Cipaglucosidase Alfa: First Approval

25Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

Blair, H. A. (2023). Cipaglucosidase Alfa: First Approval. Drugs, 83(8), 739–745. https://doi.org/10.1007/s40265-023-01886-5

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free