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Heart TransplantPhase 4NCT06625073

Randomized Trial of SGLT2i in Heart Transplant Recipients

A Phase 4 study testing Empagliflozin in people with Heart Transplant and Cardiovascular Disease, run by VA Office of Research and Development at 6 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Heart transplant (HTx) is an established therapy for advanced heart disease that restores quality of life and improves survival. However, due to preexisting comorbidities combined with the immunosuppressive therapies required after transplantation, HTx recipients remain at high risk for kidney, cardiovascular (CV)… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Empagliflozin
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
200 participants
Where
6 sitesUnited States
Study dates
20 Jan 2026to 28 Feb 2030
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 years or older
  • Heart transplant recipient, 3 months after transplant

Who cannot join

  • eGFR <20 mL/min/1.73m2
  • Type 1 diabetes mellitus
  • HbA1C >10%
  • Baseline UACR <30 mg/g in patients without T2D
  • Known allergy or intolerance to SGLT2i
  • Active uncontrolled infection
Show all 9Show fewer
  • Multiorgan transplant
  • SGLT2i treatment in the last 30 days
  • Pregnancy, breast-feeding or woman of child-bearing age not on birth control

Trial locations and contacts

6 sites in 1 country. Contact the study team or a site near you to ask about taking part.

6 sites in 1 country

United States6 sites, 6 recruiting
  • Michael E. DeBakey VA Medical Center, Houston, TX

    Houston, Texas, 77030-4211

    Savitri E Fedson, MD, 713-791-1414, savitri.fedson@va.gov

    Not yet recruiting
  • William S. Middleton Memorial Veterans Hospital, Madison, WI

    Madison, Wisconsin, 53705-2254

    David R Murray, MD, 608-256-1901, david.murray@va.gov

    Not yet recruiting
  • Tennessee Valley Healthcare System Nashville Campus, Nashville, TN

    Nashville, Tennessee, 37212-2637

    Henry Ooi, MD, 615-327-4751, henry.ooi@va.gov

    Not yet recruiting
  • VA Palo Alto Health Care System, Palo Alto, CA

    Palo Alto, California, 94304-1207

    Karim Sallam, MD, 650-493-5000 ext. 61848, Karim.Sallam@va.gov

    Not yet recruiting
  • Hunter Holmes McGuire VA Medical Center, Richmond, VA

    Richmond, Virginia, 23249-0001

    Neil Lewis, MD, 804-675-5000, neil.lewis@va.gov

    Not yet recruiting
  • VA Salt Lake City Health Care System, Salt Lake City, UT

    Salt Lake City, Utah, 84148-0001

    Heather Hanson, AAS BS, 801-582-1565 ext. 4543, Heather.Hanson@va.gov

    Josef Stehlik, MD MPH

    Recruiting

Other trials in United States

About this study

Official title: Randomized Trial of Sodium-glucose Cotransporter 2 Inhibition in Heart Transplant Recipients

Heart transplant (HTx) is an established therapy for advanced heart disease that restores quality of life and improves survival. However, due to preexisting comorbidities combined with the immunosuppressive therapies required after transplantation, HTx recipients remain at high risk for kidney, cardiovascular (CV), and metabolic disease. Large randomized clinical trials have recently shown that sodium-glucose cotransporter 2 inhibitors (SGLT2i) have potent kidney protective and CV benefits in many populations of patients with chronic kidney disease (CKD), CV disease and/or diabetes. SGLT2i have not been studied prospectively in HTx recipients, which represents a barrier to their use in this population.

In this multicenter randomized controlled trial in Veterans with HTx, investigators will evaluate the potential benefits of empagliflozin on kidney function, cardiometabolic risk, erythropoiesis, and functional status. A total of 200 Veterans will be randomly assigned to receive either empagliflozin 10 mg daily or a matching placebo for 12 months.

Read the detailed description

Heart transplant (HTx) markedly improves patient health-related quality of life (hrQoL) and survival in advanced heart failure (HF). However, HTx recipients remain at elevated risk for kidney and cardiovascular (CV) morbidity and mortality. Mitigating the negative effects of these morbidities on long-term survival and on patient hrQoL after HTx is a critical unmet need. Large clinical trials have recently shown that sodium glucose cotransporter 2 inhibitors (SGLT2i) have potent kidney protective and CV benefits. By preventing glucose reabsorption in the renal proximal tubule and promoting glycosuria, SGLT2i trigger multiple downstream effects, including improvement in insulin sensitivity and in mitochondrial efficiency in kidney and heart. SGLT2i also modulate sympathetic activity, improve endothelial function and reduce inflammation, with resultant improvement in myocardial and vascular function. SGLT2i increase erythropoietin levels and improve iron utilization. HTx is often complicated by development of chronic kidney disease (CKD), diabetes mellitus (T2D), anemia, and CV events, especially cardiac allograft vasculopathy (CAV). Although SGLT2i may significantly reduce development of these complications, prospective studies of SGLT2i did not include transplant recipients, leaving an important knowledge gap. HTx recipients could derive particularly significant benefits from SGLT2i therapy. The investigators hypothesize that SGLT2i with empagliflozin in HTx recipients will result in beneficial effects on kidney function, cardiometabolic risk, erythropoiesis and functional status, and that SGLT2i use in this population will be safe and well tolerated. The specific aims of this study are:

Specific Aim 1. Investigate the effects of SGLT2i with empagliflozin on kidney function in HTx recipients.

Kidney disease after HTx is a potent predictor of mortality. Investigators hypothesize that treatment with empagliflozin will preserve kidney function after HTx.

Aim 1a. Assess the effects of SGLT2i on urinary albumin-to-creatinine ratio (UACR). Albuminuria, represented by UACR and an independent predictor of kidney outcomes, was consistently reduced by SGLT2i in the landmark trials of SGLT2i. Approximately 50% of Veterans after HTx have at least moderate albuminuria. Investigators hypothesize that empagliflozin therapy will decrease albuminuria in HTx recipients.

Aim 1b. Assess the effect of SGLT2i on estimated glomerular filtration rate (eGFR).

SGLT2i therapy was associated with significantly slower decline of eGFR in all SGLT2i clinical trials of CKD. Investigators hypothesize that empagliflozin treatment will result in an improvement of eGFR slope in HTx recipients.

Specific Aim 2. Establish the safety and tolerability of SGLT2i therapy in HTx recipients.

SGLT2i have been tested prospectively in >75,000 patients and demonstrated a favorable safety profile. Exclusion of organ transplant recipients from these trials resulted in an important knowledge gap-the lack of safety and tolerability data in this population, which limits clinicians' use of SGLT2i in HTx recipients. Investigators hypothesize that treatment with empagliflozin in HTx recipients will be associated with favorable safety and tolerability.

Specific Aim 3. Evaluate the cardiometabolic, erythropoietic and functional effects of SGLT2i after HTx.

Cardiometabolic risks in HTx recipients contribute to CAV, graft failure, functional limitations and mortality. Investigators hypothesize that empagliflozin therapy will result in favorable cardiometabolic, erythropoietic and functional effects.

Aim 3a. Assess the effects of SGLT2i on markers of cardiometabolic risk.

Investigators will examine the effect of empagliflozin on hemoglobin A1c (HbA1c), body weight and blood pressure (BP), inflammation and on cardiac allograft health assessed through cardiac imaging and cardiac biomarkers. Investigators hypothesize that empagliflozin therapy will result in favorable cardiometabolic effects.

Aim 3b. Assess the effects of SGLT2i on erythropoiesis.

SGLT2i stimulates erythropoiesis, but the exact mechanisms are not well understood. Investigators hypothesize that empagliflozin will result in an increase in serum erythropoietin and amelioration of anemia in HTx recipients.

Aim 3c. Assess the effects of SGLT2i on functional status and health-related quality of life.

SGLT2i have improved functional status and hrQoL in non-transplant populations. Investigators hypothesize that the favorable kidney, cardiometabolic and erythropoietic effects of empagliflozin after HTx will result in a corresponding increase in six-minute walk test (6MWT) and hrQoL after transplant.

Being tested
Empagliflozin, Placebo
Keywords
Heart Transplant, Empagliflozin, Safety and Tolerability, Kidney Outcomes, Cardiometabolic Outcomes, Erythropoiesis, Functional Status, Quality of Life
Medical subject headings
Cardiovascular Diseases, Kidney Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • EmpagliflozinDrug

    Also called Jardiance

    A starting dose of empagliflozin 10 mg or matching placebo will be initiated after randomization and completion of the baseline testing. Participating subjects will remain at this dose for the whole study duration of 12 months.

  • PlaceboDrug

    Also called Control Group

    A starting dose of empagliflozin 10 mg or matching placebo will be initiated after randomization and completion of the baseline testing. Participating subjects will remain at this dose for the whole study duration of 12 months.

Study groups in NCT06625073
Study groupRoleWhat they receive
EmpagliflozinExperimentalA starting dose of empagliflozin 10 mg or matching placebo will be initiated after randomization and completion of the baseline testing. Participating subjects will remain at this dose for the whole study duration of 12 months.
Receives: Drug: Empagliflozin
PlaceboPlacebo comparatorA starting dose of empagliflozin 10 mg or matching placebo will be initiated after randomization and completion of the baseline testing. Participating subjects will remain at this dose for the whole study duration of 12 months.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Urinary albumin-to-creatinine ratio (UACR)

    UACR difference (mg/g) in subjects in active arm vs control arm

    Measured: 12 months

  2. Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

    Adverse and serious adverse events difference in active arm vs control arm

    Measured: 12 months

Secondary outcomes (17)
  1. Estimated Glomerular Filtration Rate (eGFR)

    eGFR difference (mL/min/1.73m2) in subjects in active arm vs control arm

    Measured: 12 months

  2. Hemoglobin A1c (HbA1c)

    HbA1c difference (%) in subjects in active arm vs control arm

    Measured: 12 months

  3. Fasting blood glucose

    Fasting blood glucose difference (mg/dL) in subjects in active arm vs control arm

    Measured: 12 months

  4. Body weight

    Body weight difference (kg) in subjects in active arm vs control arm

    Measured: 12 months

  5. Systolic and diastolic blood pressure

    Systolic and diastolic blood pressure difference (mmHg) in subjects in active arm vs control arm

    Measured: 12 months

  6. Serum high sensitivity C-reactive protein (hsCRP)

    Serum hsCRP difference (mg/L) in subjects in active arm vs control arm

    Measured: 12 months

  7. Serum N-Terminal Pro-B-Type Natriuretic Peptide (NTproBNP)

    Serum NTproBNP difference (pg/mL) in subjects in active arm vs control arm

    Measured: 12 months

  8. Hemoglobin

    Hemoglobin difference (g/dl) in subjects in active arm vs control arm

    Measured: 12 months

  9. Serum erythropoietin

    Serum erythropoietin difference (mU/mL) in active arm vs control arm

    Measured: 12 months

  10. Hematocrit

    Hematocrit difference (%) in active arm vs control arm

    Measured: 12 months

  11. Serum transferrin saturation

    Serum transferrin saturation difference (%) in active arm vs control arm

    Measured: 12 months

  12. Six Minute Walk Test

    Difference in distance (m) covered in the 6 minute walk test in active arm vs control arm

    Measured: 12 months

  13. Serum high sensitivity Troponin

    Serum high sensitivity Troponin difference (pg/mL) in subjects in active arm vs control arm

    Measured: 12 months

  14. Kansas City Cardiomyopathy Questionnaire-12

    Kansas City Cardiomyopathy Questionnaire-12 overall summary score difference in active arm vs control arm. Scale range 0-100. Higher result is better.

    Measured: 12 months

  15. Serum tumor necrosis factor -a (TNF-a)

    TNF-a difference (pg/mL) in subjects in active arm vs control arm

    Measured: 12 months

  16. Serum interleukin 6 (IL-6)

    IL-6 difference (pg/mL) in subjects in active arm vs control arm

    Measured: 12 months

  17. Serum interleukin 1b(IL-1b)

    IL-1b difference (pg/mL) in subjects in active arm vs control arm

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Oct 2024
  2. Study start20 Jan 2026
  3. Primary completion31 Aug 2029 (estimated)
  4. Study completion28 Feb 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Empagliflozin 10 ng daily for 12 months
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06625073
Sponsor's protocol ID
NEPH-004-24S
Status last verified
Jan 2026
First submitted
23 Sep 2024
Last updated
22 Jan 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Empagliflozin in people with Heart Transplant and Cardiovascular Disease, run by VA Office of Research and Development at 6 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 22 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Heather Hanson, AAS BS ((801) 582-1565 ext. 4543, Heather.Hanson@va.gov), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Urinary albumin-to-creatinine ratio (UACR) (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jan 2026.

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