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2017 ACC/AAP/AHA Health Policy Statement on Opportunities and Challenges in Pediatric Drug Development: Learning From Sildenfil

机译:2017年ACC / AAP / AHA卫生政策声明中关于儿科药物开发的机遇与挑战:向Sildenfil学习

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摘要

The STARTS-1 and -2 trials (Sildenafil in Treatment-Naive Children, Aged 1 to 17 Years, With Pulmonary Arterial Hypertension) and subsequent 2012 U.S. Food and Drug Administration (FDA) product labeling for sildenafil use in pediatric patients with pulmonary hypertension highlight many of the challenges to the development and approval of medications for children. This experience served as the impetus for direct collaboration between FDA representatives and the Joint Council on Congenital Heart Disease (JCCHD) (representing the pediatric cardiology leadership of the American College of Cardiology, the American Heart Association, and the American Academy of Pediatrics) to improve communication and realign missions with regard to pediatric drug trials. These discussions led to the joint FDA/JCCHD development of this statement, which describes the current environment and identifies possible future directions for reducing barriers to pediatric drug trials.
机译:STARTS-1和-2试验(未接受过治疗的儿童使用西地那非,年龄1至17岁,患有肺动脉高压)以及随后的2012年美国食品药品监督管理局(FDA)产品标签,表明西地那非用于小儿肺动脉高压患者儿童药物开发和批准面临的许多挑战。这项经验为FDA代表与先天性心脏病联合委员会(JCCHD)(代表美国心脏病学会,美国心脏协会和美国儿科学会的儿科心脏病学领导者)之间直接合作提供了动力就儿科药物试验进行沟通并调整任务。这些讨论促成了FDA / JCCHD联合声明的制定,该声明描述了当前环境并确定了减少儿科药物试验障碍的未来可能方向。

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