When should Kerendia (finerenone) be initiated in patients with chronic kidney disease (CKD) and type 2 diabetes?

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Last updated: October 15, 2025View editorial policy

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Indications to Start Kerendia (Finerenone)

Kerendia (finerenone) should be initiated in patients with type 2 diabetes and chronic kidney disease who have persistent albuminuria (UACR ≥30 mg/g) despite maximum tolerated dose of RAS inhibitors, with an eGFR ≥25 mL/min/1.73 m² and normal serum potassium levels. 1

Patient Selection Criteria

  • Finerenone is indicated for patients with type 2 diabetes and CKD with albuminuria (UACR ≥30 mg/g) who are already on maximum tolerated dose of ACE inhibitor or ARB therapy 1
  • Eligible patients should have an eGFR between 25-90 mL/min/1.73 m² 1
  • Serum potassium must be ≤4.8 mmol/L before initiation 1
  • Particularly beneficial for patients at high risk of CKD progression and cardiovascular events despite standard therapy 1, 2

Dosing Algorithm

  • For patients with eGFR 25-60 mL/min/1.73 m²: Start with 10 mg once daily 1, 2
  • For patients with eGFR >60 mL/min/1.73 m²: Start with 20 mg once daily 1, 2
  • Dose increase from 10 mg to 20 mg can be considered after 1 month if serum potassium remains ≤4.8 mmol/L and eGFR is stable 1

Clinical Benefits

  • Reduces risk of CKD progression with a 23% reduction in composite kidney outcomes (sustained ≥57% decrease in eGFR or renal death) 1, 2
  • Decreases cardiovascular events with a 14% reduction in composite cardiovascular outcomes (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and hospitalization for heart failure) 1
  • Provides a 36% reduction in end-stage kidney disease compared to placebo (HR 0.64 [95% CI 0.41–0.995]) 1, 2
  • Reduces heart failure hospitalizations by 29% (HR 0.71 [95% CI 0.56–0.90]) 1, 3
  • Reduces new-onset heart failure by 32% in patients without prior heart failure history 3

Monitoring Requirements

  • Check serum potassium before initiation and periodically during treatment 1
  • Monitor serum creatinine and eGFR to assess kidney function 1
  • Watch for hyperkalemia, which occurred in 10.8% of patients on finerenone versus 5.3% on placebo in clinical trials 1
  • Treatment discontinuation due to hyperkalemia is relatively low (1.2% in the FIGARO-DKD trial) 1, 2

Combination Therapy Considerations

  • Finerenone can be used alongside SGLT2 inhibitors for complementary cardiorenal protection 2, 4
  • Recent evidence shows that combination therapy with finerenone and empagliflozin provides a 29-32% greater reduction in albuminuria compared to either agent alone 4
  • Consider finerenone after SGLT2 inhibitors in the treatment algorithm, as SGLT2 inhibitors have shown larger effects on reducing both kidney and cardiovascular outcomes 1
  • Only 4.5% of patients in the FIDELIO-DKD trial were on SGLT2 inhibitors, so most evidence for finerenone is as monotherapy or with RAS inhibitors 1

Contraindications and Cautions

  • Avoid in patients with serum potassium >4.8 mmol/L 1
  • Use with caution in patients already on ACE inhibitors or ARBs due to increased hyperkalemia risk 2
  • Patients with heart failure with reduced ejection fraction were excluded from the FIGARO-DKD trial 1, 2
  • Consider nephrology referral when eGFR <30 mL/min/1.73 m² for management of advanced kidney disease 1, 2

Common Pitfalls to Avoid

  • Failure to monitor serum potassium regularly, which is essential to prevent and manage hyperkalemia 1
  • Not checking baseline potassium levels before initiation 1
  • Starting with too high a dose in patients with reduced kidney function 1
  • Not considering finerenone in patients who remain at high risk despite SGLT2 inhibitor therapy 1, 4
  • Overlooking the potential benefits in patients with mild albuminuria (30-300 mg/g), as benefits extend across the spectrum of albuminuria 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Role of Finerenone in Heart Failure and CKD

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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