Cipaglucosidase Alfa: First Approval

Drugs. 2023 Jun;83(8):739-745. doi: 10.1007/s40265-023-01886-5.

Abstract

Cipaglucosidase alfa (Pombiliti) is a recombinant human acid α-glucosidase (GAA) product being developed by Amicus Therapeutics along with the enzyme stabilizer miglustat as a two-component therapy for Pompe disease. Pompe disease is a rare, inherited lysosomal disease caused by a deficiency of the enzyme GAA, which leads to accumulation of glycogen in various tissues. On 27 March 2023, cipaglucosidase alfa was approved in the EU as a long-term enzyme replacement therapy (ERT) used in combination with miglustat for the treatment of adults with late-onset Pompe disease. This article summarizes the milestones in the development of cipaglucosidase alfa leading to this first approval.

Publication types

  • Review

MeSH terms

  • 1-Deoxynojirimycin / pharmacology
  • 1-Deoxynojirimycin / therapeutic use
  • Adult
  • Enzyme Replacement Therapy
  • Glycogen / therapeutic use
  • Glycogen Storage Disease Type II* / drug therapy
  • Humans

Substances

  • miglustat
  • 1-Deoxynojirimycin
  • Glycogen