Can a cholesterol-lowering combo also shrink fatty liver in diabetic heart patients?
NCT ID NCT07736313
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This trial investigates whether adding a PCSK9 inhibitor to a high-intensity statin can reduce liver fat—measured by a non-invasive FibroScan—in diabetic patients who have recently had a heart attack or unstable angina. Half the participants will receive the combination therapy, while the other half receive the statin alone. The goal is to see if the combination offers additional benefits for liver health and cholesterol control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a PCSK9 inhibitor (a cholesterol-lowering drug) plus rosuvastatin 20 mg tablet
- What this could lead to
- If it works, this could point toward a way to both lower cholesterol and reduce liver fat in diabetic heart patients, potentially lowering their risk of future heart problems.
- What could go wrong
- This is a small, early-phase trial (120 people) focused on a liver fat measurement, not on actual heart events. The added benefit over statins alone may be modest, and PCSK9 inhibitors can cause injection-site reactions or muscle pain.
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.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 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: 1. Age ≥18y.o 2. Any patient presented with acute coronary syndromes (Myocardial infarction (MI), non-ST elevation Myocardial infarction (NSTEMI), unstable angina) underwent coronary angiography within admission. 3. Patients must be diabetic. 4. Statin naïve patients at the time of enrollment. Exclusion Criteria: 1. patients \> 18 y.o 2. Patients who have chronic liver disease other than MASLD 3. Patients having liver neoplasm 4. Patient refused
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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 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.
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