Is Finerenone (finerenone) indicated for patients with chronic kidney disease (CKD) and type 2 diabetes?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Finerenone in Chronic Kidney Disease with Type 2 Diabetes

Finerenone is strongly indicated for patients with chronic kidney disease (CKD) and type 2 diabetes who have persistent albuminuria (>30 mg/g) despite maximum tolerated renin-angiotensin-aldosterone system (RAS) inhibitor therapy, with proven benefits in reducing kidney disease progression and cardiovascular events. 1

Patient Selection Criteria

Finerenone therapy is appropriate for patients who meet the following criteria:

  • Type 2 diabetes with CKD
  • Persistent albuminuria (>30 mg/g)
  • Already on maximum tolerated RAS inhibitor therapy
  • eGFR ≥25 mL/min/1.73 m²
  • Baseline serum potassium ≤4.8 mmol/L 1

Dosing Recommendations

Dosing should be based on kidney function:

  • eGFR 25-59 mL/min/1.73 m²: 10 mg once daily
  • eGFR ≥60 mL/min/1.73 m²: 20 mg once daily 1

Contraindications and Precautions

Finerenone should not be initiated in patients with:

  • Adrenal insufficiency
  • eGFR <25 mL/min/1.73 m²
  • Serum potassium >4.8 mmol/L 1

Monitoring Requirements

  • Check serum potassium at baseline
  • Recheck at 1 month after initiation
  • Continue monitoring every 4 months thereafter
  • Target serum potassium level ≤4.8 mmol/L
  • Hold finerenone if serum potassium >5.5 mmol/L 1

Clinical Benefits

Finerenone has demonstrated significant benefits in patients with CKD and type 2 diabetes:

  • Kidney disease progression: 23% reduction (HR 0.77,95% CI: 0.67-0.88)
  • Cardiovascular events: 14% reduction (HR 0.86,95% CI: 0.78-0.95)
  • Hospitalization for heart failure: 29% reduction (HR 0.71,95% CI: 0.56-0.90) 1

The FIGARO-DKD trial specifically showed that finerenone reduced the risk of hospitalization for heart failure by 29% compared to placebo (HR 0.71,95% CI: 0.56-0.90) 2. Additionally, finerenone reduced the risk of new-onset heart failure by 32% (HR 0.68,95% CI: 0.50-0.93) 2.

Advantages of Nonsteroidal MRAs

Finerenone, as a nonsteroidal mineralocorticoid receptor antagonist (MRA), offers several advantages over steroidal MRAs:

  • More balanced tissue distribution between heart and kidney
  • More potent anti-inflammatory and anti-fibrotic effects
  • Lower risk of hyperkalemia
  • Minimal hormonal side effects 1

Combination Therapy

Finerenone can be effectively combined with other medications for additive cardiorenal protection:

  • SGLT2 inhibitors (no dose adjustment required)
  • GLP-1 receptor agonists
  • Metformin (if eGFR >30 mL/min/1.73 m²) 1

Hyperkalemia Risk Management

The risk of hyperkalemia with finerenone is lower than with steroidal MRAs but still requires monitoring:

  • Incidence of hyperkalemia: 10.8% with finerenone vs. 5.3% with placebo in FIGARO-DKD
  • Discontinuation due to hyperkalemia: 2.3% with finerenone vs. 0.9% with placebo in FIDELIO-DKD 1
  • In clinical trials, treatment-emergent adverse events were balanced between finerenone and placebo groups 2

Clinical Pearls and Pitfalls

  • Always ensure patients are on maximum tolerated RAS inhibitor therapy before initiating finerenone
  • Monitor potassium levels carefully, especially in patients with risk factors for hyperkalemia
  • Do not initiate in patients with severely reduced kidney function (eGFR <25 mL/min/1.73 m²)
  • Benefits are consistent across different eGFR and albuminuria categories 3
  • Blood pressure reduction accounts for only a small proportion (12-14%) of finerenone's cardiorenal benefits 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.