Heart Transplant FailurePhase 3DAPARHTNCT05321706
DAPAgliflozin for Renal Protection in Heart Transplant Recipients
A Phase 3 study testing Dapagliflozin 10 mg in people with Heart Transplant Failure and Kidney Failure, run by Oslo University Hospital at 6 sites in 3 countries.
Trial summary
Kidney failure is common in heart transplant recipients and is a major cause of morbidity and mortality. Sodium-glucose transporter 2 (SGLT2) inhibitors were developed as antidiabetics but were subsequently shown to reduce the incidence of adverse cardiovascular outcomes and protect renal function in non-diabetics as… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Heart Transplant Failure, Kidney Failure
- What is being tested?
- Dapagliflozin 10 mg
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 430 participants
- Where
- 6 sitesin 3 countries
- Study dates
- 8 Jun 2022to 30 Nov 2028
- Phase
- Phase 3
- 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
- Heart transplant recipient ≥ 1 year after heart transplant.
- Age ≥ 18 years
Who cannot join
- Contraindications to study medication.
- Estimated GFR < 25 ml/min/m2
- Type I diabetes
- Severe liver failure (Child-Pugh's score C)
- Life expectancy reduced to < 2 years as judged by the investigator
- Unresolved malignant disease
Show all 11Show fewer
- Failure to obtain written informed consent
- SGL2 inhibitor treatment over the last month
- Pregnancy
- Breast-feeding
- Woman of child-bearing potential who is not willing to use a highly effective method of birth control
Trial locations and contacts
6 sites in 3 countries.
6 sites in 3 countries
Netherlands3 sites
University Medical Center Groningen
Groningen
Erasmus Medical Center
Rotterdam
University Medical Center Utrecht
Utrecht, 3584
Sweden2 sites
Skane University Hospital
Lund, 22185
Karolinska University Hospital
Stockholm
About this study
Official title: DAPARHT: DAPAgliflozin for Renal Protection in Heart Transplant Recipients
Kidney failure is common in heart transplant recipients and is a major cause of morbidity and mortality. Sodium-glucose transporter 2 (SGLT2) inhibitors were developed as antidiabetics but were subsequently shown to reduce the incidence of adverse cardiovascular outcomes and protect renal function in non-diabetics as well as diabetics. However, SGLT2 inhibitors have not been tested in clinical trials in heart transplant recipients. The DAPARHT trial is designed to assess the effect of the SGLT2 inhibitor dapagliflozin to prevent deteriorating renal function in heart transplant recipients. Secondary objectives are to assess the impact of treatment on i) weight, ii) glucose homeostasis, iii) proteinuria, iv) the number of rejections, and (v) safety and tolerability. As exploratory outcomes, the investigators will assess the effect of treatment on renal outcomes, clinical events (death, myocardial infarction, cerebral stroke, cancer, and end-stage renal disease), cardiac function, quality of life, and new-onset diabetes.
Read the detailed description
Heart transplant is the treatment of choice for selected patients with end-stage heart failure. Worldwide, approximately 5000 procedures are performed annually. Whereas the first successful heart transplant led to a mere 18 days' prolongation of the recipient's life, the median survival after transplantation is now more than 11 years. Important surgical advances, as well as optimal medical therapy, are responsible for this improvement, but reducing morbidity and mortality further is a significant challenge. Beyond the first year, outcomes have not improved over the last decades. An important reason for this is the considerable burden of long-term side effects induced by immunosuppressive therapy. Chronic renal failure occurs in approximately 11 % of heart transplant recipients during the first five years after transplant and is associated with a large increase in mortality. A major cause of renal injury is a calcineurin inhibitor (CNI)-related nephrotoxicity. Calcineurin inhibitors revolutionized transplant medicine when introduced in the early 1980'ies and remain the mainstay of immunosuppressive therapy after a heart transplant. However, the therapy is an important contributor to post-transplant nephropathy. Furthermore, CNIs seem to contribute to metabolic disturbances including diabetes mellitus, hypertension, and oxidative stress after a heart transplant.
The deterioration of renal function after a heart transplant appears to be linear. In a Swedish material, the average yearly drop in the estimated glomerular filtration rate (eGFR) was 2.2 ± 14.6 ml/min/1.73 m2. In the NOCTET trial, which comprised 282 Scandinavian heart and lung transplant recipients who were randomized to treatment with a CNI or low-dose CNI and everolimus 1-10 years after surgery, the measured glomerular filtration rate (GFR) declined 7.2 ml/min/1.73m2 during a mean follow up of 5.6 years (i.e. 1.3 ml/min/1.73m2 per year) independently of the time since transplantation and baseline GFR.
Proteinuria is an important determinant of ensuing renal failure. Approximately 25 % of patients listed for heart transplant have at least trace proteinuria. Of the investigators' maintenance heart transplant recipients, 18 % have manifest proteinuria defined as urine protein/creatinine ratio ≥ 30 mg/g. The median ratio is 49.5 mg/g (interquartile range 37-84), consistent with a daily loss of approximately 500 mg of protein in the urine.
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) inhibit glucose reuptake in the proximal tubules of the nephrons. They thereby cause loss of glucose in the urine and induce osmotic diuresis. SGLT2i have now been studied in several large placebo-controlled cardiovascular outcomes trials in patients with type 2 diabetes. These trials were performed to satisfy regulatory requirements, specifically to exclude the excess risk of cardiovascular death, myocardial infarction, or stroke, and to test for efficacy. Despite a modest reduction in glycated haemoglobin (HbA1c), all the trials so far have shown that SGLT2i robustly reduces the risk of hospitalization for heart failure and prevents the progression of kidney disease.
In the EMPA-REG OUTCOME trial, treatment with the SGLT-2 inhibitor empagliflozin resulted in a reduction of cardiovascular mortality of 38%. In addition, empagliflozin significantly reduced admissions for heart failure and the incidence of end-stage kidney disease. Among patients allocated to empagliflozin, the mean change in estimated GFR (eGFR) from baseline to follow-up after 3 years was 4.7 ml per minute per 1.73 m2 better than in patients allocated to placebo. However, immediately after starting the drug, the patients on active treatment experienced an apparent reduction in the eGFR. The curves did not cross until after the first year of treatment, where after a between-group difference was manifest in favor of empagliflozin. The event curves diverged right up to the end of the trial, and there was an additional increase in the difference in the eGFR between the active drug arm and the placebo arm after stopping the treatment, suggesting that while empagliflozin is indeed renoprotective in patients with type 2 diabetes, there is an on-treatment suppression of eGFR analogue to the effect produced by angiotensin-converting enzyme inhibitors/angiotensin II receptor antagonists.
The DECLARE-TIMI 58 trial showed that the SGLT-2 inhibitor dapagliflozin reduced the rate of cardiovascular death or hospitalization for heart failure in a manner consistent with the findings observed in the EMPA-REG trial. Dapagliflozin was also associated with a large reduction in the rate of progression to end-stage renal failure. In consistence with the data on empagliflozin, 6 months after randomization, the mean decrease in the estimated GFR was larger in the dapagliflozin group than in the placebo group. However, the mean change equalized by 2 years, and at 3 and 4 years the mean decrease in eGFR was less with dapagliflozin than with placebo. The absolute difference in eGFR was smaller than that observed in the EMPA-REG OUTCOMES trial; however, the inclusion criteria in the DECLARE-TIMI 58 trial ensured that most of the participants had normal kidney function at the start of the treatment period. In the CREDENCE trial, canagliflozin had a similar effect on the glomerular filtration rate with the curves crossing at approximately one year. The effect on proteinuria, on the other hand, was substantial, occurred soon after the start of treatment, and was sustained for the entire study period. In the randomized, double-blind DELIGHT trial, dapagliflozin reduced the urine albumin-to-creatinine ratio in type 2 diabetics with 21.0 % (95 % confidence interval -34.1 to -5.2; p=0.01) after 24 weeks of treatment. The effect was almost immediate and was sustained from 4-24 weeks.
Several facts suggest that the cardioprotective and renoprotective effects of SGLT-2 inhibitors are to some extent independent of their glucose-lowering effect. First, the reductions in the levels of HbA1c in the EMPA-REG OUTCOMES and DECLARE TIMI 58 trials were modest compared with the pronounced effects on cardiovascular and renal outcomes. Second, the effect on renal outcomes seems to be independent of the effect on HbA1c. Third, the DAPA-HF trial in patients with and without diabetes recently demonstrated that the effect on cardiovascular outcomes was as large in non-diabetics as in patients with diabetes. Finally, in the DAPA-CKD trial, 4304 patients with a baseline eGFR between 25 and 75 ml/min/1.73m2 with or without diabetes were randomized to treatment with dapagliflozin 10 mg or placebo once daily. The primary endpoint was a sustained decline in eGFR ≥ 50 %, end-stage kidney disease, or renal or cardiovascular death. There was a substantial reduction in the hazard of reaching the primary endpoint in the dapagliflozin arm (hazard ratio 0.61, p < 0.001) irrespective of whether the patients had diabetes or not.
One of the major mechanisms of action of the SGLT-2 inhibitors is to decrease proximal tubular sodium and chloride reabsorption in the kidneys, leading to a reset of the tubuloglomerular feedback. This induces plasma volume contraction without activation of the sympathetic nerve system, decreases harmful glomerular hyper-filtration leading to better long-term renal preservation, and improves the diuretic and natriuretic responses to other diuretic agents. How this translates into a beneficial effect on the cardiovascular system is at present unclear. Heart transplant recipients have many common features with the heart failure population with metabolic disturbances, a propensity for coronary disease (allograft vasculopathy), and progressive nephropathy. Based on these premises, DAPARHT trial is designed to assess the hypothesis that treatment with dapagliflozin for one year ameliorates the decline in kidney function that often occurs in heart transplant recipients.
- Conditions
- Heart Transplant Failure, Kidney Failure
- Being tested
- Dapagliflozin 10 mg, Placebo
- Keywords
- Renal protection, Heart transplant, Dapagliflozin
- Medical subject headings
- Renal Insufficiency
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dapagliflozin 10 mgDrug
Also called Farxiga
Participants will be randomized in a 1:1 fashion to receive 10 mg of oral dapagliflozin
PlaceboDrug
Participants will be randomized in a 1:1 fashion to receive a matching placebo once daily for one year.
| Study group | Role | What they receive |
|---|---|---|
| Dapagliflozin | Active comparator | Participants will be randomized in a 1:1 fashion to receive 10 mg of oral dapagliflozin (tablet) once daily for one year. Receives: Drug: Dapagliflozin 10 mg |
| Placebo | Placebo comparator | Participants will be randomized in a 1:1 fashion to receive a matching tablet once daily for one year. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
The chronic slope of the eGFR
The primary endpoint will be the slope of the eGFR from 2 weeks to end-of-treatment (12 months), calculated as the difference in eGFR from two weeks to 12 months after start of the intervention.
Measured: From 2 weeks to end-of-treatment (12 months)
The change in eGFR from baseline
Endpoints in open-label follow-up phase:
The change in eGFR from baseline to 1 month after end-of-treatment, 37 months after start of the intervention
Measured: From 2 weeks to 1 month after end-of-treatment (37 months)
Secondary outcomes (3)
Body weight
Change in body weight 2. The change in the albumin / creatinine ratio in the urine from baseline to end-of-treatment in patients with a baseline ratio > 30 mg/g at baseline 3. The change in the blood level of glycated haemoglobin (HbA1c) in patients with diabetes mellitus
Measured: From 2 weeks to end-of-treatment (12 months)
Glycosylated hemoglobin (HbA1c)
Change in the blood level of HbA1c in patient with diabetes mellitus
Measured: From 2 weeks to end-of-treatment (12 months)
Proteinuria
Change in the albumin / creatinine ratio in the urine in patients with a baseline ratio > 30 mg/g
Measured: From 2 weeks to end-of-treatment (12 months)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Apr 2022
- Study start8 Jun 2022
- Primary completion30 Sep 2028 (estimated)
- Study completion30 Nov 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Heart Transplant FailureStudies of the same condition, open and under way.
- More trials run by Oslo University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- The DAPARHT trial is a randomised, controlled, double blind, parallel group trial with an open-label extension phase. The primary endpoint is the slope of the eGFR measured from 2 weeks after randomisation and start of treatment to 12 months after start of treatment. The trial subjects immediately continue into the open-label phase. In this phase, patients assigned to dapagliflozin continue treatment for another 24 months. The primary endpoint of the open-label extension is the baseline-adjusted eGFR measured one month after the end of treatment, 37 months after randomisation.
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 430 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Oslo University Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Erasmus Medical Center, Skane University Hospital, Aarhus University Hospital, Karolinska University Hospital, Sahlgrenska University Hospital
- Responsible party
- Principal investigator, Lars Gullestad, Oslo University Hospital
- Investigators
- Olivier Manintveld, MD, PhD, Principal investigator, Erasmus Medical CenterOscar Braun, MD, PhD, Principal investigator, Skane University HospitalIda H Löfman, MD, PhD, Principal investigator, Karolinska University HospitalKevin Damman, MD, PhD, Principal investigator, University Medical Center GroningenMariusz Szymanski, MD, PhD, Principal investigator, UMC Utrecht
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05321706
- Sponsor's protocol ID
- 2021-003175-34
- Acronym
- DAPARHT
- Status last verified
- Mar 2026
- First submitted
- 22 Mar 2022
- Last updated
- 1 Jul 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Holmen S, Manintveld O, Damman K, Braun O, Lofman IH, Szymanski M, Ravnestad H, Gude E, Bjorkelund E, Andreassen AK, Gullestad L, Broch K. DAPAgliflozin for renal protection in heart transplant recipients. Rationale and design of the randomized controlled DAPARHT trial. Am Heart J. 2026 Jan;291:128-135. doi: 10.1016/j.ahj.2025.08.010. Epub 2025 Aug 19.
PubMed 40840822Garcia-Cosio Carmena MD, Farrero M, Blasco Peiro MT, Crespo M, Delgado Jimenez J, Diaz Molina B, Fernandez Rivera C, Garrido Bravo IP, Lopez Jimenez V, Melilli E, Mirabet Perez S, Perez Tamajon ML, Rangel Sousa D, Rodrigo E, Cruzado JM, Hernandez Marrero D; Spanish Society of Transplantation, the Spanish Society of Nephrology, and the Spanish Society of Cardiology (SET-SEC-SEN). Management of Kidney Disease in Heart Transplant Patients: A National Delphi Survey-based Consensus Expert Paper. Transplantation. 2025 Sep 1;109(9):e431-e445. doi: 10.1097/TP.0000000000005302. Epub 2025 Feb 7.
PubMed 39928546
Study at a glance
From the registry record, last updated by the sponsor on 1 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- DAPARHT: DAPAgliflozin for Renal Protection in Heart Transplant Recipients
- ClinicalTrials.gov ID
- NCT05321706
- Acronym / sponsor ID
- DAPARHT / 2021-003175-34
- Conditions
- Heart Transplant Failure, Kidney Failure
- Keywords
- Renal protection, Heart transplant, Dapagliflozin
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 430 participants (estimated)
- Lead sponsor
- Oslo University HospitalUniversity, hospital or other
- Collaborators
- Erasmus Medical Center, Skane University Hospital, Aarhus University Hospital, Karolinska University Hospital, Sahlgrenska University Hospital
- Study start
- 8 Jun 2022 (actual)
- Primary completion
- 30 Sep 2028 (estimated)
- Study completion
- 30 Nov 2028 (estimated)
- First posted
- 11 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Kidney failure is common in heart transplant recipients and is a major cause of morbidity and mortality. Sodium-glucose transporter 2 (SGLT2) inhibitors were developed as antidiabetics but were subsequently shown to reduce the incidence of adverse cardiovascular outcomes and protect renal function in non-diabetics as well as diabetics. However, SGLT2 inhibitors have not been tested in clinical trials in heart transplant recipients. The DAPARHT trial is designed to assess the effect of the SGLT2 inhibitor dapagliflozin to prevent deteriorating renal function in heart transplant recipients. Secondary objectives are to assess the impact of treatment on i) weight, ii) glucose homeostasis, iii) proteinuria, iv) the number of rejections, and (v) safety and tolerability. As exploratory outcomes, the investigators will assess the effect of treatment on renal outcomes, clinical events (death, myocardial infarction, cerebral stroke, cancer, and end-stage renal disease), cardiac function, quality of life, and new-onset diabetes.
Detailed description
Heart transplant is the treatment of choice for selected patients with end-stage heart failure. Worldwide, approximately 5000 procedures are performed annually. Whereas the first successful heart transplant led to a mere 18 days' prolongation of the recipient's life, the median survival after transplantation is now more than 11 years. Important surgical advances, as well as optimal medical therapy, are responsible for this improvement, but reducing morbidity and mortality further is a significant challenge. Beyond the first year, outcomes have not improved over the last decades. An important reason for this is the considerable burden of long-term side effects induced by immunosuppressive therapy. Chronic renal failure occurs in approximately 11 % of heart transplant recipients during the first five years after transplant and is associated with a large increase in mortality. A major cause of renal injury is a calcineurin inhibitor (CNI)-related nephrotoxicity. Calcineurin inhibitors revolutionized transplant medicine when introduced in the early 1980'ies and remain the mainstay of immunosuppressive therapy after a heart transplant. However, the therapy is an important contributor to post-transplant nephropathy. Furthermore, CNIs seem to contribute to metabolic disturbances including diabetes mellitus, hypertension, and oxidative stress after a heart transplant.
The deterioration of renal function after a heart transplant appears to be linear. In a Swedish material, the average yearly drop in the estimated glomerular filtration rate (eGFR) was 2.2 ± 14.6 ml/min/1.73 m2. In the NOCTET trial, which comprised 282 Scandinavian heart and lung transplant recipients who were randomized to treatment with a CNI or low-dose CNI and everolimus 1-10 years after surgery, the measured glomerular filtration rate (GFR) declined 7.2 ml/min/1.73m2 during a mean follow up of 5.6 years (i.e. 1.3 ml/min/1.73m2 per year) independently of the time since transplantation and baseline GFR.
Proteinuria is an important determinant of ensuing renal failure. Approximately 25 % of patients listed for heart transplant have at least trace proteinuria. Of the investigators' maintenance heart transplant recipients, 18 % have manifest proteinuria defined as urine protein/creatinine ratio ≥ 30 mg/g. The median ratio is 49.5 mg/g (interquartile range 37-84), consistent with a daily loss of approximately 500 mg of protein in the urine.
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) inhibit glucose reuptake in the proximal tubules of the nephrons. They thereby cause loss of glucose in the urine and induce osmotic diuresis. SGLT2i have now been studied in several large placebo-controlled cardiovascular outcomes trials in patients with type 2 diabetes. These trials were performed to satisfy regulatory requirements, specifically to exclude the excess risk of cardiovascular death, myocardial infarction, or stroke, and to test for efficacy. Despite a modest reduction in glycated haemoglobin (HbA1c), all the trials so far have shown that SGLT2i robustly reduces the risk of hospitalization for heart failure and prevents the progression of kidney disease.
In the EMPA-REG OUTCOME trial, treatment with the SGLT-2 inhibitor empagliflozin resulted in a reduction of cardiovascular mortality of 38%. In addition, empagliflozin significantly reduced admissions for heart failure and the incidence of end-stage kidney disease. Among patients allocated to empagliflozin, the mean change in estimated GFR (eGFR) from baseline to follow-up after 3 years was 4.7 ml per minute per 1.73 m2 better than in patients allocated to placebo. However, immediately after starting the drug, the patients on active treatment experienced an apparent reduction in the eGFR. The curves did not cross until after the first year of treatment, where after a between-group difference was manifest in favor of empagliflozin. The event curves diverged right up to the end of the trial, and there was an additional increase in the difference in the eGFR between the active drug arm and the placebo arm after stopping the treatment, suggesting that while empagliflozin is indeed renoprotective in patients with type 2 diabetes, there is an on-treatment suppression of eGFR analogue to the effect produced by angiotensin-converting enzyme inhibitors/angiotensin II receptor antagonists.
The DECLARE-TIMI 58 trial showed that the SGLT-2 inhibitor dapagliflozin reduced the rate of cardiovascular death or hospitalization for heart failure in a manner consistent with the findings observed in the EMPA-REG trial. Dapagliflozin was also associated with a large reduction in the rate of progression to end-stage renal failure. In consistence with the data on empagliflozin, 6 months after randomization, the mean decrease in the estimated GFR was larger in the dapagliflozin group than in the placebo group. However, the mean change equalized by 2 years, and at 3 and 4 years the mean decrease in eGFR was less with dapagliflozin than with placebo. The absolute difference in eGFR was smaller than that observed in the EMPA-REG OUTCOMES trial; however, the inclusion criteria in the DECLARE-TIMI 58 trial ensured that most of the participants had normal kidney function at the start of the treatment period. In the CREDENCE trial, canagliflozin had a similar effect on the glomerular filtration rate with the curves crossing at approximately one year. The effect on proteinuria, on the other hand, was substantial, occurred soon after the start of treatment, and was sustained for the entire study period. In the randomized, double-blind DELIGHT trial, dapagliflozin reduced the urine albumin-to-creatinine ratio in type 2 diabetics with 21.0 % (95 % confidence interval -34.1 to -5.2; p=0.01) after 24 weeks of treatment. The effect was almost immediate and was sustained from 4-24 weeks.
Several facts suggest that the cardioprotective and renoprotective effects of SGLT-2 inhibitors are to some extent independent of their glucose-lowering effect. First, the reductions in the levels of HbA1c in the EMPA-REG OUTCOMES and DECLARE TIMI 58 trials were modest compared with the pronounced effects on cardiovascular and renal outcomes. Second, the effect on renal outcomes seems to be independent of the effect on HbA1c. Third, the DAPA-HF trial in patients with and without diabetes recently demonstrated that the effect on cardiovascular outcomes was as large in non-diabetics as in patients with diabetes. Finally, in the DAPA-CKD trial, 4304 patients with a baseline eGFR between 25 and 75 ml/min/1.73m2 with or without diabetes were randomized to treatment with dapagliflozin 10 mg or placebo once daily. The primary endpoint was a sustained decline in eGFR ≥ 50 %, end-stage kidney disease, or renal or cardiovascular death. There was a substantial reduction in the hazard of reaching the primary endpoint in the dapagliflozin arm (hazard ratio 0.61, p < 0.001) irrespective of whether the patients had diabetes or not.
One of the major mechanisms of action of the SGLT-2 inhibitors is to decrease proximal tubular sodium and chloride reabsorption in the kidneys, leading to a reset of the tubuloglomerular feedback. This induces plasma volume contraction without activation of the sympathetic nerve system, decreases harmful glomerular hyper-filtration leading to better long-term renal preservation, and improves the diuretic and natriuretic responses to other diuretic agents. How this translates into a beneficial effect on the cardiovascular system is at present unclear. Heart transplant recipients have many common features with the heart failure population with metabolic disturbances, a propensity for coronary disease (allograft vasculopathy), and progressive nephropathy. Based on these premises, DAPARHT trial is designed to assess the hypothesis that treatment with dapagliflozin for one year ameliorates the decline in kidney function that often occurs in heart transplant recipients.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 2
- Model description
- The DAPARHT trial is a randomised, controlled, double blind, parallel group trial with an open-label extension phase. The primary endpoint is the slope of the eGFR measured from 2 weeks after randomisation and start of treatment to 12 months after start of treatment. The trial subjects immediately continue into the open-label phase. In this phase, patients assigned to dapagliflozin continue treatment for another 24 months. The primary endpoint of the open-label extension is the baseline-adjusted eGFR measured one month after the end of treatment, 37 months after randomisation.
| Arm | Type | Receives |
|---|---|---|
| Dapagliflozin | Active comparator | Drug: Dapagliflozin 10 mgParticipants will be randomized in a 1:1 fashion to receive 10 mg of oral dapagliflozin (tablet) once daily for one year. |
| Placebo | Placebo comparator | Drug: PlaceboParticipants will be randomized in a 1:1 fashion to receive a matching tablet once daily for one year. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Heart transplant recipient ≥ 1 year after heart transplant.
- Age ≥ 18 years
Key exclusion criteria (11 listed)
- Contraindications to study medication.
- Estimated GFR < 25 ml/min/m2
- Type I diabetes
- Severe liver failure (Child-Pugh's score C)
- Life expectancy reduced to < 2 years as judged by the investigator
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dapagliflozin 10 mgAlso: FarxigaParticipants will be randomized in a 1:1 fashion to receive 10 mg of oral dapagliflozin | Drug | Dapagliflozin |
| PlaceboParticipants will be randomized in a 1:1 fashion to receive a matching placebo once daily for one year. | Drug | Placebo |
Primary outcome
The chronic slope of the eGFR
Time frame: From 2 weeks to end-of-treatment (12 months)
The primary endpoint will be the slope of the eGFR from 2 weeks to end-of-treatment (12 months), calculated as the difference in eGFR from two weeks to 12 months after start of the intervention.
The change in eGFR from baseline
Time frame: From 2 weeks to 1 month after end-of-treatment (37 months)
Endpoints in open-label follow-up phase: The change in eGFR from baseline to 1 month after end-of-treatment, 37 months after start of the intervention
3 secondary outcomes
Body weight
Time frame: From 2 weeks to end-of-treatment (12 months)
Glycosylated hemoglobin (HbA1c)
Time frame: From 2 weeks to end-of-treatment (12 months)
Proteinuria
Time frame: From 2 weeks to end-of-treatment (12 months)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Jul 2026.
- Derived from this study: PubMed 40840822Holmen S, Manintveld O, Damman K, Braun O, Lofman IH, Szymanski M, Ravnestad H, Gude E, Bjorkelund E, Andreassen AK, Gullestad L, Broch K. DAPAgliflozin for renal protection in heart transplant recipients. Rationale and design of the randomized controlled DAPARHT trial. Am Heart J. 2026 Jan;291:128-135. doi: 10.1016/j.ahj.2025.08.010. Epub 2025 Aug 19.
- Derived from this study: PubMed 39928546Garcia-Cosio Carmena MD, Farrero M, Blasco Peiro MT, Crespo M, Delgado Jimenez J, Diaz Molina B, Fernandez Rivera C, Garrido Bravo IP, Lopez Jimenez V, Melilli E, Mirabet Perez S, Perez Tamajon ML, Rangel Sousa D, Rodrigo E, Cruzado JM, Hernandez Marrero D; Spanish Society of Transplantation, the Spanish Society of Nephrology, and the Spanish Society of Cardiology (SET-SEC-SEN). Management of Kidney Disease in Heart Transplant Patients: A National Delphi Survey-based Consensus Expert Paper. Transplantation. 2025 Sep 1;109(9):e431-e445. doi: 10.1097/TP.0000000000005302. Epub 2025 Feb 7.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Olivier Manintveld, MD, PhD principal investigator
Erasmus Medical Center
Oscar Braun, MD, PhD principal investigator
Skane University Hospital
Ida H Löfman, MD, PhD principal investigator
Karolinska University Hospital
6 sites in 3 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Dapagliflozin 10 mg in people with Heart Transplant Failure and Kidney Failure, run by Oslo University Hospital at 6 sites in 3 countries.
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 11 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: under way, not looking for participants, as of the sponsor's last update on 1 Jul 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 Netherlands, Sweden, Norway. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The chronic slope of the eGFR (time frame: From 2 weeks to end-of-treatment (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?
On the ClinicalTrials.gov record for NCT05321706, which also lists 2 linked publications.
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 1 Jul 2026.