A Study to See if Lepodisiran Can Reduce Plaque in Coronary Arteries of Adults With Elevated Lp(a) Who Have Had Heart Events or Are at High Risk
Eli Lilly and Company · NCT07613294
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 45–80 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 252
- US sites recruiting
- 13
- Study start
- June 1, 2026
- Record last updated
- October 8, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Lipoprotein(a), also known as Lp(a), is a protein that carries cholesterol and proteins in your blood. People with high Lp(a) have a higher risk for heart disease. The main purpose of the study is to investigate how lepodisiran, compared to a placebo, affects the amount and type of plaque in the heart's vessels using an imaging technology known as Coronary Computed Tomography Angiography (CCTA) in adults who have high levels of Lp(a).
Participation will last about 120 weeks.
Being studied: Lepodisiran; Placebo
Conditions: Atherosclerosis; Cardiovascular Diseases; Lipoprotein(a)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Have an Lp(a) ≥175 nmol/L
- Have established cardiovascular (CV) disease or are at risk for a first CV event
- Have angiographic evidence of coronary artery disease on screening CCTA
- If taking lipid-lowering medications, inclusive of statins or prescription strength niacin and PCSK9 inhibitors, these should be stable for 8 weeks
Exclusion Criteria
- Have had a major CV event less than 60 days before measurement of the Lp(a) level used for eligibility or uncontrolled high blood pressure at screening
- Have moderate to severe renal dysfunction
- Have severe heart failure
- Have a history of coronary artery bypass graft surgery (CABG)
- Have a planned coronary angiography, percutaneous coronary intervention (PCI), coronary artery bypass graft, or valvular intervention
- Have had a procedure to remove lipoproteins from the blood or received therapy specifically targeting Lp(a)
- Are unable to safely undergo CCTA due to medication intolerance, contrast allergies, or anatomical/technical factors
Recruiting US locations
Valley Clinical Trials, Inc.
Northridge, CA 91325
Site contact: 818-678-4900
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Torrance, CA 90502
Site contact: 424-201-3000
Jellinger and Lerman, MD PA dba The Center for Diabetes and Endocrine Care
Fort Lauderdale, FL 33312
Site contact: 954-963-7100
Jacksonville Center for Clinical Research
Jacksonville, FL 32216
Site contact: 904-730-0101
Merritt Island Medical Research, LLC
Merritt Island, FL 32952
Site contact: David Kirk
Inpatient Research Clinic
Miami Lakes, FL 33014
Site contact: 786-502-4303
Clinical Site Partners, LLC dba Flourish Research
Winter Park, FL 32789
Site contact: 407-740-8078
Profound Research LLC
Farmington Hills, MI 48334
Site contact: 947-254-1920
Vector Clinical Trials
Las Vegas, NV 89128
Site contact: 702-750-000
Heart and Vascular Research at WellSpan Health
York, PA 17403
Site contact: 717-851-2441
Intermountain Medical Center
Murray, UT 84107
Site contact: 801-507-4707
Carilion Clinic
Roanoke, VA 24014
Site contact: Lana Wahid
Eastside Research Associates
Redmond, WA 98052
Site contact: 425-869-6828
Study contacts (from the official record)
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or · 317-615-4559 · LillyTrials@Lilly.com
- Physicians interested in becoming principal investigators please contact · clinical_inquiry_hub@lilly.com
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