Finerenone
| Clinical data | |
|---|---|
| Trade names | Kerendia | 
| Other names | BAY 94-8862 | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a621038 | 
| License data | 
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| Pregnancy category | 
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| Routes of administration | Oral | 
| Drug class | Potassium-sparing diuretic | 
| ATC code | |
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| CAS Number | |
| PubChem CID | |
| DrugBank | |
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| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.247.614 | 
| Chemical and physical data | |
| Formula | C21H22N4O3 | 
| Molar mass | 378.432 g·mol−1 | 
| 3D model (JSmol) | |
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Finerenone, marketed under the brand name Kerendia among others, is a medication used to reduce the risk of kidney function decline, kidney failure, cardiovascular death, non-fatal heart attacks, and hospitalization for heart failure in adults with chronic kidney disease associated with type 2 diabetes. Finerenone is a non-steroidal mineralocorticoid receptor antagonist. It is taken orally (swallowed by mouth).
Common side effects include abnormally high levels of potassium in the bloodstream, abnormally low levels of sodium in the bloodstream, and abnormally low blood pressure.
Finerenone was approved for medical use in the United States in July 2021, and in the European Union in February 2022. The US Food and Drug Administration considers it to be a first-in-class medication.