease Pharmacokinetics Child Levetiracetam |
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References_xml | – volume: 85 start-page: 77 year: 2000 end-page: 85 article-title: Pharmacokinetic profile of levetiracetam: toward ideal characteristics. publication-title: Pharmacol Ther – volume: 104 start-page: 1106 year: 1999 end-page: 16 article-title: Managing pediatric epilepsy syndromes with new antiepileptic drugs. publication-title: Pediatrics – volume: 41 start-page: 1179 year: 2000 end-page: 86 article-title: Multicenter double‐blind, randomized, placebo‐controlled trial of levetiracetam as add‐on therapy in patients with refractory partial seizures. publication-title: Epilepsia – volume: 9 start-page: 80 year: 2000 end-page: 7 article-title: A multicentre, double‐blind, randomized, parallel group study to evaluate the tolerability and efficacy of two oral doses of levetiracetam, 2000 mg daily and 4000 mg daily, without titration in patients with refractory epilepsy. publication-title: Seizure – volume: 37 start-page: 1160 year: 1997 end-page: 7 article-title: Population‐based investigation of valproic acid relative clearance using nonlinear mixed effects modeling: influence of drug‐drug interaction and patient characteristics. publication-title: J Clin Pharmacol – volume: 19 start-page: 411 year: 1995 end-page: 9 article-title: Cognitive effects of a new pyrrolidine derivative (levetiracetam) in patients with epilepsy. publication-title: Prog Neuropsychopharmacol Biol Psychiatry – volume: 55 start-page: 236 year: 2000 end-page: 42 article-title: Levetiracetam for partial seizures: results of a double‐blind, randomized clinical trial. publication-title: Neurology – volume: 41 start-page: 1276 year: 2000 end-page: 83 article-title: Efficacy and tolerability of levetiracetam 3000 mg/day in patients with refractory partial seizures: a multicenter, double‐blind, responder‐selected study evaluating monotherapy. publication-title: Epilepsia – volume: 20 start-page: 339 year: 1999 end-page: 44 article-title: A study of topiramate pharmacokinetics and tolerability in children with epilepsy. publication-title: Pediatr Neurol – volume: 48 start-page: 1032 year: 1997 end-page: 7 article-title: A single‐dose study to define tiagabine pharmacokinetics in pediatric patients with complex partial seizures. publication-title: Neurology – volume: 284 start-page: 474 year: 1998 end-page: 9 article-title: Antiepileptic effects of the novel anticonvulsant levetiracetam (ucb L059) in the kindling model of temporal lobe epilepsy. publication-title: J Pharmacol Exp Ther – volume: 81 start-page: 309 year: 1992 end-page: 12 article-title: Analytical methods validation: bioavailability, bioequivalence and pharmacokinetic studies. publication-title: J Pharm Sci – ident: e_1_2_6_2_2 doi: 10.1212/WNL.55.2.236 – ident: e_1_2_6_6_2 doi: 10.1016/S0163-7258(99)00052-2 – ident: e_1_2_6_7_2 doi: 10.1016/0278-5846(95)00022-N – ident: e_1_2_6_12_2 doi: 10.1002/j.1552-4604.1997.tb04301.x – ident: e_1_2_6_3_2 doi: 10.1111/j.1528-1157.2000.tb00323.x – ident: e_1_2_6_10_2 doi: 10.1002/jps.2600810324 – ident: e_1_2_6_4_2 doi: 10.1111/j.1528-1157.2000.tb04605.x – volume: 284 start-page: 474 year: 1998 ident: e_1_2_6_8_2 article-title: Antiepileptic effects of the novel anticonvulsant levetiracetam (ucb L059) in the kindling model of temporal lobe epilepsy. publication-title: J Pharmacol Exp Ther – ident: e_1_2_6_5_2 doi: 10.1053/seiz.2000.0380 – ident: e_1_2_6_13_2 doi: 10.1016/S0887-8994(99)00011-9 – ident: e_1_2_6_11_2 doi: 10.1212/WNL.48.4.1032 – ident: e_1_2_6_9_2 doi: 10.1542/peds.104.5.1106 |
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Snippet | Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial... Purpose: The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial... The pharmacokinetics of the novel antiepileptic drug (AED) levetiracetam and its major metabolite, ucb L057, were studied in children with partial seizures in... |
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SubjectTerms | Adult Age Factors Anticonvulsants - pharmacokinetics Anticonvulsants - therapeutic use Anticonvulsants. Antiepileptics. Antiparkinson agents Biological and medical sciences Child Creatine - metabolism Epilepsy Epilepsy - drug therapy Epilepsy - metabolism Female Humans Keppra Levetiracetam Male Medical sciences Metabolic Clearance Rate Middle Aged Neuropharmacology Pediatric Pharmacokinetics Pharmacology. Drug treatments Piracetam - analogs & derivatives Piracetam - pharmacokinetics Piracetam - therapeutic use ucb L057 |
Title | Pharmacokinetic Study of Levetiracetam in Children |
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