News

Patients taking Kerendia saw significant reduction in cardiovascular death and hospitalization and urgent visits for heart ...
US FDA approves Bayer’s finerenone for new indication in patients with heart failure with left ventricular ejection fraction of ≥ 40%: Berlin Wednesday, July 16, 2025, 13:00 H ...
The FDA has broadened the approved use of finerenone (Kerendia) to include treatment for heart failure, according to an ...
The era of predictive modeling enhanced with machine learning and artificial intelligence (AI) to aid clinical ...
Following priority review, the U.S. Food and Drug Administration approved Bayer's Kerendia (finerenone) for the treatment of ...
Bayer’s Kerendia (finerenone) has been approved by the US Food and Drug Administration (FDA) to treat heart failure (HF) patients with left ventricular ejection fraction (LVEF) of at least 40%.
Approval of Kerendia was based on results from the Phase III FINEARTS-HF trial, which demonstrated statistically significant ...
In a significant move, the U.S. Food and Drug Administration granted approval for Kerendia for patients with heart failure ...
The FDA expanded the indication for finerenone (Kerendia) in heart failure (HF), drug manufacturer Bayer announced.
The US Food and Drug Administration has approved the use of finerenone (Kerendia) in heart failure (HF) patients with mildly ...
Kerendia was originally approved in July 2021 to reduce cardiovascular and kidney complications in patients with chronic ...
Bayer AG BAYRY announced that the FDA has approved a label expansion of kidney disease drug Kerendia (finerenone). The ...