EUCTR2010-022579-68-DE进行中(未招募)不适用
COR-1, an anti-ß1 receptor antibody cyclopeptide in heart failure: a phase II, multicentre, randomised, double-blind and placebo-controlled study with parallel groups - COR-1 in heart failure
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
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
- •- Diagnosed heart failure due to dilated cardiomyopathy
- •- presence of anti-ß1-adrenoreceptor autoantibodies in patients` blood samples
- •- LVEF < 45%, as determined by biplane echocardiography
- •- New York Heart Association (NYHA) class II – III
- •- disease duration: symptomatic heart failure for >1 year and <8 years
- •- Treatment with ACE inhibitors or angiotensin II receptor blockers (ARB), beta-blockers and aldosterone antagonists (the latter at the discretion of the attending physician) according to 2012 European Society of Cardiology guidelines for at least 6 months (with the exception of lack of tolerability of any of these drugs) and at stable doses for at least 2 months prior to screening (Note: standard therapy” can include, but does not have to include, any of the following: ACE inhibitor, angiotensin II receptor blockers (ARB) or beta-blocker.)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •- Ischemic heart disease characterised by = 50% coronary artery stenosis and/or history of myocardial infarction as determined by coronary angiography
- •- Third or higher degree valvular defect
- •- Clinically relevant disorder of the immune system (as determined by anamnesis)
- •- History of severe allergies, increased risk for anaphylactic shock (as determined by anamnesis e.g. bronchial asthma)
- •- Any disease requiring immunosuppressive drugs, except = 5 mg/day prednisone equivalent dose
研究者
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