FIDELIO-DKDFinerénone et soins standard pour retarder la progression de la maladie rénale dans le diabète de type 2
Cette étude vise à évaluer l'efficacité du Finerénone, en association avec les soins standard, dans le ralentissement de la progression de la maladie rénale chez les individus atteints de diabète de type 2, en observant la première occurrence d'une insuffisance rénale, d'une diminution soutenue de la fonction rénale, ou d'un décès rénal.
Finerenone (BAY94-8862)
+ Placebo
Maladies génito-urinaires+17
+ Maladie chronique
+ Diabète Mellitus
Étude thérapeutique
Résumé
Date de début de l'étude : 17 septembre 2015
Date à laquelle le premier participant a commencé l'étude.This study focuses on individuals with Type 2 Diabetes Mellitus who also have a clinical diagnosis of Diabetic Kidney Disease. The main goal is to test if a drug called Finerenone, when used alongside standard care, is more effective than a placebo in slowing down the progression of kidney disease. This research is important as it could potentially improve the care and treatment for those living with this condition, addressing a significant health challenge and unmet need. In this study, participants are randomly assigned to receive either Finerenone or a placebo, neither the participants nor the researchers know who is receiving which. The effectiveness of the drug is measured by observing the time it takes for the first occurrence of kidney failure, a sustained decrease in the estimated glomerular filtration rate (eGFR) by 40% or more from the baseline over at least 4 weeks, or renal death. The results are evaluated by counting the number of participants who experience these outcomes and calculating the hazard ratio, which helps to understand the risk reduction associated with Finerenone treatment.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.5734 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 18 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria: * Men or women ≥18 years of age * Type 2 diabetes mellitus (T2D) as defined by the American Diabetes Association * Diagnosis of chronic kidney disease (CKD) with at least one of the following criteria at run-in and screening visits: * persistent high albuminuria (UACR ≥30 to \<300 mg/g in 2 out of 3 first morning void samples) and estimated glomerular filtration rate (eGFR) ≥25 but \<60 mL/min/1.73 m² (CKD EPI) and presence of diabetic retinopathy or * persistent very high albuminuria (UACR ≥300 mg/g in 2 out of 3 first morning void samples) and eGFR ≥25 to \<75 mL/min/1.73 m² (CKD-EPI) * Prior treatment with angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) as follows: * For at least 4 weeks prior to the run-in visit, subjects should be treated with either an ACEI or ARB, or both * Starting with the run-in visit, subjects should be treated with only an ACEI or ARB * For at least 4 weeks prior to the screening visit, subjects should be treated with the maximum tolerated labeled dose (but not below the minimal labeled dose) of only an ACEI or an ARB (not both) preferably without any adjustments to dose or choice of agent or to any other antihypertensive or antiglycemic treatment * Serum potassium ≤4.8 mmol/L at both the run-in and the screening visit Exclusion Criteria: * Known significant non-diabetic renal disease, including clinically relevant renal artery stenosis * Uncontrolled arterial hypertension (ie, mean sitting systolic blood pressure (SBP) ≥170 mmHg, sitting diastolic blood pressure (DBP) ≥110 mmHg at run-in visit, or mean sitting SBP ≥160 mmHg, sitting DBP ≥100 mmHg at screening) * Glycated hemoglobin (HbA1c) \>12% * Mean SBP \< 90 mmHg at the run-in visit or at the screening visit * Clinical diagnosis of chronic heart failure with reduced ejection fraction (HFrEF) and persistent symptoms (New York Heart Association \[NYHA\] class II - IV) at run-in visit (class 1A recommendation for mineralcorticoid receptor antagonists \[MRAs\]) * Stroke, transient ischemic cerebral attack, acute coronary syndrome, or hospitalization for worsening heart failure, in the last 30 days prior to the screening visit * Dialysis for acute renal failure within 12 weeks of run-in visit * Renal allograft in place or scheduled within next 12 months from the run-in visit
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.2 groupes d'intervention sont désignés dans cette étude
50% de chances d'être dans le groupe placebo en aveugle
Groupes de traitement
Groupe I
ExpérimentalGroupe II
PlaceboObjectifs de l'étude
Objectifs principaux
Objectifs secondaires