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

机译:儿科药物开发中的新生儿药代动力学和药效学研究综述

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摘要

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.
机译: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年之间在新生儿或涉及新生儿中研究的43种药物。新生儿中批准了20种药物。对于10种药物,批准是基于新生儿的功效数据,再辅以四种药物的药代动力学数据。新生儿的批准是基于老年患者对六种药物的全面推断,而部分推断是对四种药物的批准基础。大多数药物的给药建议与老年患者不同,新生儿使用了基于体型的调整。试验失败与各种因素有关,包括剂量选择不当。对新生儿疾病的自然病史和病理生理学的进一步了解,以及临床相关生物标志物的鉴定和验证,可以促进新生儿药物的成功开发。

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