Population pharmacokinetics of eptinezumab in paediatric patients with migraine and dose selection for phase 3 paediatric migraine studies

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Johan Areberg, Monika Rosen, Annika Lindsten, Marianne Dragheim, Janka Ryding
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Abstract

This population pharmacokinetics (PopPK) analysis of eptinezumab used data from a paediatric study and a prior adult PopPK model to compare eptinezumab pharmacokinetics between adult and paediatric populations to determine dose recommendations for the phase 3 paediatric studies in migraine. The data consisted of 16 adolescents and 12 children with migraine, with corresponding demographics and 278 plasma concentrations in total. PopPK analysis was performed through nonlinear mixed effect modelling and with prior knowledge taken from a previous PopPK model in adults. A two-compartment model—adjusted for body weight impact on clearances and volumes of distributions and scaled to the power of 0.75 and 1.0, respectively—was found to adequately describe the paediatric pharmacokinetic data. The simulated population showed overlap in area under the plasma concentration–time curve and maximum plasma concentration between the paediatric and adult populations, with paediatric exposures within 10%–15% above adult levels on average. To provide comparable exposure to the approved adult doses, weight-based dosing adjustments are recommended for paediatric patients weighing ≤40 kg, while no adjustments are needed for patients weighing >40 kg. These results support the dosing strategy being used in the ongoing efficacy and safety studies with eptinezumab in children and adolescents with migraine.

Abstract Image

eptinezumab在儿科偏头痛患者中的群体药代动力学以及儿科偏头痛三期研究的剂量选择。
这项针对eptinezumab的群体药代动力学(PopPK)分析使用了一项儿科研究的数据和之前的成人PopPK模型,以比较成人和儿科群体的eptinezumab药代动力学,从而确定偏头痛儿科3期研究的剂量建议。数据包括16名青少年和12名儿童偏头痛患者的相应人口统计学特征和278个血浆浓度。PopPK分析是通过非线性混合效应模型进行的,并借鉴了之前成人PopPK模型的先验知识。根据体重对清除率和分布容积的影响进行调整,并分别按 0.75 和 1.0 的幂级数进行缩放的两室模型被认为能够充分描述儿科药代动力学数据。模拟人群显示,儿科和成人人群的血浆浓度-时间曲线下面积和最大血浆浓度存在重叠,儿科的暴露量平均比成人水平高出 10%-15%。为了提供与已批准的成人剂量相当的暴露量,建议对体重≤40 千克的儿科患者进行基于体重的剂量调整,而对体重大于 40 千克的患者则无需调整。这些结果支持目前正在进行的eptinezumab在儿童和青少年偏头痛患者中的疗效和安全性研究中所采用的剂量策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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