Cipaglucosidase Alfa: First Approval

被引:18
作者
Blair, Hannah A. [1 ]
机构
[1] Springer Nat, Private Bag 65901, Mairangi Bay, Auckland 0754, New Zealand
关键词
D O I
10.1007/s40265-023-01886-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cipaglucosidase alfa (Pombiliti((TM))) is a recombinant human acid alpha-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.
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收藏
页码:739 / 745
页数:7
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