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Finerenone (Kerendia, BAY94-8862) - Phase 3 | BAYRY Pipeline | CatalystAlert

Finerenone (Kerendia, BAY94-8862)

Phase 3

00%

Phase 3

Development Phase

1

Upcoming Catalysts

0

Historical Events

1

Regulatory Approvals

Upcoming Catalysts

What are catalysts?

Q2 '27

BAYRYPhase 3$42.5B

Finerenone (Kerendia, BAY94-8862) Phase 3 Est. Readout

Finerenone (Kerendia, BAY94-8862)• Chronic Kidney Disease219

Q2 2027~QEstimated

00%

Competitive Landscape

4 competitors in Chronic Kidney Disease

JNJepoetin alfa

SNYSevelamer hydrochloride

View Full Landscape

Drug Information

Target Indication

Chronic Kidney Disease

Clinical Trial

Last updated: 12/17/2025

Patent & Exclusivity

No patent data available. Pre-approval drugs may not have Orange Book listings.

Source: FDA Orange Book

Regulatory Approvals

EMA2/16/2022

Kerendia

Kerendia is indicated for the treatment of chronic kidney disease (with albuminuria) associated with type 2 diabetes in adults. For study results with respect to renal and cardiovascular events, see section 5.1. Kerendia is indicated for the treatment of symptomatic chronic heart failure with left ventricular ejection fraction (LVEF) ≥ 40% in adults.

Drug Science

Mechanism of action & safety profile

Developer

BAYRY

BAYER

Healthcare•Europe•NASDAQ

Related Pipeline

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Colorectal Neoplasms

Amikacin Inhalation Solution (BAY41-6551)Phase 3

Pneumonia, Bacterial

Oxybutynin (Oxytrol, BAY839380)Phase 3

Overactive Bladder

D,L-lysine acetylsalicylate (Aspirin, BAY81-8781) 500 mg IVPhase 3

Acute Coronary Syndrome

EE20/DRSP (YAZ, BAY86-5300)Phase 3

Oral Contraceptive

View full pipeline

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