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Eli Lilly's Lepodisiran Achieves 94.8% Reduction in Genetic Cholesterol in Phase 2 Trial

The injectable drug, targeting lipoprotein(a), moves to Phase 3 trials to assess its impact on cardiovascular events, with no serious adverse effects reported.

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Eli Lilly logo is shown on one of the company's offices in San Diego, California, U.S., September 17, 2020.
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© Sakurra via Shutterstock

Overview

  • Lepodisiran, an experimental drug by Eli Lilly, reduced lipoprotein(a) levels by 93.9% after six months and 94.8% after one year with a second dose in Phase 2 trials.
  • The drug uses RNA-targeting technology to prevent the production of lipoprotein(a), a genetic cholesterol linked to heart disease and strokes.
  • Phase 2 trials involving 320 participants reported no serious adverse events, marking a significant step in the drug's development.
  • Lepodisiran has now progressed to Phase 3 trials to determine if lowering lipoprotein(a) reduces cardiovascular events, with patient enrollment ongoing and expected to conclude this year.
  • Other pharmaceutical companies, including Amgen, Novartis, and Silence Therapeutics, are also developing treatments for lipoprotein(a), reflecting a competitive landscape in this field.