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NCT Number: NCT05348733

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

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.

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This study is active but is not currently recruiting participants.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult participants of all genders (≥18 years old)
  • Diagnosis of CKD associated with T2D based on assessment by physician.
  • Treatment according to local marketing authorization, finerenone 20 or 10 mg.Treatment should have been started up to 8 weeks before or after the ICF is signed.
  • Decision to initiate treatment with finerenone must be made before ICF is signed.
  • Signed informed consent

Exclusion criteria

  • Participation in an investigational trial at any time during the course of this study
  • Contra-indications according to the local label.

Treatment and study plan

Kerendia (Finerenone, BAY94-8862)

Drug

Decision will taken by the treating physician to initiate treatment with finerenone.

Primary outcomes

  1. Descriptive analysis of clinical characteristics of participants with chronic kidney disease (CKD) and with type 2 diabetes(T2D).

    Time frame: Approximately 62 months

  2. Descriptive summary of reasons for introducing finerenone.

    Time frame: Approximately 62 months

  3. Descriptive summary of reasons for discontinuation of finerenone.

    Time frame: Approximately 62 months

  4. Planned and actual duration of treatment with finerenone

    Time frame: Approximately 62 months

  5. Planned and actual daily dose of finerenone treatment

    Time frame: Approximately 62 months

  6. Planned and actual frequency of finerenone treatment

    Time frame: Approximately 62 months

  7. Descriptive summary of secondary therapies used in participants with CKD and T2D.

    Time frame: Approximately 62 months

Secondary outcomes

  1. Occurrence of adverse events (AEs) and serious adverse events (SAEs)

    Time frame: Approximately 62 months

  2. Occurrence of hyperkalemia

    Time frame: Approximately 62 months

    leading to permanent study drug discontinuation, dialysis or hospitalization

Other outcomes

  1. Descriptive summary for healthcare resource utilization.

    Time frame: Approximately 62 months

  2. Occurrence of newly diagnosed diabetic retinopathy or progression of existing disease at treatment initiation

    Time frame: Approximately 62 months

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Apr 27, 2022
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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