FIDELIO-DKDFinerenone and Standard Care for Delaying Kidney Disease Progression in Type 2 Diabetes
This study aims to evaluate the effectiveness of Finerenone, in combination with standard care, in delaying the progression of kidney disease in individuals with Type 2 Diabetes, by observing the first occurrence of kidney failure, a sustained decrease in kidney function, or renal death.
Finerenone (BAY94-8862)
+ Placebo
Urogenital Diseases+17
+ Chronic Disease
+ Diabetes Mellitus
Treatment Study
Summary
Study start date: September 17, 2015
Actual date on which the first participant was enrolled.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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.5734 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
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
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives