Department of Drug Metabolism and Pharmacokinetics, Sanofi-Genzyme, Waltham, MA 02451, United States.
Curr Drug Metab. 2020;21(6):403-426. doi: 10.2174/1389200221666200620210522.
In January 2020, the US FDA published two final guidelines, one entitled "In vitro Drug Interaction Studies - Cytochrome P450 Enzyme- and Transporter-Mediated Drug Interactions Guidance for Industry" and the other entitled "Clinical Drug Interaction Studies - Cytochrome P450 Enzyme- and Transporter-Mediated Drug Interactions Guidance for Industry". These were updated from the 2017 draft in vitro and clinical DDI guidance.
This study is aimed to provide an analysis of the updates along with a comparison of the DDI guidelines published by the European Medicines Agency (EMA) and Japanese Pharmaceuticals and Medical Devices Agency (PMDA) along with the current literature.
The updates were provided in the final FDA DDI guidelines and explained the rationale of those changes based on the understanding from research and literature. Furthermore, a comparison among the FDA, EMA, and PMDA DDI guidelines are presented in Tables 1, 2 and 3.
The new 2020 clinical DDI guidance from the FDA now has even higher harmonization with the guidance (or guidelines) from the EMA and PMDA. A comparison of DDI guidance from the FDA 2017, 2020, EMA, and PMDA on CYP and transporter based DDI, mathematical models, PBPK, and clinical evaluation of DDI is presented in this review.
2020 年 1 月,美国 FDA 发布了两份最终指南,一份题为“体外药物相互作用研究-细胞色素 P450 酶和转运体介导的药物相互作用行业指南”,另一份题为“临床药物相互作用研究-细胞色素 P450 酶和转运体介导的药物相互作用行业指南”。这些指南是对 2017 年体外和临床 DDI 指南草案的更新。
本研究旨在提供更新内容的分析,并与欧洲药品管理局(EMA)和日本药品和医疗器械管理局(PMDA)发布的 DDI 指南以及当前文献进行比较。
最终 FDA DDI 指南中提供了更新内容,并根据研究和文献的理解解释了这些变化的基本原理。此外,表 1、表 2 和表 3 还呈现了 FDA、EMA 和 PMDA DDI 指南之间的比较。
美国 FDA 新的 2020 年临床 DDI 指南现在与 EMA 和 PMDA 的指南更加协调一致。本文综述了 FDA 2017 年、2020 年、EMA 和 PMDA 基于 CYP 和转运体的 DDI、数学模型、PBPK 和 DDI 临床评估的 DDI 指南的比较。