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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Finerenone (Kerendia, BAY94-8862)
  • 2.Take Placebo
PhasePhase 3
DrugBAY94-8862
Routeoral
Primary goalPercent change in Urinary protein-to-creatinine ratio (UPCR) reduction from baseline to day 180+/-7

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low11%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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