Finerenone
Aldosterone Antagonists
Sold as KERENDIA
- Drug class
- Aldosterone Antagonists
- Availability
- See label
- Routes
- Oral
- Markets covered
- 3
- Products on record
- 7
Overview
Finerenone is an active pharmaceutical ingredient in the Aldosterone Antagonists group (C03DA). The information below is compiled per regulator from the product labels on record, with direct links to the original documents.
Regulatory status by market
| Market | Regulator | Products | Last revision |
|---|---|---|---|
| GB United Kingdom | MHRA | 3 | June 2, 2026 |
| CA Canada | Health Canada | 3 | February 10, 2026 |
| EU European Union | EMA | 1 | May 7, 2026 |
GBUnited Kingdom· MHRA
3 products
Uses
Kerendia is indicated for the treatment of chronic kidney disease (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults. Kerendia is indicated for the treatment of symptomatic chronic heart failure with left ventricular ejection fraction (LVEF) ≥ 40% in adults.
How to take
CACanada· Health Canada
3 products
Side effects & warnings
).
Legend:
C=Case Study; CT=Clinical Trial; T=Theoretical Note: The effects of itraconazole, clarithromycin, fluvoxamine, rifampicin and efavirenz on finerenone exposure are predictions based on PBPK simulations. No clinical data was available to evaluate effects of strong and weak CYP3A4 inhibitors or strong and moderate CYP3A4 inducers on finerenone exposure.
75 h), compared to administration under fasted conditions. This was paralleled by an increase in extent of absorption (AUC). 75 h), and increase in AUC. 3 Pharmacokinetics, Effect of food). 25 hours and Cmax decreased by approximately 23%.
4 Administration). Concomitant intake of grapefruit or grapefruit juice is expected to increase the plasma concentration of finerenone and should be avoided (see 4 Dosage and Administration and 7 Warnings and Precautions, General). 6 Drug-Herb Interactions Avoid concomitant use of KERENDIA with St John’s Wort (a strong CYP3A4 inducer) which may markedly decrease finerenone exposure and result in reduced therapeutic effect.
EUEuropean Union· EMA
1 product
Uses
Kerendia is indicated for the treatment of chronic kidney disease (with albuminuria) associated with type 2 diabetes in adults. 1. Kerendia is indicated for the treatment of symptomatic chronic heart failure with left ventricular ejection fraction (LVEF) ≥ 40% in adults.
How to take
Sources & citations
- [1]MHRA (UK) · PLGB000100752 · revised May 1, 2026
- [2]Health Canada (DPD) · 02531917 · revised February 10, 2026
- [3]European Medicines Agency · EMEA/H/C/005200 · revised May 7, 2026
Information on this page is compiled from public regulatory records. Drugvu is not affiliated with any regulator or pharmaceutical manufacturer. This is not medical advice. Always consult a qualified healthcare professional.