Inhibitors of pcsk9

EP4766701A1Pending Publication Date: 2026-07-01DRAUPNIR BIO APS

Patent Information

Authority / Receiving Office
EP · EP
Patent Type
Applications
Current Assignee / Owner
DRAUPNIR BIO APS
Filing Date
2024-08-23
Publication Date
2026-07-01

AI Technical Summary

Technical Problem

Current therapies for lowering LDL cholesterol levels, such as statins, have limitations including side effects and increased expression of PCSK9, which counteracts their beneficial effects. Additionally, there is a need for small molecule compounds that can effectively bind PCSK9, offering improved efficacy and ease of administration compared to biologic therapies.

Method used

Development of novel small molecule PCSK9 inhibitors that modulate the activity of PCSK9 and bind to it with high affinity, providing a pharmacologically acceptable salt form for use as medicaments. These compounds are designed to overcome the drawbacks of biologic therapies by offering oral bioavailability, reduced immunogenicity, and lower costs.

Benefits of technology

The small molecule PCSK9 inhibitors effectively reduce LDL cholesterol levels and mitigate the risk of atherosclerotic cardiovascular disease events without major adverse effects, providing a more convenient and cost-effective treatment option compared to existing biologic therapies.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present disclosure relates to small molecule inhibitors of proprotein convertase subtilisin-like / kexin type 9 (PCSK9) pharmaceutical compositions comprising said compounds and their use in prevention and treatment of diseases and conditions associated with PCSK9.
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