Finerenone (Kerendia, BAY94-8862) + Placebo

Phase 3Recruiting
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Interest: 44/100
44
Hype Score

Development Stage

Pre-clinical
Phase 1
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Left Ventricular Systolic Dysfunction

Conditions

Left Ventricular Systolic Dysfunction, Heart Failure (Pediatric)

Trial Timeline

Nov 19, 2025 → Dec 30, 2029

About Finerenone (Kerendia, BAY94-8862) + Placebo

Finerenone (Kerendia, BAY94-8862) + Placebo is a phase 3 stage product being developed by Bayer for Left Ventricular Systolic Dysfunction. The current trial status is recruiting. This product is registered under clinical trial identifier NCT07188805. Target conditions include Left Ventricular Systolic Dysfunction, Heart Failure (Pediatric).

What happened to similar drugs?

0 of 3 similar drugs in Left Ventricular Systolic Dysfunction were approved

Approved (0) Terminated (0) Active (3)

Hype Score Breakdown

Clinical
17
Activity
15
Company
12
Novelty
0
Community
0

Clinical Trials (3)

NCT IDPhaseStatus
NCT07188805Phase 3Recruiting
NCT05196035Phase 3Recruiting
NCT05013008Phase 2Completed