Department of Clinical Pharmacology, Modeling and Simulation, Amgen Inc., One Amgen Center Drive, Thousand Oaks, CA, 91320, USA.
SGS Exprimo NV, Mechlin, Belgium.
Clin Pharmacokinet. 2018 Jan;57(1):71-85. doi: 10.1007/s40262-017-0550-4.
Etelcalcetide is a novel calcimimetic that binds and activates calcium-sensing receptors (CaSRs) for the treatment of secondary hyperparathyroidism (SHPT).
To assess titrated dosing regimens, population pharmacokinetic (PK) and PK/pharmacodynamic (PKPD) modeling of etelcalcetide was performed using NONMEM 7.2. In this analysis, plasma etelcalcetide, serum parathyroid hormone (PTH) and calcium (Ca) concentration-time data were collected from five phase I, II, and III clinical trials following single or multiple intravenous doses of etelcalcetide ranging from 2.5 to 60 mg. A semi-mechanistic model was used to describe the relationship between etelcalcetide, PTH, and Ca. This model included the role of PTH in Ca regulation, the feedback of Ca onto PTH production via the CaSR, and the activity of etelcalcetide plasma levels in increasing the sensitivity of the CaSR to Ca via the cooperative binding model. The impact of relevant covariates was evaluated by stepwise forward/backward selection. Model evaluation was based on standard goodness-of-fit plots and prediction-corrected visual predictive checks (pcVPCs). Simulation was conducted to evaluate titrated dosing regimens.
The time courses of etelcalcetide, PTH, and Ca were well-described by the model. The clearance and central volume of distribution (Vc) of etelcalcetide were 0.472 L/h and 49.9 L, respectively, while estimates of the turnover half-lives of PTH and Ca were 0.36 and 23 h, respectively. The extent of interindividual variability in model parameters was low to moderate (6-67%), and no covariates were identified as significant predictors of PK and PD variability. pcVPCs confirmed the predictive ability of the model.
The current analysis confirms the putative mechanism of action of etelcalcetide as an allosteric activator of CaSR. Simulations showed that dose titration of etelcalcetide, rather than fixed dose, is needed to effectively decrease the PTH level in patient populations.
依特卡塞特是一种新型的钙敏感受体激动剂,用于治疗继发性甲状旁腺功能亢进症(SHPT)。
为评估滴定剂量方案,采用 NONMEM 7.2 对依特卡塞特的群体药代动力学(PK)和 PK/药效动力学(PKPD)进行建模。在这项分析中,从五项 I、II 和 III 期临床试验中收集了单次或多次静脉注射依特卡塞特 2.5 至 60mg 后的血浆依特卡塞特、血清甲状旁腺激素(PTH)和钙(Ca)浓度-时间数据。采用半机理模型描述依特卡塞特、PTH 和 Ca 之间的关系。该模型包括 PTH 在 Ca 调节中的作用、Ca 通过钙敏感受体对 PTH 产生的反馈,以及依特卡塞特血浆水平通过协同结合模型增加 CaSR 对 Ca 的敏感性的作用。通过逐步正向/反向选择评估了相关协变量的影响。模型评估基于标准的拟合优度图和预测校正可视化预测检查(pcVPC)。通过模拟评估滴定剂量方案。
该模型很好地描述了依特卡塞特、PTH 和 Ca 的时间过程。依特卡塞特的清除率和中央分布容积(Vc)分别为 0.472L/h 和 49.9L,而 PTH 和 Ca 的半衰期估计值分别为 0.36 和 23h。模型参数的个体间变异性程度较低至中等(6-67%),未发现有任何协变量可显著预测 PK 和 PD 的变异性。pcVPC 证实了该模型的预测能力。
本分析证实了依特卡塞特作为 CaSR 变构激活剂的作用机制。模拟结果表明,需要对依特卡塞特进行剂量滴定,而不是固定剂量,以有效降低患者群体中的 PTH 水平。