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通心络胶囊辅助治疗急性ST段抬高型心肌梗死(STEMI)患者的随机对照试验终点分析(节选)
通心络胶囊辅助治疗急性ST段抬高型心肌梗死(STEMI)患者的随机对照试验终点分析(节选)
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所属报告:
以岭药业(002603)-A股公司深度分析:中药创新领军者化生药+大健康协同拓增长-251121(41页).pdf
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行业数据
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行业数据
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行业数据
2023-09-11
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图表26麝香通心滴丸2017-2022销量(万盒;%)
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行业数据
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临床研究表明,通心络胶囊联合标准治疗可以显著改善 STEMI 患者的临床预后。急性 ST 段抬高型心肌梗死(STEMI)是全球范围内危及生命的主要疾病之一。在探究在指南指导疗法基础上加用通心络对 STEMI患者的临床疗效的一项随机临床试验中,主要终点显示,通心络组64名患者(3.4%)在 30天内发生主要不良心脑血管事件(MACCEs)事件,而安慰剂组有 99名患者(5.2%)在 30 天内发生同类事件;主要终点的单项指标中,30 天心血管死亡及再次心肌梗死在通心络组也显著更低。同时,与安慰剂组相比,通心络组的 1年 MACCEs发生率也更低,在 30天界值点后的发生率也显著降低,MACCEs的大多数单项指标发生率也显著降低,包括 1 年心血管死亡、再次心肌梗死和脑卒中。研究结果表明,STEMI 患者在指南推荐的治疗基础上使用通心络,可显著改善 30 天和 1年的临床结局。
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通心络胶囊辅助治疗急性ST段抬高型心肌梗死(STEMI)患者的随机对照试验终点分析(节选)
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