此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Randomized Evaluation of Istaroxime for Stabilization in Acute Heart Failure-Cardiogenic Shock (RESCUE HF-CS)

2026年5月7日 更新者:Seismic Pharmaceuticals Operations LLC

A Randomized, Double-blind, Phase 2b/3 Clinical Study of Istaroxime Combined With Standard Care Versus Placebo and Standard of Care for the Treatment of Cardiogenic Shock (CS) Society for Cardiovascular Angiography and Interventions (SCAI) Stage B or C Due to Acute Heart Failure (AHF)

The goal of this clinical trial is to learn if the drug istaroxime works to treat mild to moderate cardiogenic shock due to acute heart failure in adults. It will also learn about the safety of istaroxime. The main questions it aims to answer are:

  • Does istaroxime relieve participants' shortness of breath compared to a placebo?
  • Does istaroxime provide clinical benefit in terms of lowering the risk of dying, having invasive procedures, having worsening heart failure, and/or increasing quality of life compared to a placebo?
  • Does istaroxime increase blood pressure compared to a placebo? Researchers will compare istaroxime to a placebo (a look-alike substance that contains no drug) to see if istaroxime works to treat mild to moderate cardiogenic shock due to acute heart failure.

Participants will:

  • Receive a 48-hour intravenous infusion of istaroxime or placebo
  • Complete questionnaires rating their breathing and describing their quality of life
  • Return for a visit 30 and 90 days after the initial drug infusion was started

研究概览

地位

尚未招聘

研究类型

介入性

注册 (估计的)

600

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Aged between 18 and 80 years old (inclusive) at the time of informed consent, regardless of gender.
  2. Diagnosed with CS SCAI B or C due to AHF during screening, before randomization, as defined by:

    1. Dyspnea at rest or with minimal activity before screening and randomization.
    2. Pulmonary rales, or lower limb edema by physical examination.
    3. Evidence of pulmonary congestion by chest X-ray, CT scan or lung ultrasound
    4. At the time of screening and just prior to randomization either:

      1. systolic BP ≤ 100 mmHg or
      2. systolic BP ≤ 115 mmHg and >100 mmHg accompanied by at least one sign of hypoperfusion or hemodynamic compromise: cool extremities, altered mentation attributable to low output, oliguria, elevated lactate (>2 mmol/L), worsening renal function attributable to low perfusion, or invasive/noninvasive hemodynamic evidence of reduced cardiac output.
  3. Admitted for AHF within 20 hours before randomization.
  4. Documented history within 6 months prior to screening, or during the current admission, of left ventricular ejection fraction (LVEF) < 40%.
  5. New York Heart Association (NYHA) functional class ≥ II at 1 month prior to admission.
  6. N-terminal pro-B-type natriuretic peptide (NT-proBNP) > 1,500 pg/mL or BNP > 400 pg/mL during screening, before randomization.
  7. Signed informed consent as described in Section 11.3 which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

Exclusion Criteria:

  1. Body weight < 40 kg or ≥ 150 kg at Screening.
  2. Society for Cardiovascular Angiography and Interventions (SCAI) level D or more severe cardiogenic shock during screening, prior to randomization.
  3. Patients with any systolic blood pressure measurement >130 mmHg within 2 hours prior to randomization.
  4. Administration during the 6 hours prior to screening of vasodilators such as nitroglycerin, nitrates, recombinant human brain natriuretic peptide
  5. Prescription of digoxin within 7 days before randomization.
  6. Patients with severe lung disease (dependent on oral steroids or immunosuppressive therapy or require home oxygen therapy), respiratory failure, or severe pulmonary hypertension.
  7. Acute ischemic or hemorrhagic cerebral infarction or transient ischemic attack within 30 days before screening.
  8. Abnormal laboratory findings including during screening:

    1. Renal impairment (eGFR < 25 ml/min/1.73 m2) or the need for long-term or intermittent renal support therapy (hemodialysis, ultrafiltration or peritoneal dialysis);
    2. Severe electrolyte imbalance (Na+ <120mmol/L or >160mmol/L, and/or K+ <3.2mmol/L or >5.5mmol/L);
    3. Liver function impairment (ALT and/or AST > 3 times the upper limit of the normal range and/or bilirubin exceeds 1.5 times the upper limit of the normal range);
    4. Hemoglobin <9 g/dL (<5.6 mmol/L).
  9. Severe valvular stenosis that has not been surgically corrected, or moderate or severe aortic or pulmonary regurgitation.
  10. Obstructive hypertrophic cardiomyopathy or restrictive cardiomyopathy, constrictive pericarditis, cardiac tamponade, cardiomyopathy based on infiltrative disease (such as amyloidosis), accumulation disease (such as hemochromatosis, Fabry disease), myocardial dysplasia, cardiomyopathy caused by reversible causes (such as stress cardiomyopathy) or acute myocarditis.
  11. Sustained ventricular tachycardia or ventricular fibrillation within 30 days of screening and randomization.
  12. Significant bradycardia (sustained ventricular rate <50 beats per minute), or second or third-degree atrioventricular block (except those using permanent pacemakers).
  13. Type 1 acute coronary syndrome (ACS)/myocardial infarction (MI) in the 30 days prior to screening inclusive of the current admission.
  14. Patients who have undergone percutaneous coronary angiography or coronary artery bypass grafting or other major cardiovascular surgery including ICD and / or CRT or mechanical support devices within one month before screening, or patients who are expected to require revascularization within three months after screening.
  15. Patients on mechanical circulatory support (MCS) during Screening or at the time of randomization.
  16. Patients who are expected to require heart transplantation or left ventricular assist during the study period.
  17. Patients diagnosed with malignant tumors within 1 year before signing the informed consent form or at the time of screening (excluding fully treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, localized prostate cancer after radical surgery, and breast ductal carcinoma in situ after radical surgery), or those undergoing anti-tumor treatment at the time of screening.
  18. Patients with diseases that in the opinion of the investigator may lead to mortality within 90 days from randomization.
  19. Patients who suffer from severe mental or psychological disorders, cognitive impairment, or a history of mental illness.
  20. Patients with known severe allergies or a history of severe drug or food allergic reactions, or those known to be allergic to Istaroxime or its ingredients including lactose.
  21. Patients who are pregnant, breastfeeding or planning pregnancy.
  22. Patients who cannot be guaranteed to take effective contraceptive measures from the time of signing the informed consent to the 30 days following their last exposure to study drug, or who are of childbearing potential and plan to donate sperm/eggs during this period.
  23. Patients of childbearing potential without a negative highly sensitive serum pregnancy test within 24 hours before the first dose of trial intervention.
  24. Patients participating in other clinical studies and/or received other study intervention (study drugs or medical devices, etc.) within 30 days before signing the informed consent form, or who are still in the follow up period of other clinical studies.
  25. Patients who are unable to comply with all study requirements.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
intravenous placebo
实验性的:istaroxime
intravenous istaroxime

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in systolic BP
大体时间:24 hours
24 hours
composite outcome
大体时间:30 days
Hierarchical composite of death, mechanical circulatory support, worsening heart failure, quality of life assessed using the 'win ratio' method. Quality of life measured on a scale from 0=worst to 100=best. Measured using the percentage of wins among all possible comparisons between patients.
30 days
shortnes of breath
大体时间:24 hours
Measured on a scale from 0=worst to 100=best breathing
24 hours

次要结果测量

结果测量
大体时间
lenght of hospital stay
大体时间:30 days
30 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月1日

初级完成 (估计的)

2028年12月1日

研究完成 (估计的)

2028年12月1日

研究注册日期

首次提交

2026年5月1日

首先提交符合 QC 标准的

2026年5月7日

首次发布 (实际的)

2026年5月13日

研究记录更新

最后更新发布 (实际的)

2026年5月13日

上次提交的符合 QC 标准的更新

2026年5月7日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅