FDA approves Kerendia for heart failure with ejection fraction of 40% or higher

Published Date: 16 Jul 2025

Following priority review, the U.S. Food and Drug Administration approved Bayer's Kerendia (finerenone) for the treatment of patients with heart failure with left ventricular ejection fraction (LVEF) ≥40%.

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A new study underscores the importance of monitoring patients’ cardiometabolic health soon after starting ADT plus ARPI therapy for prostate cancer.

Women make up less than 10% of oversight committee seats for interventional structural heart disease trials, although women are being studied more intently than ever before.

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Non-vitamin K oral anticoagulant use was associated with modestly slower cognitive decline and lower risks for death and stroke in adults with comorbid Alzheimer’s disease and atrial fibrillation.

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