Heart failure drug finerenone under Real-World safety watch in korea
NCT ID NCT07379840
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study observes 300 adults in South Korea with chronic heart failure who are prescribed finerenone as part of their usual care. Researchers will track side effects and treatment satisfaction over one year. The goal is to see how safe and effective finerenone is in everyday medical practice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- finerenone
- What this could lead to
- If successful, this study could confirm that finerenone is safe and effective for South Korean patients with chronic heart failure.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be less reliable. It only tracks routine care, so it cannot prove cause and effect.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult chronic HF patients with LVEF ≥40% prescribed finerenone in routine clinical practice in Korea
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Adults aged 19 years or older * With informed consent from subject or legal representative (Prioritizing patient consent) * Finerenone naïve patients who are prescribed finerenone for treatment of chronic HF with LVEF ≥40% Exclusion criteria: * Contraindication according to the local label (including known hypersensitivity to the drug substance or any of its components) * Patients participating in an investigational program with interventions outside of routine clinical practice (NYHA classes II-IV) in accordance with local label
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Many Locations
RECRUITINGMultiple Locations, South Korea
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Other studies related to the condition(s) this trial covers.
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