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心力衰竭药物研发的终点:历史与未来。

Endpoints in Heart Failure Drug Development: History and Future.

机构信息

Duke University and Duke Clinical Research Institute, Durham, North Carolina; U.S. Food and Drug Administration, Silver Spring, Maryland.

U.S. Food and Drug Administration, Silver Spring, Maryland.

出版信息

JACC Heart Fail. 2020 Jun;8(6):429-440. doi: 10.1016/j.jchf.2019.12.011. Epub 2020 Apr 8.

Abstract

Heart failure (HF) patients experience a high burden of symptoms and functional limitations, and morbidity and mortality remain high despite successful therapies. The majority of HF drugs in the United States are approved for reducing hospitalization and mortality, while only a few have indications for improving quality of life, physical function, or symptoms. Patient-reported outcomes that directly measure patient's perception of health status (symptoms, physical function, or quality of life) are potentially approvable endpoints in drug development. This paper summarizes the history of endpoints used for HF drug approvals in the United States and reviews endpoints that measure symptoms, physical function, or quality of life in HF patients.

摘要

心力衰竭(HF)患者承受着高症状负担和功能限制的困扰,尽管治疗取得了成功,但发病率和死亡率仍然居高不下。美国大多数 HF 药物的批准用途是减少住院和死亡,而只有少数药物有改善生活质量、身体功能或症状的适应证。直接衡量患者对健康状况(症状、身体功能或生活质量)感知的患者报告结局,可能是药物开发中可批准的终点。本文总结了美国 HF 药物批准使用的终点的历史,并回顾了用于 HF 患者的测量症状、身体功能或生活质量的终点。

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