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Lepodisiran

Alternative Names: Lepodisiran, LY3819469, LY 3819469, LY-3819469
Latest Update: 2025-04-18
Latest Update Note: Clinical Trial Update

Product Description

a short interfering RNA directed at hepatic production of apolipoprotein(a), and the effect on lipoprotein(a) serum concentrations (Sourced from: https://jamanetwork.com/journals/jama/fullarticle/2811935#google_vignette)

Mechanisms of Action: siRNA

Novel Mechanism: Yes

Modality: N/A

Route of Administration: N/A

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Eli Lilly
Company Location: INDIANAPOLIS IN 46285
Company CEO: David A. Ricks
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lepodisiran

Countries in Clinic: Argentina, Australia, Austria, Belgium, Brazil, Canada, China, Czech Republic, Denmark, France, Germany, Greece, Hungary, India, Israel, Italy, Japan, Korea, Mexico, Netherlands, Poland, Puerto Rico, Romania, Singapore, Slovakia, Spain, Taiwan, United Kingdom, United States

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Atherosclerosis|Coronary Disease|Myocardial Infarction|Stroke

Phase 2: Other

Phase 1: Healthy Volunteers|Kidney Diseases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

jRCT2051230205

P3

Not yet recruiting

Unknown

2029-05-31

J3L-MC-EZEF

P3

Recruiting

Atherosclerosis

2029-03-01

J3L-MC-EZEF

P3

Unknown Status

Coronary Disease|Stroke|Myocardial Infarction

2028-12-09

J3L-MC-EZEH

P1

Not yet recruiting

Healthy Volunteers

2026-01-01

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