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VisitWhich drug will be the main competitor to KERENDIA® in the HFmrEF and HFpEF market by end of 2024?
Entresto (Novartis) • 25%
Farxiga (AstraZeneca) • 25%
Jardiance (Boehringer Ingelheim) • 25%
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Industry reports and market analysis from firms like IMS Health or IQVIA
Bayer's Finerenone Achieves Primary Endpoint in Phase III HFmrEF and HFpEF Study
Aug 5, 2024, 06:40 AM
Bayer has announced that its Phase III FINEARTS-HF cardiovascular outcomes study investigating KERENDIA® (finerenone) in patients with heart failure with mildly reduced or preserved ejection fraction has achieved its primary endpoint. The study showed that finerenone, a non-steroidal MRA, demonstrated definitive cardiovascular benefits in patients with heart failure with mildly reduced ejection fraction (HFmrEF) and heart failure with preserved ejection fraction (HFpEF), including reductions in CVd+total HF events. The results are seen as key to unlocking blockbuster sales for the drug. Full results will be presented at the upcoming ESC Congress.
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