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药代动力学和药效学原理:新生儿临床试验优化设计的独特考量

Pharmacokinetic and pharmacodynamic principles: unique considerations for optimal design of neonatal clinical trials.

作者信息

Yeung Cindy Hoi Ting, Verstegen Ruud H J, Greenberg Rachel, Lewis Tamorah Rae

机构信息

Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children, Toronto, ON, Canada.

Department of Pediatrics, University of Toronto, Toronto, ON, Canada.

出版信息

Front Pediatr. 2024 Jan 12;11:1345969. doi: 10.3389/fped.2023.1345969. eCollection 2023.

Abstract

Core clinical pharmacology principles must be considered when designing and executing neonatal clinical trials. In this review, the authors discuss important aspects of drug dose selection, pharmacokinetics, pharmacogenetics and pharmacodynamics that stakeholders may consider when undertaking a neonatal or infant clinical trial.

摘要

在设计和开展新生儿临床试验时,必须考虑核心临床药理学原则。在本综述中,作者讨论了药物剂量选择、药代动力学、药物遗传学和药效学等重要方面,利益相关者在进行新生儿或婴儿临床试验时可能会考虑这些方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96cc/10811156/b510559331c8/fped-11-1345969-g001.jpg

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