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A Study to Investigate the Effect of Lepodisiran on the Reduction of Major Adverse Cardiovascular Events in Adults With Elevated Lipoprotein(a) - ACCLAIM-Lp(a)

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NCT06292013 · readout ≤ 955 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
17,300estimated
Sites
931
Countries
Argentina, Australia, Austria +25

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-03-05actualWhen the study began enrolling
Primary completionMar 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMar 2029estimatedThe whole study's end, after follow-up
First posted2024-03-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Atherosclerotic Cardiovascular Disease (ASCVD)
  • Elevated Lp(a)

Interventions

  • Drug: Lepodisiran Sodium — also filed as LY3819469
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Time to First Occurrence of Any Component of the Major Adverse Cardiac Event (MACE)-4 Composite Endpoint
measured Baseline up to End of Study (About 4.5 Years)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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