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- Sperimentazione clinica NCT07682350
SGLT2i Effect on PTDM Development and Kidney Allograft Function in Non-diabetic Kidney Transplant Recipients: A Randomized, Doubleblind, Placebo Controlled, National Multicenter Trial (SGL-TX-PTDM)
SGL-TX-PTDM: SGLT2i Effect on PTDM Development and Kidney Allograft Function in Kidney Transplant Recipients: A Randomized, Doubleblind, Placebo Controlled, National Multicenter Trial
The goal of this clinical trial is to find out whether 12 months of treatment with the SGLT2 inhibitor Forxiga® (dapagliflozin 10 mg once daily), compared with placebo, can reduce the risk of developing post-transplant diabetes in kidney transplant recipients who do not have diabetes at the time of transplantation.
The main questions it aims to answer are:
- Does Forxiga reduce the risk of developing post-transplant diabetes and prediabetes compared with placebo?
- Does Forxiga help preserve the function of the transplanted kidney compared with placebo?
- Is Forxiga safe for kidney transplant recipients who do not have diabetes?
- Does Forxiga affect the occurrence of urinary tract infections, the amount of protein in the urine, and other kidney- and heart-related health measures compared with placebo?
Researchers will compare Forxiga with a placebo (a look-alike tablet containing no active medicine) to see whether it can reduce the risk of post-transplant diabetes while maintaining kidney function and remaining safe to use.
Adults who have recently received a kidney transplant and do not have diabetes may take part if they meet the study requirements.
Participants will be randomly assigned to receive either Forxiga or placebo once daily for 12 months. They will attend study visits 3, 6, and 12 months after joining the study. These visits will include health checks, blood tests, and urine tests. Neither the participants nor the study doctors will know which treatment each participant is receiving.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Background Kidney transplantation is the best treatment of end-stage renal disease (ESRD), although median allograft survival is only 15 years. In non-transplant patients with chronic kidney disease (CKD) sodium-glucose co-transporter type 2 inhibitors (SGLT2i) protects kidney function and reduces decline in estimated glomerular filtration (eGFR) and in KTR with PTDM, SGLT2i improve glucose regulation.
Perspective With the current kidney transplant survival of average 15 years, app. one out of ten adult[1] kidney transplant recipients (KTR) outlive their donated kidneys. This poses a significant burden to the patients and society and increases the demand for new transplantations. WHO reported a 9% increase in the number of kidney transplant recipients from 2022 to 2023[2]. The growing population of kidney transplant recipients underscores the importance of research aimed at prolonging graft survival and preventing post-transplant diabetes mellitus (PTDM). The efficacy of SGLT2i on reducing PTDM incidence remain untested in KTR.
The SGL-TX-PTDM study aim to investigate the effect of SGLT2i on the incidence of PTDM. PTDM is associated with a 63% increased risk for graft failure and an 87% increased risk for death[8]. PTDM is therefore known to be a threat to graft and patient survival throughout many years [9]. In the long-term perspective, we hope to contribute with knowledge to preserve kidney transplant function, benefit society, and improve patients' quality of life.
Hypothesis We hypothesize that SGLT2i will reduce the incidence of PTDM in non-diabetic KTR as an add-on to standard-of-care.
Research Objective In this superior randomized controlled clinical trial we will determine the effect of oral SGLT2i compared with placebo as add-on to standard-of-care on incidence of PTDM in non-diabetic KTR.
The secondary objectives will evaluate the effect of oral SGLT2i on prediabetes status, eGFR, U-ACR, urinary tract infection, renal parameters, cardiovascular parameters and adverse events in non-diabetic KTR.
Design An investigator-initiated, placebo-controlled, double-blinded, parallel-group, randomized, national, multicenter intervention study.
Methods Adults without pre-existing diabetes who are admitted for kidney transplantation will be screened for eligibility and invited to participate. Written informed consent will be obtained prior to any study-specific procedures. When the kidney allograft achieves an estimated glomerular filtration rate (eGFR) of 25 mL/min, eligible participants will be randomized in a 1:1 allocation ratio to receive either 12 months of oral SGLT2 inhibitor therapy (Dapagliflozin 10 mg once daily) or a matching placebo. Study medication will be administered in addition to standard immunosuppressive therapy.
Participants will continue to receive routine post-transplant clinical care throughout the study period. Study assessments will be conducted at baseline and at 3, 6, and 12 months following randomization. Clinical evaluations will include blood and urine laboratory tests, with safety and efficacy monitored at each visit by the treating nephrologist.
Post-transplant diabetes mellitus (PTDM) will be assessed according to the diagnostic criteria of the American Diabetes Association (ADA). All study procedures, data collection time points, and outcome assessments follow the SPIRIT 2025 guidance for interventional trial protocols.
Primary endpoint
• PTDM incidence after 3, 6 and 12 month follow up. , defined as any of the following criteria (HbA1c ≥ 48 mmol/mol or Fasting plasma glucose ≥ 7.0 mmol/L or random plasma glucose ≥ 11.1 mmol/L)
Secondary endpoint
Prediabetes status after 3,6 and 12 month follow up, defined as any of the following criteria (HbA1c between 39-47 mmol/mol or Impaired fasting plasma glucose between 5.6-6.9 mmol/L or Continuous glucose monitoring mean blood glucose time above range 7,8 mmol/L
▪ Kidney allograft function (eGFR) change after 3, 6 and 12 month follow up.
- Albumin/creatinine ratio (U-ACR) (mg/g), after 3, 6 and 12 month follow up.
- Blood samples after 3, 6 and 12 month follow up. (Creatinine (umol/L, Total-Cholesterol, Low-and high-density lipoproteins (LDL and HDL, respectively) and triglycerides, Clinical routine Tacrolimus concentration (ug/L))
- Urinary tract infection (positive culture) incidence after 3, 6 and 12 month follow up.
- Incidence of kidney transplant rejection (biopsy verified) after 3, 6 and 12 month follow up.
- Renal composite outcome after 3, 6 and 12 month follow up. (Incidence of graft failure - defined as return to dialysis or retransplantation or Incidence of ESRD (defined as eGFR<15 ml/min/1.73m2) or Incidence of > 25% increase in creatinine
- Change in Systolic blood pressure (SysBP) (mmHg) and diastolic blood pressure (DiaBP) (mmHg), after 3, 6 and 12 month follow up.
- Relative incidence of out-of-target measures of clinical routine blood Tacrolimus levels
- Urine biomarkers indicative of podocyt and tubular function from selected sites
- Incidence of: Adverse events, Serious adverse events, Serious adverse reactions, Death - all cause mortality, and Major Adverse Cardiac Events (MACE)
Tertiary endpoints
• SF-36 (Short Form Health Survey 36)
Study population A total of 184 adults without pre-existing diabetes who undergo kidney transplantation will be recruited from three Danish transplant centers: Odense University Hospital (OUH), Aarhus University Hospital (AUH), and Copenhagen University Hospital - Rigshospitalet (RH). Participants will be enrolled once the kidney allograft has achieved an estimated glomerular filtration rate (eGFR) ≥ 25 mL/min. Eligible participants will then be randomized to receive either a daily dose of SGLT2 inhibitor or matching placebo for 12 months following randomization.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Lotte B Lange, MD
- Numero di telefono: +45 40863392
- Email: Lotte.Borg.Lange@rsyd.dk
Luoghi di studio
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Aarhus, Danimarca, 8200
- Department of Renal Medicine
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Contatto:
- Henrik Birn, Head of research
- Numero di telefono: +45 40460831
- Email: hb@clin.au.dk
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Copenhagen, Danimarca, 2100
- Department of Nephrology and Endocrinology.
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Contatto:
- Mads Hornum, Head of research
- Numero di telefono: +45 35459608
- Email: Mads.Hornum@regionh.dk
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Odense, Danimarca, 5000
- Department of Nephrology, Odense University Hospital
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Contatto:
- Lotte B Lange, MD
- Numero di telefono: +45 40863392
- Email: Lotte.Borg.Lange@rsyd.dk
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Obtained written informed consent
- Male or female patients, age ≥ 18 years.
- Non-diabetic KTR
- Immunosuppressive must include Tacrolimus
Exclusion Criteria:
- Patients who is treated (diet or antidiabetics) for diabetes type 1 or 2 before randomization
- eGFR< 25 ml/min/1.73m2 (before randomization)
- Alanine aminotransferase (ALAT) > 3 x upper normal limit
- Bilirubin > 2 x upper normal limit
- Pregnancy
- Positive plasma hCG
- Breastfeeding
- Known allergy towards SGLT2i or the content substance
- Patients with chronic intestinal diseases, including inflammatory bowel diseases (e.g., Crohn's disease and ulcerative colitis) and structural conditions such as short bowel syndrome.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Comparatore attivo: Sglt2i
Dose giornaliera di SGLT2I (tavoletta forxiga da 10 mg)
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The intervention in this clinical trial will be treatment with an SGLT2 inhibitor (Forxiga, 10 mg tablet once daily) compared with a matching placebo.
A total of 184 non-diabetic kidney transplant recipients will be enrolled.
All participants will be randomized in a 1:1 ratio to receive either Forxiga or placebo as an add on to standard immunosuppressive therapy.
This intervention differs from other studies by specifically targeting non-diabetic kidney transplant recipients, a population in which the efficacy and safety of SGLT2 inhibitors have not yet been established.
Altri nomi:
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Comparatore placebo: Placebo
Dose giornaliera di tablet placebo
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The control intervention in this clinical trial will be a matching placebo tablet, identical in appearance to Forxiga (10 mg), administered once daily as an add on to standard immunosuppressive therapy.
A total of 184 non-diabetic kidney transplant recipients will be enrolled.
All participants will be randomized in a 1:1 ratio to receive either placebo or Forxiga.
This placebo intervention ensures blinding of both participants and investigators and allows a direct comparison of the safety and efficacy of SGLT2 inhibition versus no active treatment in this unique patient population.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence of post-transplant diabetes mellitus (PTDM)
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Post-transplant diabetes mellitus Specific measurement: Diagnosis of PTDM according to the American Diabetes Association (ADA) diagnostic criteria. Specific metric: Number of participants with PTDM Method of aggregation: Proportion of participants with PTDM in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Prediabetes status
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Prediabetes Specific measurement: Prediabetes defined as HbA1c 39-47 mmol/mol, impaired fasting plasma glucose 5.6-6.9 mmol/L. Specific metric: Number of participants with prediabetes Method of aggregation: Proportion of participants with prediabetes in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Change in kidney allograft function
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Kidney allograft function Specific measurement: Estimated glomerular filtration rate (eGFR), calculated using the CKD-EPI equation (mL/min/1.73 m²). Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Change in proteinuria
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Proteinuria Specific measurement: Urine albumin-to-creatinine ratio (U-ACR), expressed as mg/g. Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Change in biochemical parameters
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Biochemical parameters Specific measurement: Serum creatinine (µmol/L), total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglycerides, and tacrolimus trough concentration (µg/L). Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Urinary tract infections
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Urinary tract infections Specific measurement: Positive urine cultures confirming urinary tract infection. Specific metric: Total number of urinary tract infection episodes Method of aggregation: Total number of urinary tract infection episodes in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Kidney transplant rejection
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Kidney transplant rejection Specific measurement: Biopsy-verified kidney transplant rejection.
Specific metric: Number of participants with at least one biopsy-verified kidney transplant rejection episode Method of aggregation: Proportion of participants with at least one biopsy-verified rejection episode in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization
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Follow up at 3,6 and 12 months after randomization
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Renal composite outcome
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Renal composite outcome Specific measurement: Occurrence of any of the following: graft failure (defined as return to dialysis or kidney retransplantation), end-stage kidney disease (defined as eGFR <15 mL/min/1.73 m²), or a >25% increase in serum creatinine from baseline. Specific metric: Number of participants experiencing the renal composite outcome Method of aggregation: Proportion of participants experiencing the renal composite outcome in each treatment group (dapagliflozin versus placebo) Time point: 3, 6, and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Change in blood pressure
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Blood pressure Specific measurement: Systolic blood pressure and diastolic blood pressure, measured in mmHg. Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: 3, 6 and 12 months after randomization |
Follow up at 3,6 and 12 months after randomization
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Out-of-target tacrolimus trough concentrations
Lasso di tempo: Follow up at 3,6 and 12 months after randomization
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Domain: Tacrolimus trough concentrations Specific measurement: Clinical routine tacrolimus trough concentration >6 µg/L.
Specific metric: Number of participants with at least one out-of-target tacrolimus trough concentration Method of aggregation: Proportion of participants with at least one out-of-target tacrolimus trough concentration in each treatment group (dapagliflozin versus placebo) Time point: 3, 6, and 12 months after randomization
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Follow up at 3,6 and 12 months after randomization
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Change in urinary biomarkers indicative of podocyte and tubular function
Lasso di tempo: Baseline and 6 months follow up
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Domain: Urinary biomarkers of podocyte and tubular function Specific measurement: Urinary biomarkers indicative of podocyte and tubular function (e.g., NGAL and KIM-1) measured in participants from selected study sites. Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: Baseline and 6 months after randomization |
Baseline and 6 months follow up
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Incidence of adverse events, serious adverse events, serious adverse reactions, all-cause mortality, and major adverse cardiovascular events (MACE)
Lasso di tempo: Follow up at 12 months after randomization
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Domain: Safety Specific measurement: Incidence of adverse events (AEs), serious adverse events (SAEs), serious adverse reactions (SARs), all-cause mortality, and major adverse cardiovascular events (MACE). Specific metric: Number of participants experiencing one or more safety events Method of aggregation: Proportion of participants experiencing one or more safety events in each treatment group (dapagliflozin versus placebo) Time point: 12 months after randomization |
Follow up at 12 months after randomization
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Health-related quality of life
Lasso di tempo: By baseline and 12 months after randomization
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Domain: Health-related quality of life Specific measurement: Short Form Health Survey 36 (SF-36) Physical Component Summary (PCS) and Mental Component Summary (MCS) scores. Specific metric: Change from baseline Method of aggregation: Mean change from baseline in each treatment group (dapagliflozin versus placebo) Time point: Baseline and 12 months after randomization |
By baseline and 12 months after randomization
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Lotte B Lange, MD, Department of Nephrology, Odense University Hospital
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- EU CT:2024-518774-14-00
- 2024-518774-14-00 (Ctis)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Data Available:
Individual participant data (IPD) that underlie the results reported in the published article will be shared after de-identification. This includes text, tables, figures, and appendices.
Supporting Documents:
The study protocol and statistical analysis plan will also be made available.
Time Frame:
Data will be shared immediately following publication. There is no specified end date for availability.
Criteria for Access:
Data will be shared with researchers who submit a methodologically sound proposal aimed at achieving the goals outlined in their approved research proposal.
Access Mechanism:
Interested researchers should direct their proposals to:
lotte.borg.lange@rsyd.dk. To gain access, requestors will be required to sign a data access agreement.
Data Storage:
The data will be stored for 25 years on a secure third-party platform (OPEN).
Periodo di condivisione IPD
The data will be available after the last patients last visit.
Data Storage:
The data will be stored for 25 years on a secure third-party platform (OPEN).
Criteri di accesso alla condivisione IPD
Criteria for Access:
Data will be shared with researchers who submit a methodologically sound proposal aimed at achieving the goals outlined in their approved research proposal.
Interested researchers should direct their proposals to:
lotte.borg.lange@rsyd.dk. To gain access, requestors will be required to sign a data access agreement.
Tipo di informazioni di supporto alla condivisione IPD
- STUDIO_PROTOCOLLO
- LINFA
- RSI
Informazioni su farmaci e dispositivi, documenti di studio
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