KERENDIA (finerenone) by Bayer is mineralocorticoid receptor antagonists [moa]. Approved for nonsteroidal mineralocorticoid-receptor antagonist [epc]. First approved in 2021.
Drug data last refreshed 10h ago · AI intelligence enriched 1w ago
KERENDIA (finerenone) is a nonsteroidal mineralocorticoid receptor antagonist (MRA) administered orally as a tablet for chronic kidney disease in patients with type 2 diabetes. It works by blocking mineralocorticoid receptors to reduce renal and cardiovascular fibrosis and inflammation. The drug represents a new mechanistic approach to kidney protection beyond standard renin-angiotensin-aldosterone system inhibitors.
Product is in peak commercial phase with $270M in Part D spending and strong uptake, indicating active brand team growth and commercial expansion.
Mineralocorticoid Receptor Antagonists
Nonsteroidal Mineralocorticoid-Receptor Antagonist
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Role of Finerenone in African American Veterans With Diabetic Kidney Disease
A Study to Learn More About How Safe Finerenone is, When it is Taken for a Longer Time With Standard Treatment, in Children and Young Adults With Heart Failure and Left Ventricular Systolic Dysfunction
An Observational Study, Called FINEXPLORER, to Learn More About How Well Finerenone Works in Adults in Spain With Chronic Kidney Disease (CKD) Linked to Type 2 Diabetes, by Looking at Changes in a CKD Risk Score
A Study to Learn More About How Safe Finerenone is and How Well it Works in Adults With Chronic Heart Failure in South Korea
Finerenone and Cardiac Remodeling
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Working on KERENDIA offers career exposure to a differentiated, first-in-class MRA with unique safety and monitoring requirements that demand medical expertise and field engagement. The peak-stage product provides solid platform for commercial acumen in a specialized therapeutic area (diabetes/nephrology), though limited clinical trial activity may constrain R&D advancement opportunities.
2 open roles linked to this drug