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STEPwise De-escalation and Optimizing Withdrawal of ARNI and SGLT2i in Normalized Heart Failure (STEP-DOWN HF)

1 czerwca 2026 zaktualizowane przez: Kyungsub Song

STEPwise De-escalation and Optimizing Withdrawal of ARNI and SGLT2i in Normalized Heart Failure (STEP-DOWN HF Trial)

This is a multicenter, randomized, open-label pilot study to evaluate whether stepwise withdrawal of two heart failure medications-angiotensin receptor-neprilysin inhibitor (ARNI) and sodium-glucose cotransporter-2 inhibitor (SGLT2i)-is safe in patients with Heart Failure with improved Ejection Fraction (HFimpEF) whose underlying structural cause (valvular heart disease or ischemic cardiomyopathy) has been completely corrected by surgery or intervention.

Eighty adult patients (40 per arm) whose left ventricular ejection fraction (LVEF) has recovered to 50% or higher and whose NT-proBNP is below 250 ng/L will be randomized 1:1 to either (1) stepwise withdrawal of ARNI followed by SGLT2i over one month under close echocardiographic monitoring, or (2) continuation of their current guideline-directed medical therapy.

The primary outcome is the change in LVEF at 12 months, with non-inferiority of the withdrawal strategy declared if the LVEF decline is within 5 percentage points of the continuation arm. Secondary outcomes include cardiovascular death, heart failure hospitalization, NT-proBNP, quality of life (KCCQ-12), 6-minute walk distance, and adverse events.

Results from this pilot will inform the design and sample size of a subsequent definitive non-inferiority trial and may provide initial evidence to guide deprescribing decisions in clinical practice.

Przegląd badań

Szczegółowy opis

Background The 4-pillar guideline-directed medical therapy (GDMT) for heart failure-comprising ARNI, SGLT2i, mineralocorticoid receptor antagonists (MRA), and beta-blockers-is the established standard of care for patients with reduced ejection fraction. However, evidence guiding medication withdrawal in patients whose ejection fraction has normalized after correction of a reversible structural cause (HFimpEF) is lacking. The TRED-HF trial demonstrated that withdrawing GDMT in patients with idiopathic or familial dilated cardiomyopathy led to relapse in approximately 40% within six months. In contrast, WITHDRAW-AF, which enrolled patients whose tachycardia-induced cardiomyopathy resolved after successful catheter ablation, observed only 8.3% relapse, and CATHEDRAL-HF, which retained beta-blockers while withdrawing other agents, reported approximately 10% relapse. These findings suggest that selective, stepwise withdrawal in patients with fully corrected underlying disease may be safer than indiscriminate discontinuation.

Rationale for a Pilot Trial This pilot study addresses three objectives prior to a definitive non-inferiority trial: (1) primary safety assessment of a stepwise withdrawal protocol after structural correction; (2) feasibility of multicenter enrollment and follow-up; and (3) estimation of event rates and variance of the primary outcome to inform sample-size calculation for the subsequent confirmatory trial.

Study Design Multicenter, randomized, open-label, parallel-group pilot trial. Eighty patients will be randomized 1:1 to stepwise withdrawal or continuation, stratified by baseline NT-proBNP (≤50, 51-125, 126-250 ng/L) using a web-based central randomization system (Sealed Envelope). Five centers in the Republic of Korea will participate.

Intervention Stepwise Withdrawal Arm: ARNI is discontinued first. After one month of clinical and echocardiographic assessment, SGLT2i is discontinued only if there is no echocardiographic deterioration (LVEF drop <10 percentage points) and NT-proBNP remains ≤250 ng/L. MRA and beta-blockers, if present, are continued.

Continuation Arm: All current heart-failure medications, including ARNI and SGLT2i, are maintained per standard practice.

Safety Monitoring Two key safeguards are implemented: (1) a strictly sequential, stepwise withdrawal that prevents abrupt neurohormonal activation; and (2) mandatory transthoracic echocardiography at 1 and 3 months post-withdrawal to detect early subclinical deterioration before symptomatic relapse. This intensive echocardiographic surveillance distinguishes the protocol from prior trials, which relied primarily on serum biomarkers. Patients meeting predefined deterioration criteria (LVEF decline ≥10 percentage points from baseline, LVEF <40%, heart failure hospitalization, or emergency-department visit) are immediately reinstated on full GDMT and recorded as protocol withdrawal events. An independent Data and Safety Monitoring Board reviews safety data periodically.

Endpoints Primary Endpoint: Change in LVEF from baseline to 12 months. Non-inferiority is declared if the lower bound of the one-sided 95% confidence interval for the between-group difference exceeds -5 percentage points in the per-protocol population, with ITT analysis as a supportive analysis.

Secondary Endpoints: Composite of cardiovascular death and heart failure hospitalization at 12 months; absolute LVEF change; NT-proBNP change at 3 and 12 months; NYHA functional class change; KCCQ-12 quality-of-life score; 6-minute walk distance; incidence and severity of adverse events; and rate and timing of medication reinstatement.

Eligibility Adults (≥19 years) with a prior LVEF ≤40% that has recovered to ≥50% following complete surgical or interventional correction of valvular heart disease (mitral regurgitation, aortic stenosis, aortic regurgitation) or ischemic cardiomyopathy (PCI or CABG); NT-proBNP <250 ng/L at enrollment; receiving both ARNI and SGLT2i for at least three months; and no heart-failure hospitalization within the prior six months. Major exclusions include irreversible cardiomyopathy, incomplete revascularization, residual moderate or greater valvular regurgitation, eGFR <30 mL/min/1.73 m², symptomatic hypotension or bradycardia, pregnancy, and limited life expectancy.

Follow-up Scheduled visits at 1, 3, 6, 9, and 12 months. Assessments include vital signs, NT-proBNP, renal function, electrolytes, echocardiography (baseline, 1, 3, 6, 12 months), ECG, KCCQ-12, 6-minute walk test, and adverse event capture.

Statistical Analysis The pilot sample size of 40 per arm (total 80) is based on precision estimates for the primary outcome: assuming a 10% event rate, this yields approximately ±9.3% precision per arm and ±6.6% overall (Wilson method), which is adequate for variance estimation. A 15% drop-out rate is anticipated. All analyses will be conducted with SPSS and R.

Expected Contribution By generating the first prospective evidence on stepwise ARNI/SGLT2i withdrawal in patients with structurally corrected HFimpEF, this pilot trial aims to lay the methodological foundation for a definitive non-inferiority trial and ultimately to inform evidence-based deprescribing guidelines for this growing patient population.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

80

Faza

  • Faza 4

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

  • Nazwa: In Cheol Kim, Professor

Lokalizacje studiów

    • Daegu
      • Daegu, Daegu, Korea Południowa, 42601
        • Keimyung University Dongsan Hospital
    • Gyeonggi-do
      • Seongnam-si, Gyeonggi-do, Korea Południowa, 13620
        • Seoul National University Bundang Hospital
      • Suwon, Gyeonggi-do, Korea Południowa, 16499
        • Ajou University Hospital
    • Gyeongsangnam-do
      • Yangsan, Gyeongsangnam-do, Korea Południowa, 50612
        • Pusan National University Yangsan Hospital
        • Kontakt:
    • Seoul
      • Seoul, Seoul, Korea Południowa, 02841
        • Korea University Anam Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Adults aged 19 years or older
  • Prior left ventricular ejection fraction (LVEF) ≤40% before surgery or intervention, with recovery to ≥50% (normalized range) at the time of enrollment
  • N-terminal pro-B-type natriuretic peptide (NT-proBNP) <250 ng/L
  • Complete correction of a reversible underlying cause of heart failure: surgical or transcatheter correction of valvular heart disease (mitral regurgitation, aortic stenosis, aortic regurgitation), or percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) for ischemic cardiomyopathy
  • Currently receiving both ARNI and SGLT2i for at least 3 months at enrollment (MRA and/or beta-blocker may also be used)
  • Clinically stable outpatient with no heart failure-related hospitalization within the prior 6 months
  • Able to provide written informed consent

Exclusion Criteria:

  • Heart failure due to irreversible etiology (e.g., idiopathic dilated cardiomyopathy, toxic cardiomyopathy, genetic cardiomyopathy)
  • For valvular disease: moderate or greater paravalvular leak, or residual moderate or greater mitral or aortic regurgitation
  • For ischemic disease: incomplete revascularization or graft occlusion on post-operative coronary CT
  • Chronic kidney disease stage 4 or higher (eGFR <30 mL/min/1.73 m²)
  • Symptomatic hypotension (systolic blood pressure <90 mmHg) or symptomatic bradycardia (heart rate <50 beats/min)
  • Pregnant, suspected pregnancy, or breastfeeding
  • Terminal malignancy or end-stage organ failure with life expectancy <12 months
  • Participation in another clinical trial within 3 months prior to screening
  • Any condition that, in the investigator's judgment, makes the participant unsuitable for the study

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Stepwise Withdrawal
Stepwise discontinuation of ARNI followed by SGLT2i. ARNI is withdrawn first; if no echocardiographic deterioration (LVEF drop <10 percentage points) and NT-proBNP remains ≤250 ng/L after 1 month, SGLT2i is then withdrawn. MRA and beta-blockers, if previously prescribed, are continued. Intensive echocardiographic monitoring is performed at 1 and 3 months.
Sequential discontinuation of angiotensin receptor-neprilysin inhibitor (ARNI; e.g., sacubitril/valsartan) and sodium-glucose cotransporter-2 inhibitor (SGLT2i; e.g., dapagliflozin or empagliflozin). ARNI is discontinued first; after a 1-month observation with echocardiographic and biomarker assessment, SGLT2i is discontinued if no signs of deterioration are observed. Concomitant MRA and beta-blocker therapy is continued.
Aktywny komparator: Continuation
Continuation of all current heart-failure medications including ARNI and SGLT2i per guideline-directed medical therapy, with standard follow-up.
Continuation of currently prescribed ARNI and SGLT2i, together with any concomitant MRA and beta-blocker, at the doses being received at enrollment, per current guideline-directed medical therapy.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change in Left Ventricular Ejection Fraction (LVEF) at 12 Months
Ramy czasowe: Baseline to 12 months
Absolute change (percentage points) in LVEF from baseline to 12 months, measured by transthoracic echocardiography. Non-inferiority of stepwise withdrawal versus continuation is declared if the lower bound of the one-sided 95% confidence interval for the between-group difference exceeds -5 percentage points in the per-protocol population.
Baseline to 12 months

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Composite of Cardiovascular Death or Heart Failure Hospitalization
Ramy czasowe: Up to 12 months
Cumulative incidence of the composite endpoint of cardiovascular death or hospitalization for heart failure during the 12-month follow-up period.
Up to 12 months
Change in NT-proBNP
Ramy czasowe: Baseline to 12 months
Change from baseline in serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration at 3 and 12 months.
Baseline to 12 months
Change in NYHA Functional Class
Ramy czasowe: Baseline to 12 months
Change from baseline in New York Heart Association (NYHA) functional classification at 12 months.
Baseline to 12 months
Change in Quality of Life (KCCQ-12 Total Score)
Ramy czasowe: Baseline, 3 months, 6 months, 12 months
Change from baseline in the Kansas City Cardiomyopathy Questionnaire-12 (KCCQ-12) total score. Scores range from 0 to 100, with higher scores indicating better health status.
Baseline, 3 months, 6 months, 12 months
Change in 6-Minute Walk Distance
Ramy czasowe: Baseline, 6 months, 12 months
Change from baseline in the distance walked (in meters) during a standardized 6-minute walk test.
Baseline, 6 months, 12 months
Incidence and Severity of Adverse Events
Ramy czasowe: Up to 12 months
Frequency and severity of treatment-emergent adverse events and serious adverse events, including events specifically related to medication withdrawal (e.g., heart failure decompensation, hypotension, electrolyte abnormalities).
Up to 12 months
Rate and Timing of Medication Reinstatement
Ramy czasowe: Up to 12 months
Proportion of participants in the stepwise withdrawal arm requiring reinstatement of ARNI and/or SGLT2i due to clinical deterioration or protocol-defined criteria, and time from withdrawal to reinstatement.
Up to 12 months

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Śledczy

  • Główny śledczy: Hyung Gon Je, Professor, Seoul National University Bundang Hospital
  • Główny śledczy: Su Jin Park, Professor, Ajou University School of Medicine
  • Główny śledczy: Jun Ho Lee, Professor, Korea University Anam Hospital
  • Główny śledczy: Younju Rhee, Professor, Pusan National University Yangsan Hospital

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

30 czerwca 2026

Zakończenie podstawowe (Szacowany)

30 czerwca 2029

Ukończenie studiów (Szacowany)

30 grudnia 2029

Daty rejestracji na studia

Pierwszy przesłany

1 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

1 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

5 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

5 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

1 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • IRB number: 2026-04-022-003
  • RS-2026-25475665 (Inny numer grantu/finansowania: National Research Foundation of Korea)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIEZDECYDOWANY

Opis planu IPD

A decision regarding sharing of individual participant data (IPD) has not yet been made. The sponsor and steering committee will determine the IPD-sharing plan prior to the primary completion date, taking into account the requirements of journals selected for primary results publication, applicable Korean data-protection regulations (Personal Information Protection Act, Bioethics and Safety Act), and any conditions specified by the Institutional Review Board. If sharing is approved, de-identified IPD, the study protocol, statistical analysis plan, and informed consent form will be made available to qualified investigators upon reasonable request to the principal investigator.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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