The RENAL LIFECYCLE Trial: A RCT to Assess the Effect of Dapagliflozin on Renal and Cardiovascular Outcomes in Patients With Severe CKD
- Conditions
- Kidney Disease, ChronicRenal Transplant FailureHeart FailureKidney FailureDeath
- Interventions
- Drug: Placebo
- Registration Number
- NCT05374291
- Lead Sponsor
- University Medical Center Groningen
- Brief Summary
Rationale:
Sodium glucose co transporter 2 (SGLT2) inhibitors are a relatively new class of agents, originally developed as oral antihyperglycemic drugs. SGLT2 inhibitors are clinically available since 2012 for the treatment of patients with diabetes mellitus type 2. Later, SGLT2 inhibitors appeared to have also specific reno- and cardioprotective effects. Remarkably, the trials that have been performed thus far excluded patients with an eGFR below 25 mL/min/1.73m2 at inclusion, prevalent dialysis patients, and kidney transplant recipients. This is unfortunate, because especially these patients are at high risk of reaching kidney failure requiring dialysis, cardiovascular complications and mortality, whereas there are only few proven effective therapies. There is emerging evidence from experimental studies and post hoc-analyses of randomized clinical trials that SGLT2 inhibitors may also be effective in preventing cardiovascular and mortality outcomes in these patients with severe CKD, including patients receiving dialysis or living with a kidney transplant. For instance, subgroup analysis of the DAPA-CKD trial comparing 624 patients with an eGFR\<30 to the remainder of the trial population with better kidney function, demonstrated that the efficacy of the SGLT2 inhibitor dapagliflozin in reducing cardiovascular, heart failure and renal outcomes persisted in the population with impaired kidney function. Furthermore, in the DAPA-CKD trial patients continued to use dapagliflozin or placebo when dialysis was initiated. In the subgroup of patients who initiated dialysis, dapagliflozin was associated with a relative risk reduction for mortality of 21%. Finally, in kidney transplant recipients, SGLT2 inhibitors have been shown to be effective in lowering HbA1c, body weight, blood pressure and stabilize kidney function, and these agents were well tolerated and safe. Taken these findings together there is a sound rationale to study the long-term reno- and cardioprotective efficacy and safety of SGLT2 inhibitors in patients with severe CKD.
There are two cardiac sub-studies: the cardiac MRI substudy and the echocardiography sub-study.
The echocardiography sub-study is referred to as the "SGLT-2-inhibitors to Target Heart Failure in Peritoneal Dialysis" (STOP HF in PD) study. In STOP HF in PD the effect of dapagliflozin on cardiac function will be assessed in a subset of 100 patients treated with peritoneal dialysis.
- Detailed Description
Objective:
To establish the reno- and cardioprotective efficacy and safety of dapagliflozin in patients with severe CKD
Study design:
Multicenter, randomized, controlled, double blinded, pragmatic, interventional trial
Study population:
* Patients with advanced CKD, i.e. an eGFR ≤25 mL/min\*1.73m2
* Patients on dialysis (at least 3 months after start of dialysis)
* Patients with a kidney transplant and an eGFR ≤45 mL/min/1.73m2 (at least 6 months after transplantation)
Intervention:
Dapagliflozin 10 mg/day or matching placebo
Primary outcome measure:
Combined endpoint of all-cause mortality, kidney failure, and hospitalization for heart failure in the overall study population
Study duration:
18 month recruitment phase, 30 month follow-up after enrollment of the last patient: Total study duration intended to last 48 months. It should be noted that the trial is event driven and will be terminated when 468 primary composite outcomes have occurred. The exact trial duration may therefore be shorter or longer than the intended 48 months.
Study visits:
Screening, baseline, week 2, month 3, month 6 and every 6 months thereafter. Information needed for the trial will be obtained as much as possible from visits taking place as part of routine clinical care.
Sample size:
Renal Lifecycle is designed as an endpoint driven trial and will finish when 468 primary study outcomes have occurred. The investigators have estimated a sample size of 1500 patients.
Novel aspects:
A unique patient population with severe chronic kidney disease at very high risk of adverse outcomes for whom very few proven effective therapies exist. The initiation and efficacy of SGLT2 inhibitors, including dapagliflozin, has not been studied before in this population. However, SGLT2 inhibitors have the potential to be very effective and well tolerated which would imply a major advance in the pharmacotherapy of these patients.
When patients reach a renal endpoint, e.g. start or chronic dialysis or receiving a kidney transplantation, study medication will not be stopped as customary in many other trials in nephrology, but continued in the new phase of their "renal lifecycle", hence the name of the trial.
Sub studies:
Cardiac sub-studies The cardiac MRI sub-study will evaluate the effect of dapagliflozin, as compared to placebo, on left ventricular mass, an intermediate cardiovascular outcome, in 250 participants with advanced CKD. This will provide robust evidence on the mechanisms under-pinning the cardioprotective effects of SGLT2 inhibitors in this high-risk patient population. The cardiac echocardiography sub-study will evaluate the effect of dapagliflozin, as compared to placebo, on LV-GLS, in 100 participants with ESKD treated with peritoneal dialysis. This will provide additional evidence on the mechanisms underlying the cardio-protective effects of SGLT2i in patients with ESKD. Furthermore, the GLS-data will be related to measured CKD- and PD-associated mediators of heart failure (measured in serum, urine and peritoneal effluent. This will aid to determine their relevance in patients with ESKD, as well as to define if and to what extent SGLT2i affect these mediators in patients with ESKD. Finally, this sub-study allows prospective evaluation of LV-GLS as a predictor of adverse cardiovascular events in patients treated with PD.
Cognitive sub-study Patients with chronic kidney disease (CKD) are at a much higher risk for developing cognitive impairment compared with the general population and both lower glomerular filtration rate and the presence of albuminuria are associated with its development. SGLT-2 inhibitor use is associated with better preservation of cognitive function in patients with CKD including those on hemodialysis and after kidney transplantation compared to placebo.Patients will be requested to perform the symbol digit modalities test at the same time as the questionnaires, i.e. at baseline (visit 2), visit 5 and visit 6, once every year after visit 6 and at EoT/EET.The primary outcome of the cognition sub study is the change over time in the number of correct answers in the symbol digit modalities test within 90 seconds.
kidney metabolism substudy The primary aim of this substudy is to evaluate the effect of dapagliflozin 10 mg compared to a placebo on energy metabolism assessed by changes in the renal mitochondrial oxidative phosphorylation capacity in kidney transplant recipients participating in the RENAL LIFECYCLE Trial at the 3-month Follow-up Visit. Further aims of this substudy are to evaluate the differences in metabolic substrate preferences by measuring ketone body or acylcarnitine substrate-driven mitochondrial respiration following the randomization to dapagliflozin or placebo.
Differences in mitochondrial architecture including mitochondrial quantity and morphology will be assessed using electron microscopy.
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 1500
- Patients with advanced CKD i.e. an eGFR ≤25 mL/min/1.73m2
- Dialysis patients (at least 3 months after start of dialysis)
- Transplant patients with an eGFR ≤45 mL/min/1.73m2 (at least 6 months after transplantation)
In addition, to be eligible all subjects must meet all criteria below
- Age >18 years
- Willing to sign informed consent
- Pre-dialysis patients with eGFR ≤25 mL/min/1.73m2 have to be on a stable dose (no changes in dose or type of drug) of ACEis or ARBs for at least 4 weeks prior to the screening visit to be eligible to proceed to the randomization visit unless there is documented evidence that the patient does not tolerate an ACEi or ARB. These subjects will maintain their stable doses of ACEis or ARBs throughout the trial (when possible and tolerated by the patient). ACEi or ARBs are not required for patients on maintenance dialysis or kidney transplant recipients.
- Mentally incapacitated subjects (i.e. not able to sign informed consent)
- Diagnosis of type 1 diabetes mellitus
- Concurrent treatment with SGLT2 inhibitor
- History of ≥2 urinary tract / genital infections during the last six months
- Life expectancy <6 months in the opinion of the treating physician.
- Scheduled start of dialysis within 3 months or kidney transplantation within 6 months
- patients treated for a renal indication during the last 6 months with a course of systemic immunosuppressive agents or intensification of treatment with systemic immunosuppressive agents, such as patients with a kidney transplant and acute rejection or patients with GPA (Morbus Wegener) and a recent flare.
- Active malignancy aside from treated squamous cell or basal cell carcinoma of the skin.
- History of severe hypersensitivity or known severe hepatic impairment (Child-Pugh class C)
- History of severe noncompliance to medical regimens or unwillingness to comply with the study protocol.
- Pregnancy or breastfeeding
- Presence of other transplanted organ besides a kidney transplant
- Severe lactose intolerance
- Autosomal Dominant Polycystic Kidney Disease (ADPKD) treated with tolvaptan
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo Placebo 10 mg/day (oral) Dapagliflozin Dapagliflozin 10 mg/day (oral) Dapagliflozin 10 mg/day (oral)
- Primary Outcome Measures
Name Time Method Number of partipants with all-cause mortality, kidney failure, and hospitalization for heart failure Total study duration intended to last 48 months To determine whether dapagliflozin is superior to placebo in reducing the incidence of the primary composite endpoint
Combined endpoint of all-cause mortality, kidney failure, and hospitalization for heart failure in the overall study population
- Secondary Outcome Measures
Name Time Method Number of participants to reach all-cause mortality Total study duration intended to last 48 months To determine if dapagliflozin is superior to placebo in reducing the incidence of all-cause mortality
Incidence of hospitalization for heart failure Total study duration intended to last 48 months Incidence of hospitalization for heart failureTo determine if dapagliflozin is superior to placebo in reducing the incidence of heart failure
Incidence of kidney failure (chronic dialysis, kidney transplantation or mortality due to kidney failure) Total study duration intended to last 48 months To determine if dapagliflozin is superior to placebo in reducing the incidence of kidney failure
incidence of the composite outcome (kidney failure, hospitalization for heart failure, and all-cause mortality) in subgroups Total study duration intended to last 48 months To determine whether dapagliflozin is superior to placebo in reducing the incidence of the composite outcome in subgroups
subgroups: advanced CKD i.e. an eGFR ≤30 mL/min/1.73m2, dialysis patients and transplant patients
Trial Locations
- Locations (65)
Deventer Ziekenhuis
🇳🇱Deventer, Netherlands
Dialysecentrum Tergooi
🇳🇱Hilversum, Netherlands
St. Jansdal ziekenhuis
🇳🇱Lelystad, Netherlands
Wollongong Hospital
🇦🇺Wollongong, New South Wales, Australia
Sunshine Coast Hospital and Health Services
🇦🇺Birtinya, Queensland, Australia
Royal Brisbane and Womens Hospital
🇦🇺Brisbane, Queensland, Australia
Liverpool Hospital
🇦🇺Sydney, New South Wales, Australia
Townsville University hospital
🇦🇺Douglas, Queensland, Australia
Charité
🇩🇪Berlin, Germany
St George Hospital
🇦🇺Sydney, New South Wales, Australia
Royal Melbourne Hospital
🇦🇺Parkville, Victoria, Australia
Universitätsklinikum Halle (Saale) Innere Medizin 2
🇩🇪Halle, Germany
Royal Adelaide Hospital
🇦🇺Adelaide, South Australia, Australia
Royal Prince Alfred Hospital
🇦🇺Sydney, New South Wales, Australia
Nierenzentrum Heidelberg
🇩🇪Heidelberg, Germany
Universitätsklinikum Tübingen Medizinische Klinik IV
🇩🇪Tübingen, Germany
Dialysecentrum Dianet (Amsterdam)
🇳🇱Amsterdam, Netherlands
Zentrum fuer Nieren-, Hochdruck- und Stoffwechselerkrankungen Hannover
🇩🇪Hannover, Germany
East Metro Health Services (Royal Perth Hospital and Armadale Health Services)
🇦🇺Perth, Western Australia, Australia
Canberra Health Services
🇦🇺Canberra, Australian Capital Teritory, Australia
Concord Repatriation General Hospital
🇦🇺Sydney, New South Wales, Australia
Western Health
🇦🇺Melbourne, Victoria, Australia
Box Hill Hospital (Eastern Health)
🇦🇺Melbourne, Australia
Praxis für Dialyse und Nierenkrankheiten
🇩🇪Berlin, Germany
Universitätsklinikum Erlangen
🇩🇪Erlangen, Germany
Universitätsklinikum Düsseldorf
🇩🇪Düsseldorf, Germany
Universitätsklinikum JenaKlinik für Innere Medizin III
🇩🇪Jena, Germany
Dialysezentrum Heilbronn - Überörtliche Berufsausübungsgemeinschaft für Nephro und Dialyse (ÜBAG)
🇩🇪Heilbronn, Germany
Universitätsklinikum RegensburgAbteilung für Nephrologie
🇩🇪Regensburg, Germany
Universitätsmedizin Mainz
🇩🇪Mainz, Germany
Universitätsklinikum Ulm, Klinik für Innere Medizin I, Nephrologie
🇩🇪Ulm, Germany
Nephrologisches Zentrum Villingen/Schwenningen
🇩🇪Villingen-Schwenningen, Germany
Nierenzentrum Wiesbaden
🇩🇪Wiesbaden, Germany
Medizinische Klinik und Poliklinik I der Universitätsklinik WürzburgSchwerpunkt Nephrologie
🇩🇪Würzburg, Germany
Amsterdam UMC
🇳🇱Amsterdam, Noord-Holland, Netherlands
Amphia Ziekenhuis
🇳🇱Breda, Noord-brabant, Netherlands
Noordwest Ziekenhuisgroep Alkmaar
🇳🇱Alkmaar, Netherlands
Meander Medisch Centrum
🇳🇱Amersfoort, Netherlands
Gelre Ziekenhuizen
🇳🇱Apeldoorn, Netherlands
Albert Schweitzer ziekenhuis
🇳🇱Dordrecht, Zuid-Holland, Netherlands
Niercentrum aan de Amstel
🇳🇱Amstelveen, Netherlands
Reinier de Graaf Ziekenhuis
🇳🇱Delft, Netherlands
Jeroen Bosch Ziekenhuis
🇳🇱Den Bosch, Netherlands
Catharina Ziekenhuis Eindhoven
🇳🇱Eindhoven, Netherlands
Franciscus Gasthuis en Vlietland
🇳🇱Rotterdam, Netherlands
Maxima Medisch Centrum
🇳🇱Eindhoven, Netherlands
Elyse klinieken voor nierzorg
🇳🇱Kerkrade, Netherlands
Martini Ziekenhuis
🇳🇱Groningen, Netherlands
UMCG
🇳🇱Groningen, Netherlands
Bernhoven
🇳🇱Uden, Netherlands
Spaarne Gasthuis
🇳🇱Hoofddorp, Netherlands
Medisch Centrum Leeuwarden
🇳🇱Leeuwarden, Netherlands
Leiden UMC
🇳🇱Leiden, Netherlands
Maastricht UMC+
🇳🇱Maastricht, Netherlands
Radboud UMC
🇳🇱Nijmegen, Netherlands
St. Antonius Ziekenhuis
🇳🇱Nieuwegein, Netherlands
Bravis ziekenhuis
🇳🇱Roosendaal, Netherlands
Diakonessenhuis Utrecht
🇳🇱Utrecht, Netherlands
Dialysecentrum Dianet (Utrecht)
🇳🇱Utrecht, Netherlands
VieCuri Medisch Centrum
🇳🇱Venlo, Netherlands
UMC Utrecht
🇳🇱Utrecht, Netherlands
Isala Ziekenhuis
🇳🇱Zwolle, Netherlands
Westmead Hospital
🇦🇺Sydney, New South Wales, Australia
Royal North Shore Hospital
🇦🇺Sydney, New South Wales, Australia
Prince of Wales Hospital
🇦🇺Sydney, New South Wales, Australia