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临床试验/CTIS2023-508292-37-00
CTIS2023-508292-37-00进行中(未招募)1 期

A randomized double-blind, placebo-controlled, multicenter trial assessing the impact of lipoprotein (a) lowering with pelacarsen (TQJ230) on major cardiovascular events in patients with established cardiovascular disease - CTQJ230A12301

ovartis Pharma AG0 个研究点目标入组 8,323 人开始时间: 2024年3月26日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
8,323

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Lp(a) = 70 mg/dL at the screening visit, Optimal LDL-cholesterol lowering treatment, Optimal treatment of other CV risk factors, Myocardial infarction: = 3 months from screening and randomization visits to = 10 years prior to the screening visit, and/or, Ischemic stroke: = 3 months from screening and randomization visits to = 10 years prior to the screening visit, and/or, Clinically significant symptomatic peripheral artery disease

排除标准

  • Uncontrolled hypertension, Heart failure New York Heart Association (NYHA) class IV, History of malignancy of any organ system, History of hemorrhagic stroke or other major bleeding, Platelet count <140,000 per mm3, Active liver disease or hepatic dysfunction, Significant kidney disease, Pregnant or nursing women

研究者

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