Drug intelligence / Profile preview

zerlasiran

Development stage
Phase 2
Lead developer
Silence Therapeutics
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

Zerlasiran is a short interfering RNA (siRNA) gene-silencing therapy in development for the treatment of patients with elevated lipoprotein(a) [Lp(a)], a genetically determined cardiovascular risk factor. It works by targeting and silencing the LPA gene, which encodes the protein component of Lp(a). By inhibiting this gene, zerlasiran significantly reduces circulating Lp(a) levels—by more than 80% on average in clinical trials—with effects persisting for up to 60 weeks after dosing. Elevated Lp(a) is associated with increased risk of atherosclerotic cardiovascular disease (ASCVD), heart attacks, and strokes. Zerlasiran is being developed by Silence Therapeutics and has completed Phase 2 trials demonstrating efficacy and safety; further Phase 3 studies are planned[1][4][5][6][7].

02

Targets

LPA (Lysophosphatidic acid)

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