Drug data last refreshed 17h ago · AI intelligence enriched 1mo 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.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Learn More About How Well Finerenone Works in Real-world in People With Type 2 Diabetes and Chronic Kidney Disease in Primary Care (IMSS= Instituto Mexicano Del Seguro Social)
Role of Finerenone in African American Veterans With Diabetic Kidney Disease
An Observational Study to Learn More About How Safe Finerenone is and How Well it Works in Indian People With Chronic Kidney Disease and Type 2 Diabetes in Routine Medical Practice
An Observational Study Called FIRST-2.0 China to Learn More About the Use of the Study Treatment Finerenone Including How Safe it is and How Well it Works Under Real-world Conditions in a Chinese Population.
An Observational Study to Learn More About How Safe Finerenone is and How Well it Works in People With Chronic Kidney Disease and Type 2 Diabetes in Routine Medical Care in the United States
Worked on KERENDIA at Bayer? Share your interview experience or compensation data (+7 days Pro)
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.
Upgrade to Pro to access patent cliff timelines and LOE dates and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access Medicare Part D spending data and other premium pharma intelligence.
Upgrade to Pro — $25/mo$270M Medicare spend — this is a commercially significant brand
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