医学
临床终点
安慰剂
肥厚性心肌病
内科学
临床试验
代理终结点
心脏病学
人口
不利影响
心肌病
心脏磁共振成像
冠状动脉疾病
心力衰竭
磁共振成像
病理
替代医学
环境卫生
放射科
作者
Zhuang Tian,Fang Wang,Wei Jin,Qing Zhang,Jingmin Zhou,Ping Yang,Geng Wang,Peiwen Hsu,Jing Sun,Shuyang Zhang,Yaling Han
出处
期刊:BMJ Open
[BMJ]
日期:2023-06-01
卷期号:13 (6): e071473-e071473
被引量:8
标识
DOI:10.1136/bmjopen-2022-071473
摘要
Hypertrophic cardiomyopathy (HCM) is a primary myocardial disease commonly caused by pathogenic genetic variants encoding sarcomere proteins. Mavacamten, a first-in-class allosteric inhibitor of cardiac-specific myosin, has demonstrated efficacy and safety in international clinical trials of patients with symptomatic obstructive HCM (oHCM) but clinical evidence for mavacamten in the Chinese population is lacking.
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