NephrologyPhase IVEnrolling

FINE-REAL: Finerenone in Routine Clinical Practice

Chronic Kidney Disease with Type 2 Diabetes

Study Overview

A prospective, non-interventional study evaluating real-world treatment patterns, safety outcomes, and healthcare utilization in CKD patients with Type 2 Diabetes treated with finerenone, a novel non-steroidal mineralocorticoid receptor antagonist.

Inclusion Criteria

  • Adults aged 18 years or older
  • Diagnosis of CKD with Type 2 Diabetes
  • Physician decision to initiate finerenone treatment
  • Currently on optimized RAS inhibitor therapy (ACEi or ARB)

Exclusion Criteria

  • Participation in an interventional clinical trial
  • Contraindications per local finerenone labeling
  • Known hypersensitivity to finerenone or excipients
  • Baseline serum potassium >5.0 mmol/L

Study Details

Phase
Phase IV
Duration
36 months
Location
Main Facility
Compensation
No cost for study participation
Check Eligibility

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