Zilucoplan: First Approval

Drugs. 2024 Jan;84(1):99-104. doi: 10.1007/s40265-023-01977-3.

Abstract

Zilucoplan (Zilbrysq®) is a subcutaneously administered macrocyclic peptide inhibitor of complement component 5 (C5 inhibitor) being developed by UCB for the treatment of generalised myasthenia gravis (gMG). Zilucoplan received its first approval, in Japan, in September 2023 for the treatment of gMG in adult patients who inadequately respond to steroids or other immunosuppressants and are positive for anti-acetylcholine receptor (AChR) antibodies. Subsequently, zilucoplan was approved in the USA in October 2023 for the treatment of gMG in adult patients who are anti-AChR antibody positive and in the EU in December 2023 as an add-on to standard therapy for the treatment of gMG in adult patients who are anti-AChR antibody positive. Zilucoplan is also currently under regulatory review in Australia and Canada for use in the treatment of gMG. This article summarises the milestones in the development of zilucoplan leading to this first approval for gMG.

Publication types

  • Review

MeSH terms

  • Adult
  • Autoantibodies
  • Complement C5
  • Humans
  • Myasthenia Gravis* / drug therapy
  • Peptides, Cyclic*
  • Receptors, Cholinergic

Substances

  • zilucoplan
  • Receptors, Cholinergic
  • Complement C5
  • Autoantibodies
  • Peptides, Cyclic