EUCTR2021-006550-31-ES进行中（未招募）1 期
Efficacy and Security of BempeDoic acid in Acute Coronary Syndrome - ES-BempeDACS
SPANISH SOCIETY OF CARDIOLOGY0 个研究点目标入组 206 人开始时间: 2022年1月10日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 206
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Persistent LDL-C =70 mg/dl despite stable baseline regimen (=4 weeks) of high-potency statins, OR
- •2. LDL-C =100 mg/dl in patients who do not tolerate high-potency statins or who are not treated with high-potency statins, including statin-naïve patients.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 103
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 103
排除标准
- •1) Patients under 18 years of age, pregnant or breastfeeding.
- •2) Patients with absolute or relative contraindication to bempedoic acid or ezetimibe.
- •3) Patients with Triglycerides =400 mg / dL.
- •4) Patients treated with fibrates and/or PCSK9 inhibitor.
- •5) Patients with limited life expectancy (<1 year) at the judgment of the responsible physician.
- •6) Patients in another clinical trial.
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