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Study details
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A Study to Evaluate Finerenone on Clinical Efficacy and Safety in Patients with Heart Failure Who Are Intolerant or Not Eligible for Treatment with Steroidal Mineralocorticoid Receptor Antagonists

Colorado Prevention Center
NCT IDNCT06033950ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

2,600

Study length

about 3.7 years

Ages

18+

Locations

4 sites in AL, CA, MO +1

About this study

Researchers are testing whether Finerenone, a treatment, is effective and safe compared to placebo in people with heart failure who cannot take steroidal mineralocorticoid receptor antagonists (sMRA). The trial will last 1349 days.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Finerenone
  • 2.Take Placebo
PhasePhase 3
DrugFinerenone
Routeoral
Primary goalNumber of adverse events leading to discontinuation of study drug

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
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: Number of adverse events leading to discontinuation of study drug., Number of serious adverse events

Secondary: Change in Kansas City Cardiomyopathy Questionnaire Total Symptom Score (KCCQ-TSS) from baseline to Month 6.

Body systems

Cardiology / Heart