TY - JOUR
T1 - Population Pharmacokinetic Modeling of Oxcarbazepine and Its Active Metabolite 10-Monohydroxy Derivative to Inform Dosing in Children with Obesity
AU - the Best Pharmaceuticals for Children Act—Pediatric Trials Network Steering Committee
AU - Sinha, Jaydeep
AU - Zimmerman, Kanecia
AU - Balevic, Stephen J.
AU - Hornik, Chi
AU - Muller, William J.
AU - Rathore, Mobeen
AU - Meyer, Marisa
AU - Finkelstein, Yaron
AU - Al-Uzri, Amira
AU - Lakhotia, Arpita
AU - Goldstein, Stuart
AU - Chen, Jia Yuh
AU - Anand, Ravinder
AU - Gonzalez, Daniel
AU - Massicotte, Christine
AU - Desmarasis, Diane
AU - Dumitrascu, Mariana
AU - Lague, Vincent
AU - Litalien, Catherine
AU - Autmizguine, Julie
AU - Dix, Megan
AU - DiDomenico, Domninic
AU - Hastenson, Gentle
AU - Ralston, Kimberly
AU - Steinbeiss, Matthew
AU - Deschenes, Jendar
AU - Malone, Kathryn
AU - Sierra, Yamila
AU - Rutebemberwa, Alleluiah
AU - Van, Kevin
AU - Goldenberg, Neil
AU - Mourani, Peter
AU - Lattimore, Susan
AU - Grzesek, Kimberly
AU - Craven, Sarah
AU - Clark, Kira
AU - Stubbs, Jennifer
AU - Kuchler, Andrea
AU - Farrar, Carrie
AU - Swanson, Connie
AU - Patubo, Kyle
AU - Murchison, Barbara
AU - Tuttle, Angie
AU - Leradi, Sara
AU - Lacaze, Thierry
AU - Zemek, Roger
AU - McMilan, Hugh
AU - Pohl, Daniela
AU - Mottes, Theresa
AU - Paul, Ian
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2026/2
Y1 - 2026/2
N2 - Background: Oxcarbazepine (OXZ) is an antiepileptic drug whose pharmacological effect is primarily mediated by its active metabolite, 10-monohydroxy derivative (MHD). OXZ is approved for use in adults and children older than 2 years with an age- and body weight-tiered dosing recommendation, but dosing guidance for children with obesity is lacking. Objective: This work aimed to assess the dosing requirements of OXZ in children with obesity to support label extension. Methods: Two multicenter studies (NCT01431326 and NCT02993861) were conducted in patients receiving standard-of-care OXZ therapy. Participants ≥ 2 years of age with a body mass index ≥ 95th percentile were classified as obese. Plasma concentrations were measured by a validated liquid chromatography tandem mass spectrometry (LC-MS/MS) assay. Nonlinear mixed effects modeling was performed using NONMEM 7.4 to characterize the population pharmacokinetics of OXZ and MHD simultaneously. Simulations were performed to compare MHD systemic exposure in children ≥ 2 years of age with and without obesity. Results: One hundred study participants with a median (range) age of 9 years (44 days–20.90 years) contributed 425 plasma concentrations of OXZ (n = 212) and MHD (n = 213). Fifty-two percent of the participants had obesity. A one-compartment joint parent–metabolite model with linear input–output and bi-directional transformation between OXZ and MHD best characterized the pharmacokinetics. Body size was the only covariate affecting pharmacokinetics, and a fat-free mass–based metric termed pharmacokinetic weight (PKWT) best characterized that effect allometrically. Simulation results revealed that the current dosing regimen of OXZ can produce comparable exposure of MHD in children ≥ 2 years of age with and without obesity. Conclusion: A model-informed analysis confirms that the current pediatric dosing regimen of OXZ applies to children in general, regardless of their obesity status.
AB - Background: Oxcarbazepine (OXZ) is an antiepileptic drug whose pharmacological effect is primarily mediated by its active metabolite, 10-monohydroxy derivative (MHD). OXZ is approved for use in adults and children older than 2 years with an age- and body weight-tiered dosing recommendation, but dosing guidance for children with obesity is lacking. Objective: This work aimed to assess the dosing requirements of OXZ in children with obesity to support label extension. Methods: Two multicenter studies (NCT01431326 and NCT02993861) were conducted in patients receiving standard-of-care OXZ therapy. Participants ≥ 2 years of age with a body mass index ≥ 95th percentile were classified as obese. Plasma concentrations were measured by a validated liquid chromatography tandem mass spectrometry (LC-MS/MS) assay. Nonlinear mixed effects modeling was performed using NONMEM 7.4 to characterize the population pharmacokinetics of OXZ and MHD simultaneously. Simulations were performed to compare MHD systemic exposure in children ≥ 2 years of age with and without obesity. Results: One hundred study participants with a median (range) age of 9 years (44 days–20.90 years) contributed 425 plasma concentrations of OXZ (n = 212) and MHD (n = 213). Fifty-two percent of the participants had obesity. A one-compartment joint parent–metabolite model with linear input–output and bi-directional transformation between OXZ and MHD best characterized the pharmacokinetics. Body size was the only covariate affecting pharmacokinetics, and a fat-free mass–based metric termed pharmacokinetic weight (PKWT) best characterized that effect allometrically. Simulation results revealed that the current dosing regimen of OXZ can produce comparable exposure of MHD in children ≥ 2 years of age with and without obesity. Conclusion: A model-informed analysis confirms that the current pediatric dosing regimen of OXZ applies to children in general, regardless of their obesity status.
UR - https://www.scopus.com/pages/publications/105022426455
UR - https://www.scopus.com/pages/publications/105022426455#tab=citedBy
U2 - 10.1007/s40262-025-01579-0
DO - 10.1007/s40262-025-01579-0
M3 - Article
C2 - 41247430
AN - SCOPUS:105022426455
SN - 0312-5963
VL - 65
SP - 329
EP - 344
JO - Clinical Pharmacokinetics
JF - Clinical Pharmacokinetics
IS - 2
ER -