EUCTR2018-000175-33-RO进行中（未招募）1 期
A Phase II, Randomised, Double-Blind, Placebo Controlled, Parallel-Group, Multicentre, Three Month Duration Potassium Reduction Initiative to Optimize RAAS Inhibition Therapy with Sodium Zirconium Cyclosilicate in Heart Failure (PRIORITIZE HF) - PRIORITIZE HF
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 182
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. Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
- •2. Provision of signed and dated, written informed consent form prior to any mandatory study specific procedures, sampling, and analyses.
- •3. Provision of signed and dated written genetic informed consent prior to collection of sample for genetic analysis. Individuals refusing to provide informed consent for genetic testing may still be included in the study, but will not have to provide samples for genetic analysis.
- •4. Subject must be =18 years of age inclusive, at the time of signing the informed consent form.
- •5. Individuals with established documented diagnosis of symptomatic Heart failure with reduced ejection fraction (HFrEF).
- •6. Individuals with left ventricular ejection fraction = 40%.
- •7. Individuals receiving background standard of care for HFrEF and treated according tolocally recognized guidelines with both drugs and devices, as appropriate.
- •8. Individuals at risk of developing hyperkalaemia during the study
- •9. Women of childbearing potential must have a negative pregnancy test during screening (before first dose of investigational product [IP]) performed locally.
- •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 140
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 140
排除标准
- •1. HF due to restrictive cardiomyopathy, active myocarditis, constrictive pericarditis,hypertrophic (obstructive) cardiomyopathy or uncorrected primary valvular disease.
- •2. Current acute decompensated HF, hospitalization due to decompensated HF within 4 weeks prior to enrolment, or myocardial infarction (MI), unstable angina, stroke or transient ischemic attack (TIA) within 12 weeks prior to enrolment.
- •3. Coronary revascularization or valvular repair/replacement within 12 weeks prior to enrolment or planned to undergo any of these operations after randomization.
- •4. Symptomatic hypotension or systolic blood pressure (BP) <95 mmHg on 2 consecutive measurements.
- •5. Receiving dialysis or anticipated by the investigator to require dialysis therapy within 3 months.
- •6. Prior history of hypersensitivity to a renin angiotensin aldosterone system inhibitor (RAASi) drug, including but not limited to development of angioedema, icterus, hepatitis, or neutropenia or thrombocytopenia requiring treatment modification.
- •7. Addison’s disease or other causes of hypoaldosteronism.
- •8. Known hypersensitivity to sodium zirconium cyclosilicate (ZS).
- •9. Any condition outside the cardiovascular (CV) and renal disease area, such as but not limited to malignancy, with a life expectancy of less than 2 years based on investigator´s clinical judgement.
- •10. Active malignancy requiring treatment.
- •11. Current treatment with mineralocorticoid receptor antagonist (MRA), including spironolactone, eplerenone, canrenone, canrenoate, or finerenone, at any dose at enrolment.
- •12. Treated with potassium binding resins such as sodium polystyrene sulfonate (SPS; e.g. Kayexalate®) or calcium polystyrene sulfonate (CPS; e.g. Resonium®) or the cation exchange polymer, patiromer sorbitex calcium (Veltassa®) within 7 days prior to the first dose of study drug.
- •13. Treated with potassium supplements within 7 days prior to randomization.
- •14. Participation in another clinical study with ZS at any time or treatment with any investigational product (IP) during the last 3 months.
- •15. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff, AstraZeneca representatives, and/or staff at the study site).
- •16. Judgment by the investigator that the subject should not participate in the study if the subject is unlikely to comply with study procedures, restrictions and requirements.
- •17. Previous randomisation in the present study.
研究者
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