首页> 美国卫生研究院文献>CPT: Pharmacometrics Systems Pharmacology >Exploratory Population PK Analysis of Dupilumab a Fully Human Monoclonal Antibody Against IL‐4Rα in Atopic Dermatitis Patients and Normal Volunteers
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Exploratory Population PK Analysis of Dupilumab a Fully Human Monoclonal Antibody Against IL‐4Rα in Atopic Dermatitis Patients and Normal Volunteers

机译:特应性皮炎患者和正常志愿者中抗IL-4Rα的全人类单克隆抗体Dupilumab的探索性人群PK分析

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摘要

An exploratory population pharmacokinetic model for functional dupilumab was developed. Data from healthy volunteers and patients with atopic dermatitis (AD) receiving intravenous or subcutaneous doses were integrated. The data included 197 participants (2,518 measurements of dupilumab in serum) from six phase I and II studies. The data were analyzed using stochastic approximation expectation‐maximization and importance sampling methods. The best structural model was a two‐compartment model with parallel linear and Michaelis–Menten elimination from the central compartment. Estimated parameters were: central volume 2.74 L, elimination rate 0.0459 d−1, central‐to‐peripheral rate 0.0652 d−1, peripheral‐to‐central rate 0.129 d−1, bioavailability 60.7%, maximal target‐mediated elimination rate 0.968 mg/L/d, and Michaelis–Menten constant 0.01 mg/L. Body weight was a significant covariate of the central volume. No gender effect was observed when controlling for weight. No differences between healthy volunteers and patients with AD were found. The model adequately described dupilumab pharmacokinetics for intravenous and subcutaneous routes of administration.
机译:开发了功能性dupilumab探索性人群药代动力学模型。来自健康志愿者和特应性皮炎(AD)的患者接受静脉内或皮下给药的数据已整合。数据包括来自I和II期六项研究的197名参与者(血清中dupilumab的2518次测量)。使用随机逼近期望最大化和重要性抽样方法对数据进行了分析。最好的结构模型是两室模型,在中央隔室中采用平行线性和Michaelis-Menten消除。估计参数为:中心体积2.74 L,消除速率0.0459 d -1 ,中心至外围速率0.0652 d -1 ,外围至中心速率0.129 d < sup> -1 ,生物利用度60.7%,目标介导的最大清除率0.968 mg / L / d,Michaelis-Menten常数0.01 mg / L。体重是中心体积的重要协变量。控制体重时未观察到性别效应。健康志愿者和AD患者之间没有发现差异。该模型充分描述了dupilumab静脉和皮下给药途径的药代动力学。

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