Clinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Gothenburg, Sweden.
Clinical Pharmacology & Quantitative Pharmacology, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Gaithersburg, Maryland, USA.
J Clin Pharmacol. 2022 Oct;62(10):1227-1235. doi: 10.1002/jcph.2062. Epub 2022 May 2.
Dapagliflozin improves glycemic control in patients with type 2 diabetes mellitus (T2DM) and is approved in Japanese patients with type 1 diabetes mellitus (T1DM) with inadequate glycemic control. The objectives of this work were to characterize the dapagliflozin pharmacokinetics (PK) in patients with T1DM, assess the influence of covariates on dapagliflozin PK, and compare dapagliflozin systemic exposure between patients with T1DM and T2DM. Population PK analysis was performed using a nonlinear mixed-effect modeling approach. The analysis included 5793 dapagliflozin plasma concentrations from 1150 adult patients with T1DM (global population), who were on routine insulin therapy, collected from 1 phase 2 (NCT01498185) and 2 phase 3 (DEPICT-1, NCT02268214; DEPICT-2, NCT02460978) studies. Covariate effects were investigated using stepwise covariate modeling. Model-derived area under the concentration-time curve (AUC) in patients with T1DM was compared to AUC in patients with T2DM (using data from historical dapagliflozin studies). The final 2-compartmental model adequately described the dapagliflozin concentrations in patients with T1DM. The estimated apparent clearance was 20.5 L/h. Renal function (measured as estimated glomerular filtration rate), sex, and body weight were identified as covariates, where patients with better renal function, male patients, and heavier patients had lower dapagliflozin systemic exposure. Among the covariates studied, none of the covariates affected dapagliflozin systemic exposure >1.4-fold compared to a reference individual and were therefore deemed to be not clinically relevant. Dapagliflozin systemic exposure was comparable between patients with T1DM and T2DM.
达格列净可改善 2 型糖尿病(T2DM)患者的血糖控制,在血糖控制不佳的 1 型糖尿病(T1DM)日本患者中获得批准。本研究旨在描述 T1DM 患者的达格列净药代动力学(PK)特征,评估协变量对达格列净 PK 的影响,并比较 T1DM 和 T2DM 患者之间的达格列净系统暴露。采用非线性混合效应模型方法进行群体 PK 分析。该分析纳入了 1150 名接受常规胰岛素治疗的 T1DM 成年患者(总体人群)的 5793 个达格列净血浆浓度,来自 2 项 2 期(NCT01498185)和 2 项 3 期(DEPICT-1,NCT02268214;DEPICT-2,NCT02460978)研究。采用逐步协变量建模法研究协变量效应。使用来自达格列净历史研究的数据,比较了 T1DM 患者的模型推导的 AUC 与 T2DM 患者的 AUC。最终的 2 室模型能够充分描述 T1DM 患者的达格列净浓度。估计的表观清除率为 20.5 L/h。肾功能(以估算肾小球滤过率衡量)、性别和体重被确定为协变量,肾功能较好、男性和体重较重的患者达格列净系统暴露较低。在研究的协变量中,与参考个体相比,没有任何协变量使达格列净系统暴露增加超过 1.4 倍,因此被认为不具有临床意义。T1DM 和 T2DM 患者的达格列净系统暴露相当。