Study Purpose: To determine the safety and efficacy of Finerenone along with standard of care, on the progression of kidney disease in patients with Non-Diabetic Chronic Kidney Disease. To be enrolled in this study, you must meet certain requirements. You may be eligible to participate if you meet the following criteria: Study Duration: approximately 33 to 50 months Study Commitment: screening - 1-14 days intervention - 32 to approximately 49 months follow-up - approximately 1 month Age: 18 years old Sex: Male and Female Conditions/Eligibility: Clinical diagnosis of chronic kidney disease and: eGFR >= 25 but <=90 mL/min and UACR of >=500 but <=3500 mg/g at screening. on stable and max dose of an ACEi or ARB for at least 4 weeks prior to screening. K+ <=4.8 mmol/L at screening. Study Procedures: Vital signs, Physical Exam, ECG, Questionnaires, Medical History, bloodwork, urine collection, Study Drug administration. Compensation: $100 / visit