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临床试验中的青少年。

Adolescents in clinical trials.

作者信息

Kapogiannis B G, Mattison D R

机构信息

Pediatric, Adolescent, and Maternal AIDS Branch, Center for Research for Mothers and Children, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, MD, USA.

出版信息

Clin Pharmacol Ther. 2008 Dec;84(6):655-9. doi: 10.1038/clpt.2008.191.

Abstract

Drug development is a lengthy, costly, and complex process, with clinical trials essential for characterizing dosing, safety, and efficacy in treated populations. After regulatory approval, aggressive marketing ensures that most drugs are used by a broad spectrum of ages, genders, races, and ethnic groups. Unfortunately, not all groups are adequately represented in clinical trials; adolescents are commonly overlooked. This commentary explores how adolescents are considered during drug development, with a special focus on the influence of inherent psychosocial, biological, ethical, and regulatory issues in their recruitment and participation in clinical studies leading to drug licensing.

摘要

药物研发是一个漫长、昂贵且复杂的过程,临床试验对于确定治疗人群的给药剂量、安全性和疗效至关重要。在获得监管批准后,积极的市场营销确保大多数药物被广泛的年龄、性别、种族和族裔群体使用。不幸的是,并非所有群体在临床试验中都有充分的代表性;青少年通常被忽视。本评论探讨了在药物研发过程中如何考虑青少年,特别关注他们在招募和参与导致药物获批的临床研究中所面临的内在心理社会、生物学、伦理和监管问题的影响。

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