FIDELIO-DKDFinerenona y cuidado estándar para retrasar la progresión de la enfermedad renal en la diabetes tipo 2
Este estudio tiene como objetivo evaluar la efectividad de Finerenone, en combinación con el cuidado estándar, en retrasar la progresión de la enfermedad renal en individuos con Diabetes Tipo 2, observando la primera ocurrencia de insuficiencia renal, una disminución sostenida en la función renal, o muerte renal.
Finerenone (BAY94-8862)
+ Placebo
Enfermedades Urogenitales+10
+ Diabetes Mellitus Tipo 2
+ Enfermedades del Sistema Endocrino
Estudio de Tratamiento
Resumen
Fecha de inicio: 17 de septiembre de 2015
Fecha en la que se inscribió al primer participante.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.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 5734 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
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 Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.2 grupos de intervención están designados en este estudio
50% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalGrupo II
PlaceboObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios