- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07583446
Randomized Evaluation of Istaroxime for Stabilization in Acute Heart Failure-Cardiogenic Shock (RESCUE HF-CS)
2026년 5월 7일 업데이트: 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
연구 개요
연구 유형
중재적
등록 (추정된)
600
단계
- 2 단계
- 3단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Gad Cotter MD, MD
- 전화번호: 9195990939
- 이메일: gadcotter@seismicrx.com
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- Aged between 18 and 80 years old (inclusive) at the time of informed consent, regardless of gender.
Diagnosed with CS SCAI B or C due to AHF during screening, before randomization, as defined by:
- Dyspnea at rest or with minimal activity before screening and randomization.
- Pulmonary rales, or lower limb edema by physical examination.
- Evidence of pulmonary congestion by chest X-ray, CT scan or lung ultrasound
At the time of screening and just prior to randomization either:
- systolic BP ≤ 100 mmHg or
- 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.
- Admitted for AHF within 20 hours before randomization.
- Documented history within 6 months prior to screening, or during the current admission, of left ventricular ejection fraction (LVEF) < 40%.
- New York Heart Association (NYHA) functional class ≥ II at 1 month prior to admission.
- N-terminal pro-B-type natriuretic peptide (NT-proBNP) > 1,500 pg/mL or BNP > 400 pg/mL during screening, before randomization.
- 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:
- Body weight < 40 kg or ≥ 150 kg at Screening.
- Society for Cardiovascular Angiography and Interventions (SCAI) level D or more severe cardiogenic shock during screening, prior to randomization.
- Patients with any systolic blood pressure measurement >130 mmHg within 2 hours prior to randomization.
- Administration during the 6 hours prior to screening of vasodilators such as nitroglycerin, nitrates, recombinant human brain natriuretic peptide
- Prescription of digoxin within 7 days before randomization.
- Patients with severe lung disease (dependent on oral steroids or immunosuppressive therapy or require home oxygen therapy), respiratory failure, or severe pulmonary hypertension.
- Acute ischemic or hemorrhagic cerebral infarction or transient ischemic attack within 30 days before screening.
Abnormal laboratory findings including during screening:
- 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);
- Severe electrolyte imbalance (Na+ <120mmol/L or >160mmol/L, and/or K+ <3.2mmol/L or >5.5mmol/L);
- 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);
- Hemoglobin <9 g/dL (<5.6 mmol/L).
- Severe valvular stenosis that has not been surgically corrected, or moderate or severe aortic or pulmonary regurgitation.
- 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.
- Sustained ventricular tachycardia or ventricular fibrillation within 30 days of screening and randomization.
- Significant bradycardia (sustained ventricular rate <50 beats per minute), or second or third-degree atrioventricular block (except those using permanent pacemakers).
- Type 1 acute coronary syndrome (ACS)/myocardial infarction (MI) in the 30 days prior to screening inclusive of the current admission.
- 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.
- Patients on mechanical circulatory support (MCS) during Screening or at the time of randomization.
- Patients who are expected to require heart transplantation or left ventricular assist during the study period.
- 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.
- Patients with diseases that in the opinion of the investigator may lead to mortality within 90 days from randomization.
- Patients who suffer from severe mental or psychological disorders, cognitive impairment, or a history of mental illness.
- 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.
- Patients who are pregnant, breastfeeding or planning pregnancy.
- 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.
- Patients of childbearing potential without a negative highly sensitive serum pregnancy test within 24 hours before the first dose of trial intervention.
- 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.
- Patients who are unable to comply with all study requirements.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
위약 비교기: 위약
|
intravenous placebo
|
|
실험적: istaroxime
|
intravenous istaroxime
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in systolic BP
기간: 24 hours
|
24 hours
|
|
|
composite outcome
기간: 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
기간: 24 hours
|
Measured on a scale from 0=worst to 100=best breathing
|
24 hours
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
lenght of hospital stay
기간: 30 days
|
30 days
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
2026년 7월 1일
기본 완료 (추정된)
2028년 12월 1일
연구 완료 (추정된)
2028년 12월 1일
연구 등록 날짜
최초 제출
2026년 5월 1일
QC 기준을 충족하는 최초 제출
2026년 5월 7일
처음 게시됨 (실제)
2026년 5월 13일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 5월 13일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 5월 7일
마지막으로 확인됨
2026년 5월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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