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RecruitingNCT05672836ENAVO-TAVRUpdated Jun 29, 2026

ENAVOgliflozin Outcome Trial in Patients With Severe Aortic Stenosis After Transcatheter Aortic Valve Replacement

A Phase 4 interventional study of Enavogliflozin and Standard-of-Care in Aortic Valve Stenosis and Heart Failure, sponsored by Duk-Woo Park, MD. Recruiting at 31 sites in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-06-29.

Sponsored by Duk-Woo Park, MD · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
1,040
Allocation
Randomized
Ages
19 Years and older
Sex
All
01

Study summary

The goal of this trial is to to determine whether use of a novel SGLT2 inhibitor, Enavogliflozin 0.3 mg once daily is superior to placebo, when added to standard-of-care, in reducing the composite of major cardiovascular events and Heart Failure events (hospitalization for Heart Failure or urgent Heart Failure visit) among patients who underwent transcatheter aortic valve replacement for severe aortic stenosis and with heart failure with preserved ejection fraction.

02

Conditions studied

  • Aortic Valve Stenosis
  • Heart Failure

Keywords

  • Transcatheter Aortic Valve Implantation
  • heart failure with preserved ejection fraction
  • Sodium-glucose cotransporter-2 inhibitor
  • transcatheter aortic valve replacement
03

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

1. Patients aged ≥19 with symptomatic aortic stenosis who underwent successful transcatheter aortic valve replacement (TAVR)* (either native valve or valve in valve with any approved/marketed device).

* A successful TAVI is defined as device success according to the VARC-2(Valve Academic Research Consortium 2) and VARC-3 criteria:

  1. correct positioning of a single prosthetic heart valve into the proper anatomical location AND
  2. intended performance of the prosthetic heart valve (mean aortic valve gradient \<20 mmHg, peak velocity \<3 m/s, no moderate or severe prosthetic valve regurgitation) AND
  3. absence of periprocedural complications (any type of stroke, life-threatening bleeding, acute coronary artery obstruction requiring intervention, major vascular complication requiring intervention, unresolved acute valve thrombosis, or any requirement of a repeat procedure).

2. Heart Failure with Mildly Reduced or Preserved Ejection Fraction

  1. Left ventricular ejection fraction (LVEF) ≥40%
  2. structural heart disease_Left ventricular hypertrophy (LVH) or Left atrial enlargement

    A. Left ventricular hypertrophy (LVH) with septal thickness or posterior wall thickness ≥ 1.1 cm or

    B. Left atrial (LA) enlargement with at least one of the following: LA width (diameter) ≥3.8 cm or LA length ≥ 5.0 cm, or LA area ≥ 20cm2, or LA volume ≥ 55mL or LA volume index ≥ 29mL/m.

  3. NT-proBNP ≥ 300 pg/mL (for patients without ongoing atrial fibrillation) or NT-proBNP must be ≥ 600 pg/mL (for patients with ongoing atrial fibrillation).

3. Patients who voluntarily participated in the written agreement

Exclusion criteria

Exclusion Criteria:

  1. Acute decompensated Heart Failure (exacerbation of chronic Heart Failure) requiring intravenous diuretics, vasodilators, inotropic agents, or mechanical support, or hemodynamic instability following the transcatheter aortic valve replacement procedure.
  2. Currently receiving therapy with an SGLT2 inhibitor within 4 weeks prior to randomization; discontinuation of current use of SGLT2 inhibitor for the purposes of study enrolment is not permitted.
  3. Known allergy, hypersensitivity, or previous intolerance to an SGLT2 inhibitors.
  4. HF with reduced ejection fraction (LVEF \<40%).
  5. Type 1 diabetes mellitus or diabetes ketoacidosis.
  6. Chronic cystitis and/or recurrent urinary tract infection (≥2 times within 1 year).
  7. Stroke or transient ischemic attack within 12 weeks prior to enrollment.
  8. Symptomatic persistent hypotension and/or a systolic blood pressure (SBP) \< 95 mm Hg at screening or at randomization.
  9. SBP ≥180 mmHg irrespective of treatment or SBP ≥160 mmHg with at least ≥3 antihypertensive drugs at screening or randomization.
  10. Heart failure due to any of the following causes; known infiltrative cardiomyopathy (e.g. amyloid, sarcoid, lymphoma, endomyocardial fibrosis, haemochromatosis, Fabry disease), active myocarditis, constrictive pericarditis, cardiac tamponade, known hypertrophic obstructive cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD), or uncorrected primary valvular disease.
  11. Severe renal insufficiency (eGFR \<30 ml/min/1.73 m2 of body-surface area based on the Modification of Diet in Renal Disease (MDRD) formula) or end-stage renal disease or requiring dialysis at the time of screening.
  12. Acute or chronic liver disease with severe impairment of liver function (e.g., ascites, esophageal varices, coagulopathy) or serum levels of transminases or alkaline phosphatase more than two times the upper limit of normal at screening.
  13. Chronic pulmonary disease requiring home oxygen, oral steroid therapy or hospitalization for exacerbation within 12 months, or significant chronic pulmonary disease in the Investigator's opinion, or primary pulmonary arterial hypertension.
  14. Current or suspicious malignancy or history of malignancy within 5 years
  15. Uncontrolled anaemia or haemoglobin \<9g/dl
  16. Uncontrolled hypothyroidism or arrhythmia or tachycardia
  17. Current ongoing alcoholic or drug addict
  18. Subjects with non-cardiac co-morbidities with life expectancy less than 12 months
  19. Planned major high-risk operation after transcatheter aortic valve replacement (TAVR)
  20. Women of childbearing age who have not reached a consensus on the use of highly effective contraception. Pregnancy or breastfeeding.
  21. Participation in other clinical trials, However, where at least one or more conditions are satisfied, it could be an exception according to an investigator's discretion;

    • Participating in the observational study expected no effect on the safety and/or effectiveness evaluation of this trial.
    • Screening failed before any interventional factor is involved.
    • Participants who have completed their involvement in clinical trials and have surpassed a 4-week period since their last administration of the investigational drug.
    • Participated in academic trials like strategic or medical device comparison studies conducted under standard therapy provided that there is no additional risk or a specific procedure to a subject and no interference between this trial and other studies.
04

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
1,040 participants (estimated)

Study arms

  • Experimental
    Enavogliflozin Group

    0.3 mg 1 tablet once daily

    Drug: Enavogliflozin

  • Placebo comparator
    placebo as add-on to standard of care treatment group

    Placebo matching enavogliflozin

    Drug: Standard-of-Care

Interventions

  • DrugEnavogliflozin

    0.3 mg 1 tablet once daily

  • DrugStandard-of-Care

    Standard-of-Care medical therapy plus Enavogliflozin matching placebo

    Also known as: Standard-of-Care medical therapy

05

What researchers measure

Primary outcomes

  1. Time from randomization to first occurrence of a composite of major adverse cardiovascular events* or hospitalization for heart failure

    Time from randomization to the first occurrence of a composite of major adverse cardiovascular events\* or hospitalization for heart failure at 12 months after randomization. \*Major adverse cardiovascular events included death from any causes, nonfatal myocardial infarction, or nonfatal stroke. A composite endpoint is an endpoint that is a combination of multiple clinical endpoints. An event is considered to have occurred if any one of several different events is observed.

    Time frame: 12 months

Secondary outcomes

  1. Event rate of death from any cause

    Time frame: 12 months

  2. Event rate of nonfatal myocardial infarction

    Time frame: 12 months

  3. Event rate of nonfatal stroke

    Time frame: 12 months

  4. Event rate of hospitalization for heart failure

    Time frame: 12 months

  5. Event rate of Composite renal endpoint

    Composite renal endpoint, defined as time to first occurrence of (1) chronic dialysis; (2) renal transplantation; (3) sustained reduction of ≥40% in estimated glomerular filtration rate (GFR); or (4) sustained estimated GFR \<15 mL/min/1.73 m2 for patients with baseline estimated GFR ≥30 mL/min/1.73 m2.

    Time frame: 12 months

  6. Event rate of Rehospitalization for any reason

    Time frame: 12 months

  7. Changes in measures of cardiac volume and function assessed by serial echocardiography

    left ventricular ejection fraction(LVEF), LV end-diastolic volume index (LVEDVI), LV end-systolic volume index (LVESVI), left atrial volume index (LAVI), and the ratio of early transmitral Doppler velocity/early diastolic annular velocity (E/e')

    Time frame: 12 months

  8. Changes in New York Heart Association (NYHA) functional class and the Kansas City Cardiomyopathy Questionnaire (KCCQ) summary score

    New York Heart Association (NYHA) Functional Classification on a scale from I to IV, with higher scores indicating severe symptoms and physical limitations associated with heart failure. the Kansas City Cardiomyopathy Questionnaire (KCCQ)on a scale from 0 to 100, with higher scores indicating fewer symptoms and physical limitations associated with heart failure.

    Time frame: 12 months

  9. Serial change in NT-proBNP

    N-terminal (NT)-pro hormone BNP (NT-proBNP)

    Time frame: 12 months

  10. Event rate of the safety events

    The safety events are defined as; * Serious adverse events * Adverse events leading to treatment discontinuation * Adverse events of special interest(AESI) * Hypoglycemia, genitourinary infections, hepatic injury, decreased renal function, ketoacidosis, events leading to lower limb amputation * AESIs leading to treatment discontinuation

    Time frame: 12 months

06

Study locations

28 of 31 sites recruiting
  • Bucheon Sejong Hospital
    Bucheon-si, South Korea
    • Young-jin Choi, MD · Contact
    • Young-jin Choi, MD · Principal investigator
    Recruiting
  • Gyeongsang National University Changwon Hospital
    Changwon, South Korea
    • Jae-seok Bae, MD · Contact
    • Jae-seok Bae, MD · Principal investigator
    Recruiting
  • Daegu Catholic University Medical Center
    Daegu, South Korea
    • Jin-bae Lee, MD · Contact
    • Jin-bae Lee, MD · Principal investigator
    Recruiting
  • Keimyung University Dongsan Medical Center
    Daegu, South Korea
    • Chul-hyun Lee, MD · Contact
    • Chul-hyun Lee, MD · Principal investigator
    Recruiting
  • Kyungpook National University Hospital
    Daegu, South Korea
    • Dong-heon Yang, MD · Contact
    • Dong-heon Yang, MD · Principal investigator
    Recruiting
  • Yeungnam University Medical Center
    Daegu, South Korea
    Withdrawn
  • Chungnam National University Hospital
    Daejeon, South Korea
    • Jin-Ok Jeong, MD · Contact
    • Jin-Ok Jeong, MD · Principal investigator
    Recruiting
  • The Catholic University of Korea, Daejeon ST. Mary's Hospital
    Daejeon, South Korea
    • Man-won Park, MD · Contact
    • Man-won Park, MD · Principal investigator
    Recruiting
  • Gangneung Asan Hospital
    Gangneung, South Korea
    • Han-bit Park, MD · Contact
    • Han-bit Park, MD · Principal investigator
    Recruiting
  • Chonnam National University Hospital
    Gwangju, South Korea
    • Ju-han Kim, MD · Contact
    • Ju-han Kim, MD · Principal investigator
    Recruiting
  • Inje University Ilsan Paik Hospital
    Ilsan, South Korea
    • Seong-wook Kwon, MD · Contact
    • Seong-wook Kwon, MD · Principal investigator
    Recruiting
  • Gachon University Gil Hospital
    Incheon, South Korea
    • Woong-cheol Kang, MD · Contact
    • Woong-cheol Kang, MD · Principal investigator
    Recruiting
  • Incheon Sejong Hospital
    Incheon, South Korea
    • Rak-kyoung Choi, MD · Contact
    • Rak-kyoung Choi, MD · Principal investigator
    Recruiting
  • Inha University Hospital
    Incheon, South Korea
    • Sang-don Park, MD · Contact
    • Sang-don Park, MD · Principal investigator
    Recruiting
  • The Catholic University of Korea, Incheon St. Mary's Hospital
    Incheon, South Korea
    • Ik-joon Choi, MD · Contact
    • Ik-joon Choi, MD · Principal investigator
    Recruiting
  • Dong-A Medical Center
    Pusan, South Korea
    • Yong-rak Cho, MD · Contact
    • Yong-rak Cho, MD · Principal investigator
    Recruiting
  • Inje University Pusan Paik Hospital
    Pusan, South Korea
    • Tae-hyun Yang, MD · Contact
    • Tae-hyun Yang, MD · Principal investigator
    Recruiting
  • Pusan National University Hospital
    Pusan, South Korea
    • Jung-Hyun Choi, MD · Contact
    • Jung-Hyun Choi, MD · Principal investigator
    Recruiting
  • Seoul university Bundang hospital
    Seongnam-si, South Korea
    • In-ho Chae, MD · Contact
    • In-ho Chae, MD · Principal investigator
    Recruiting
  • Asan Medical Center
    Seoul, South Korea
    • Duk-woo Park, MD · Contact
    • Duk-woo Park, MD · Principal investigator
    Recruiting
  • Ewha Womans University Mokdong Hospital
    Seoul, South Korea
    • In-sook Kang, MD · Contact
    • In-sook Kang, MD · Principal investigator
    Recruiting
  • Ewha Womans University Seoul Hospital
    Seoul, South Korea
    • Sang-hoon Shin, MD · Contact
    • Sang-hoon Shin, MD · Principal investigator
    Recruiting
  • Hanyang University Seoul Hospital
    Seoul, South Korea
    • Hyungdon Kook, MD · Contact
    • Hyungdon Kook, MD · Principal investigator
    Recruiting
  • Konkuk University Medical Center
    Seoul, South Korea
    • Bum-seong Kim, MD · Contact
    • Bum-seong Kim, MD · Principal investigator
    Recruiting
  • Korea University Anam Hospital
    Seoul, South Korea
    • Chul-woong Yoo, MD · Contact
    • Chul-woong Yoo, MD · Principal investigator
    Recruiting
  • Korea University Guro Hospital
    Seoul, South Korea
    • Cheol-ung Choi, MD · Contact
    • Cheol-ung Choi, MD · Principal investigator
    Recruiting
  • SNU Boramae Medical Center
    Seoul, South Korea
    • Woo-young Jeong, MD · Contact
    • Woo-young Jeong, MD · Principal investigator
    Recruiting
  • The Catholic Univ. of Korea Eunpyeong St. Mary's hospital
    Seoul, South Korea
    • Jeong-hoon Lee, MD · Contact
    • Jeong-hoon Lee, MD · Principal investigator
    Recruiting
  • The Catholic University of Korea, ST. Vincent's Hospital
    Suwon, South Korea
    Withdrawn
  • Uijeongbu Eulji Medical Center, Eulji University
    Uijeongbu-si, South Korea
    Withdrawn
  • Ulsan University Hospital
    Ulsan, South Korea
    • Kyoung-min Park, MD · Contact
    • Kyoung-min Park, MD · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05672836
Lead sponsor
Duk-Woo Park, MD
Collaborators
CardioVascular Research Foundation, Korea, Daewoong Pharmaceutical Co. LTD.
Responsible party
Duk-Woo Park, MD (Professor, Cardiology, Asan Medical Center Heart Institute, Valvular Heart Disease Center, Ischemic Heart Disease Center, Asan Medical Center) — Sponsor-investigator
First posted
Jan 5, 2023
Start date
Dec 18, 2024
Primary completion
Dec 2028 (estimated)
Completion
Apr 2029 (estimated)
Last update
Jun 29, 2026

Study contacts

Jeong-youn Bae, Project manager
Contact
cvcrc10@amc.seoul.kr
82230107259
Seung-jung Park, MD
study chair · Professor, Cardiology, Asan Medical Center Heart Institute, Valvular Heart Disease Center, Ischemic Heart Disease Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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