Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

A Study to Determine the Efficacy and Safety of Finerenone on Morbidity and Mortality Among Hospitalized Heart Failure Patients

NCT06008197 · View on ClinicalTrials.gov ↗

Study Summary

Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients hospitalized with acute decompensated heart failure (HF) and mildly reduced or preserved left ventricular ejection fraction.

Interventions

  • DRUG Placebo
  • DRUG Finerenone

Study Locations (20)

Indiana

  • Indianapolis, IN Investigative Site 10074 — Indianapolis
  • Indianapolis, IN Investigative Site 10008 — Indianapolis
  • Merrillville, IN Investigative Site 10064 — Merrillville

Kentucky

  • Louisville, KY Investigative Site 10006 — Louisville
  • Louisville, KY Investigative Site 10086 — Louisville
  • Paducah, KY Investigative Site 10079 — Paducah

California

  • Huntington Beach, CA Investigative Site 10031 — Huntington Beach
  • Los Angeles, CA Investigative Site 10089 — Los Angeles

Florida

  • Brooksville, FL Investigative Site 10077 — Brooksville
  • Miramar, FL Investigative Site 10113 — Miramar

Ohio

  • Centerville, OH Investigative Site 10119 — Centerville
  • Cincinnati, OH Investigative Site 10088 — Cincinnati

Arizona

  • Glendale, AZ Investigative Site 10096 — Glendale

Idaho

  • Boise, Idaho Investigative Site 10073 — Boise

Illinois

  • Chicago, IL Investigative Site 10062 — Chicago

Trial Details

FieldValue
Enrollment Target 5,200 participants
Start Date 2024-01-17
Est. Completion 2027-12
Phase Phase 3

Sponsor

Colorado Prevention Center

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06008197

The ClinicalTrials.gov registry entry for NCT06008197 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 5,200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Colorado Prevention Center, which has 33 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Heart Failure appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06008197 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Indiana, Kentucky, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06008197 about?

NCT06008197 is a clinical study titled "A Study to Determine the Efficacy and Safety of Finerenone on Morbidity and Mortality Among Hospitalized Heart Failure Patients". Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients hospitalized with acute decompensated heart failure (HF) and mildly reduced or preserved left ventricular ejection fraction.

What is the current status of trial NCT06008197?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 5,200 participants. The study started on 2024-01-17. Estimated completion is 2027-12.

What conditions does trial NCT06008197 study?

This clinical trial studies the following conditions: Heart Failure, Acute Heart Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06008197?

The interventions under investigation include: Placebo (DRUG), Finerenone (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06008197?

This trial is sponsored by Colorado Prevention Center, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06008197 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Idaho, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial