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儿科药物研发中的新生儿药代动力学和药效学研究综述。

A Survey of Neonatal Pharmacokinetic and Pharmacodynamic Studies in Pediatric Drug Development.

机构信息

Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Office of Pediatric Therapeutics, Commissioner's Office, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

出版信息

Clin Pharmacol Ther. 2015 Sep;98(3):328-35. doi: 10.1002/cpt.149.

Abstract

Conducting clinical trials in neonates is challenging, and knowledge gaps in neonatal clinical pharmacology exist. We surveyed the US Food and Drug Administration databases and identified 43 drugs studied in neonates or referring to neonates between 1998 and 2014. Twenty drugs were approved in neonates. For 10 drugs, approval was based on efficacy data in neonates, supplemented by pharmacokinetic data for four drugs. Approval for neonates was based on full extrapolation from older patients for six drugs, and partial extrapolation was the basis of approval for four drugs. Dosing recommendations differed from older patients for most drugs, and used body-size based adjustment in neonates. Trial failures were associated with various factors including inappropriate dose selection. Successful drug development in neonates could be facilitated by an improved understanding of the natural history and pathophysiology of neonatal diseases and identification and validation of clinically relevant biomarkers.

摘要

在新生儿中进行临床试验具有挑战性,并且新生儿临床药理学方面存在知识空白。我们调查了美国食品和药物管理局的数据库,确定了 1998 年至 2014 年期间在新生儿中或针对新生儿进行研究的 43 种药物。有 20 种药物在新生儿中获得批准。对于 10 种药物,批准是基于新生儿中的疗效数据,并为其中 4 种药物补充了药代动力学数据。有 6 种药物的批准是基于从年龄较大的患者中完全外推,4 种药物的批准是基于部分外推。对于大多数药物,新生儿的剂量建议与年龄较大的患者不同,并且使用基于体大小的调整。试验失败与各种因素有关,包括不合适的剂量选择。通过更好地了解新生儿疾病的自然史和病理生理学,并确定和验证临床相关的生物标志物,可以促进新生儿药物的成功开发。

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