Gene editing shot aims to permanently lower bad cholesterol
NCT ID NCT07839936
First seen Sep 24, 2026 · Last updated Sep 25, 2026 · Updated 1 time
Summary
Researchers are testing a one-time gene editing medicine called VERVE-102 in adults who have plaque buildup in their arteries or are at high risk for it. The trial compares VERVE-102 to a placebo to see how much it lowers LDL cholesterol. About 175 people will receive either the medicine or the placebo through an IV. The goal is to find out if a single treatment can reduce the need for ongoing cholesterol-lowering drugs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- VERVE-102, a one-time gene editing medicine given by IV
- What this could lead to
- If it works, a single IV treatment could lower bad cholesterol for years, possibly replacing daily pills or regular injections for people with inherited high cholesterol.
- What could go wrong
- This is a phase 2 trial, so researchers do not yet know if the gene editing is safe or effective. The body might not respond as hoped, or the effect could fade over time. Gene editing carries unknown long-term risks.
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 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 175 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2030
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.
- Ages
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18 to 70 years
- 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: * Established atherosclerotic cardiovascular disease (ASCVD) and/or at a high risk of ASCVD Exclusion Criteria: * History of confirmed or suspected homozygous familial hypercholesterolemia (HoFH) * Chronic liver disease * Current treatment with PCSK9 inhibitor or prior treatment within specified timeframe
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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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Epic Medical Research
DeSoto, Texas, 75115, United States
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