πŸ›οΈ Verified NIH Record β€’ Updated 2026-06-25

A Study Called FINE-REAL to Learn More About the Use of the Drug Finerenone in a Routine Medical Care Setting (NCT05348733)

FINE-REAL: A Non-interventional Study Providing Insights Into the Use of Finerenone in a Routine Clinical Setting

πŸ”΅ Active, Not Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: Bayer

🩺 Plain-English Summary (8th-Grade Level)

This is an observational study in people with chronic kidney disease (CKD) and type 2 diabetes (T2D) who will be receiving finerenone. Kidneys filter extra water and waste out of the blood and make urine. CKD is a long-term, progressive, decrease in the kidneys' ability to filter the blood properly. In people with T2D, the body does not make enough of a hormone called insulin, or does not use insulin well enough, resulting in high blood sugar levels that can cause damage to the kidneys. As a result, CKD can occur as a complication of T2D. Finerenone works by blocking certain proteins, called mineralocorticoid receptors. An increased stimulation of these proteins is thought to damage the kidneys and the heart. By lowering their stimulation, finerenone reduces the risk of kidney disease progressively getting worse. Finerenone is available and approved for doctors to prescribe to people with CKD and T2D. Since it has only recently become available for these patients, there is a need for more information about the use of finerenone in the real-world setting. The main purpose of the study is to learn more about treatment patterns in people with CKD and T2D who just started or will start finerenone treatment as decided and prescribed by their doctor as part of their routine medical care. To answer this question, the researchers will collect data on: * Clinical characteristics (e.g., history of CKD and T2D, blood pressure, heart health) of the participants * Reasons for starting finerenone * Reasons for stopping finerenone early * How long participants have been taking finerenone (planned by their doctor compared to actual time it was taken) * Dosing of finerenone * Other medications used while taking finerenone The researchers will also collect data on medical problems (called adverse events) that the participants may have during the study. All adverse events are collected, even if they might not be related to the study treatment. Hyperkalemia, a medical term used to describe a potassium level in the blood that is higher than normal, is of special interest when finerenone is combined with some medications commonly taken to control blood pressure. Researchers want to know how often higher potassium levels occur, and when it leads to: * Stopping finerenone treatment too early * Dialysis (a medical procedure to filter the blood of extra water and waste) * Care in a hospital All data will come from medical records or from interviews study doctors will have with the participants during visits that take place during routine medical care. Participants in the US will be invited to provide voluntary blood and urine samples that could be analyzed later to better understand possible changes in protein or nucleic acid levels over time. Each participant will be in the study for 12 months. This time participating in the study may be shorter if their finerenone treatment is stopped early or the study comes to an end as planned in September 2027.

Who can join: Review the eligibility criteria below.

Location: Nephrology Consultants LLC β€” Huntsville, Alabama

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (56 Sites)

Showing the first 25 of 56 sites.

  • Nephrology Consultants LLC β€” Huntsville, Alabama
  • AKDHC Medical Research Servies LLC β€” Phoenix, Arizona
  • Harrisburg Family Medical Center β€” Harrisburg, Arkansas
  • Kidney Disease Medical Group β€” Glendale, California
  • Renal Consultants Medical Group β€” Granada Hills, California
  • University of Central Florida College of Medicine β€” Orlando, Florida
  • Gulf View Medical β€” Port Charlotte, Florida
  • Hanson Clinical Research Center β€” Port Charlotte, Florida
  • Metabolic Research Institute β€” West Palm Beach, Florida
  • Augusta University β€” Augusta, Georgia
  • Coastal Medical Research β€” Brunswick, Georgia
  • Caritas Medical Center β€” Stockbridge, Georgia
  • Herman Clinical Research LLC β€” Suwanee, Georgia
  • Laurie Tom, MD β€” Honolulu, Hawaii
  • Pacific Diabetes & Endocrine Center β€” Honolulu, Hawaii
  • Medico β€” Chicago, Illinois
  • Nephrology Associates Northern Illinois and Indiana β€” Hinsdale, Illinois
  • Kidney and Hypertension Center of Wabash Valley LLC β€” Terre Haute, Indiana
  • Ochsner Medical Foundation β€” Slidell, Louisiana
  • University of Maryland Midtown Professionals Group Healthcare β€” Baltimore, Maryland
  • NECCR Primacare Research, LLC β€” Fall River, Massachusetts
  • Healthy Heart Cardiology β€” Grand Rapids, Michigan
  • Care Access Research - Minneapolis β€” Minneapolis, Minnesota
  • Nephrology and Hypertension Associates β€” Tupelo, Mississippi
  • Renown Regional Medical Center β€” Reno, Nevada

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—