PCSK9 inhibitors: a patent review 2018-2023

Expert Opin Ther Pat. 2024 Apr;34(4):245-261. doi: 10.1080/13543776.2024.2340569. Epub 2024 Apr 11.

Abstract

Introduction: Proprotein convertase subtilisin/kexin 9 (PCSK9) plays a crucial role in breaking down the hepatic low-density lipoprotein receptor (LDLR), thereby influencing the levels of circulating low-density lipoprotein cholesterol (LDL-C). Consequently, inhibiting PCSK9 through suitable ligands has been established as a validated therapeutic strategy for combating hypercholesterolemia and cardiovascular diseases.

Area covered: Patent literature claiming novel compounds inhibiting PCSK9 disclosed from 2018 to June 2023 available in the espacenet database, which contains more than 150 million patent documents from over 100 patent-granting authorities worldwide.

Expert opinion: The undisputable beneficial influence of PCSK9 as a pharmacological target has prompted numerous private and public institutions to patent chemical frameworks as inhibitors of PCSK9. While several compounds have advanced to clinical trials for treating hypercholesterolemia, they have not completed these trials yet. These compounds must contend in a complex market where new, costly, and advanced drugs, such as monoclonal antibodies and siRNA, are prescribed instead of inexpensive and less potent statins.

Keywords: CVD; LDL-C; PCSK9; hypercholesterolemia; patents.

Publication types

  • Review

MeSH terms

  • Animals
  • Anticholesteremic Agents* / pharmacology
  • Cardiovascular Diseases* / drug therapy
  • Cholesterol, LDL* / blood
  • Drug Development
  • Humans
  • Hypercholesterolemia* / drug therapy
  • PCSK9 Inhibitors*
  • Patents as Topic*
  • Proprotein Convertase 9* / metabolism
  • Receptors, LDL / metabolism

Substances

  • PCSK9 Inhibitors
  • PCSK9 protein, human
  • Proprotein Convertase 9
  • Cholesterol, LDL
  • Anticholesteremic Agents
  • Receptors, LDL