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成人药物研发与测试中的年龄和性别

Age and sex in drug development and testing for adults.

作者信息

Tannenbaum Cara, Day Danielle

机构信息

Institute of Gender and Health, Canadian Institutes of Health Research, Canada; Medicine and Pharmacy, Université de Montreal, Centre de recherche, Institut universitaire de gériatrie de Montréal (CRIUGM), 4565 Chemin Queen-Mary, Montréal, Québec H3W 1W5, Canada.

Fractyl Laboratories, 17 Hartwell Ave, Lexington, MA 02421, USA.

出版信息

Pharmacol Res. 2017 Jul;121:83-93. doi: 10.1016/j.phrs.2017.04.027. Epub 2017 Apr 26.

Abstract

Individualization of drug therapy requires that the right drug be administered at the correct dose to patients who are likely to achieve the highest benefit and lowest risk. Female sex and age comprise two important risk factors for altered drug exposure and response. This review summarizes the current state of science for considering age and sex-related factors along the drug development pipeline, from cell culture and animal research through all phases of clinical trials in humans. A set of recommendations is provided to improve standards for integrating age and sex into the study design, analysis, and reporting of pre-clinical and clinical assessment of new molecular entities and biologics in adults.

摘要

药物治疗的个体化要求将正确的药物以正确的剂量给予那些可能获得最大益处且风险最低的患者。女性性别和年龄是药物暴露和反应改变的两个重要风险因素。本综述总结了在药物研发过程中,从细胞培养和动物研究到人类临床试验的各个阶段,考虑年龄和性别相关因素的科学现状。文中提供了一系列建议,以提高在成人新分子实体和生物制品的临床前和临床评估的研究设计、分析及报告中纳入年龄和性别的标准。

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