Drug intelligence / Profile preview

YS2302018 + laroprovstat

Development stage
Preclinical
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

YS2302018 + AZD0780 is an investigational oral combination therapy being developed by AstraZeneca for the treatment of dyslipidemia, hypercholesterolemia, and other cardiovascular diseases. The combination consists of two oral small-molecule agents: YS2302018, a preclinical lipoprotein(a) [Lp(a)] disruptor originally discovered by CSPC Pharmaceutical Group and licensed by AstraZeneca in 2024, and AZD0780 (laroprovstat), AstraZeneca's clinical-stage oral proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. YS2302018 binds to apolipoprotein(a) [Apo(a)] to prevent its assembly with apolipoprotein B-100 [ApoB-100], thereby blocking the formation of atherogenic Lp(a) particles. AZD0780 binds to the C-terminal domain of PCSK9, preventing PCSK9-mediated degradation of low-density lipoprotein receptors (LDLR) and enhancing the clearance of LDL cholesterol. By combining these two complementary mechanisms, the therapy aims to simultaneously lower both LDL-C and Lp(a) levels, addressing key residual cardiovascular risk factors in patients with dyslipidemia.

Other names
AZD0780 + YS2302018AZD0780 and YS2302018AZD-0780 and YS2302018AZD 0780 and YS2302018YS2302018 + AZD0780YS2302018 + laroprovstatYS2302018 and AZD0780YS-2302018 and AZD0780YS 2302018 and AZD0780YS2302018 and laroprovstatYS-2302018 and laroprovstatYS 2302018 and laroprovstatlaroprovstat + YS2302018laroprovstat and YS2302018
02

Targets

PCSK9 (Proprotein convertase subtilisin/kexin type 9)

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