Eli Lilly Phase 2 Lipoprotein(a) Study Hits Primary Endpoint

Dow Jones
03-31
 

By Colin Kellaher

 

Eli Lilly said an experimental drug nearly eliminated an inherited type of bad cholesterol at its highest dose in a mid-stage study.

Eli Lilly on Sunday said the Phase 2 study of lepodisiran, designed to lower the production of lipoprotein(a), or lp(a), met its primary endpoint, reducing lp(a) levels by an average of 93.9% over the 60- to 180-day period after treatment with the highest tested dose of 400 milligrams.

The Indianapolis drugmaker said study participants who received the 16-milligram and 96-milligram lepodisiran doses saw reductions of 40.8% and 75.2% in lp(a) levels, respectively.

About 20% of Americans have high levels of lp(a), which is genetic and has been linked to increased risk for heart attack, stroke and other cardiovascular diseases. There are currently no FDA-approved drugs to lower lp(a) levels.

Eli Lilly said it will continue to evaluate the potential benefits of lepodisiran in an ongoing Phase 3 study.

 

Write to Colin Kellaher at colin.kellaher@wsj.com

 

(END) Dow Jones Newswires

March 31, 2025 06:56 ET (10:56 GMT)

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