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儿科药代动力学和剂量预测:第 10 届青少年毒性研讨会卫星会议报告。

Pediatric Pharmacokinetics and Dose Predictions: A Report of a Satellite Meeting to the 10th Juvenile Toxicity Symposium.

机构信息

Intensive Care and Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.

Roche Pharma and Early Development (pRED), Roche Innovation Center Basel, Basel, Switzerland.

出版信息

Clin Transl Sci. 2021 Jan;14(1):29-35. doi: 10.1111/cts.12843. Epub 2020 Aug 3.

Abstract

On April 24, 2019, a symposium on Pediatric Pharmacokinetics and Dose Predictions was held as a satellite meeting to the 10th Juvenile Toxicity Symposium. This symposium brought together scientists from academia, industry, and clinical research organizations with the aim to update each other on the current knowledge on pediatric drug development. Through more knowledge on specific ontogeny profiles of drug metabolism and transporter proteins, integrated into physiologically-based pharmacokinetic (PBPK) models, we have gained a more integrated understanding of age-related differences in pharmacokinetics (PKs), Relevant examples were presented during the meeting. PBPK may be considered the gold standard for pediatric PK prediction, but still it is important to know that simpler methods, such as allometry, allometry combined with maturation function, functions based on the elimination pathway, or linear models, also perform well, depending on the age range or the mechanisms involved. Knowledge from different methods and information sources should be combined (e.g., microdosing can reveal early read-out of age-related differences in exposure), and such results can be a value to verify models. To further establish best practices for dose setting in pediatrics, more in vitro and in vivo research is needed on aspects such as age-related changes in the exposure-response relationship and the impact of disease on PK. New information coupled with the refining of model-based drug development approaches will allow faster targeting of intended age groups and allow more efficient design of pediatric clinical trials.

摘要

2019 年 4 月 24 日,在第十届青少年毒性研讨会的卫星会议上举办了儿科药代动力学和剂量预测研讨会。本次研讨会汇集了来自学术界、工业界和临床研究组织的科学家,旨在更新儿科药物开发方面的最新知识。通过更深入地了解药物代谢和转运蛋白的特定个体发育特征,并将其整合到基于生理学的药代动力学 (PBPK) 模型中,我们对与年龄相关的药代动力学 (PK) 差异有了更全面的认识。会上介绍了相关实例。PBPK 可被视为儿科 PK 预测的黄金标准,但仍需要知道,更简单的方法,如比例法、比例法结合成熟函数、基于消除途径的函数或线性模型,也能根据年龄范围或涉及的机制,取得良好的效果。应结合来自不同方法和信息源的知识(例如,微剂量可以揭示与暴露相关的与年龄相关差异的早期读数),并且此类结果可以作为验证模型的价值。为了进一步为儿科剂量设定建立最佳实践,需要在与暴露-反应关系的年龄相关性变化以及疾病对 PK 的影响等方面开展更多的体外和体内研究。新信息加上对基于模型的药物开发方法的改进,将使目标年龄组更快地定位,并使儿科临床试验的设计更有效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8434/7877839/8976d7e5d89d/CTS-14-29-g001.jpg

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