Kovalenko P, DiCioccio A T, Davis J D, Li M, Ardeleanu M, Graham Nmh, Soltys R
Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
Sanofi, Bridgewater, New Jersey, USA.
CPT Pharmacometrics Syst Pharmacol. 2016 Nov;5(11):617-624. doi: 10.1002/psp4.12136. Epub 2016 Oct 25.
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 , central-to-peripheral rate 0.0652 d , peripheral-to-central rate 0.129 d , 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.
建立了功能性度普利尤单抗的探索性群体药代动力学模型。整合了来自健康志愿者和接受静脉或皮下给药剂量的特应性皮炎(AD)患者的数据。这些数据包括来自六项I期和II期研究的197名参与者(血清中度普利尤单抗的2518次测量)。使用随机近似期望最大化和重要性抽样方法对数据进行分析。最佳结构模型是一个二室模型,从中央室进行平行线性消除和米氏消除。估计参数为:中央室容积2.74L,消除率0.0459d,中央室到外周室速率0.0652d,外周室到中央室速率0.129d,生物利用度60.7%,最大靶介导消除率0.968mg/L/d,米氏常数0.01mg/L。体重是中央室容积的显著协变量。在控制体重时未观察到性别效应。未发现健康志愿者和AD患者之间存在差异。该模型充分描述了度普利尤单抗静脉和皮下给药途径的药代动力学。