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Study details
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A Study to Learn More About How Well the Study Treatment Finerenone Works

Bayer
NCT IDNCT05196035ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

219

Study length

about 5.4 years

Ages

0.5–17

Locations

19 sites in AZ, CA, DC +12

What this study is about

This trial is testing whether finerenone, taken with an ACE inhibitor or angiotensin receptor blocker, helps reduce protein in urine for children with chronic kidney disease. Researchers will also examine how well finerenone works and its safety profile.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Finerenone (Kerendia, BAY94-8862)
  • 2.Take Placebo

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

finerenone

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Percent change in Urinary protein-to-creatinine ratio (UPCR) reduction from baseline to day 180+/-7

Secondary: Change in eGFR from baseline to day 180±7, Change in serum creatinine from baseline to day 180±7, Change in systolic blood pressure from baseline to day 180±7, Number participants with treatment emergent adverse events (TEAEs), Pharmacokinetics (PK) finerenone AUCτ,md, Pharmacokinetics (PK) finerenone Cmax, md

Body systems

Renal