Massachusetts General Hospital, Boston, MA, USA.
Sanofi, Bridgewater, NJ, USA.
Mol Genet Metab. 2020 Sep-Oct;131(1-2):211-218. doi: 10.1016/j.ymgme.2020.09.003. Epub 2020 Sep 16.
Eliglustat is a first-line oral treatment for adults with Gaucher disease type 1 who have cytochrome P450 (CYP) 2D6 extensive, intermediate, or poor metabolizer phenotypes. Per International Conference on Harmonisation (ICH) E14 guidance, a Phase 1 thorough electrocardiographic (ECG) study was done during drug development to assess eliglustat's effects on cardiac repolarization by measuring ECG intervals in healthy adult subjects. Using data from the thorough ECG study, we performed pharmacokinetic/pharmacodynamic-ECG modeling to establish the relationship between eliglustat concentrations and their effects on ECG intervals. We then used that concentration-response relationship to predict the effects of eliglustat on each ECG interval for each CYP2D6 metabolizer phenotype (the main determinant of eliglustat exposure) and in different drug-drug interaction scenarios. These predictions, together with other exposure-related factors, contributed to the CYP2D6 phenotype-based dosing recommendations for eliglustat, including dose adjustments and contraindications when co-administered with drugs metabolized by the CYP2D6 and CYP3A pathways.
依鲁替尼是治疗 1 型戈谢病的一线口服药物,适用于细胞色素 P450(CYP)2D6 广泛、中间或弱代谢表型的成年患者。根据国际协调会议(ICH)E14 指南,在药物开发过程中进行了一项全面的 1 期心电图(ECG)研究,以通过测量健康成年受试者的 ECG 间期来评估依鲁替尼对心脏复极的影响。我们使用全面的 ECG 研究数据,进行了药代动力学/药效学-ECG 建模,以建立依鲁替尼浓度与其对 ECG 间期影响之间的关系。然后,我们使用该浓度-反应关系来预测依鲁替尼对每个 CYP2D6 代谢表型(依鲁替尼暴露的主要决定因素)的每个 ECG 间期的影响,以及在不同的药物相互作用情况下。这些预测结果,以及其他与暴露相关的因素,有助于为依鲁替尼建立基于 CYP2D6 表型的给药建议,包括与 CYP2D6 和 CYP3A 途径代谢的药物联合使用时的剂量调整和禁忌证。