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Cipaglucosidase Alfa: First Approval

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 t...

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Detalles Bibliográficos
Autor principal: Blair, Hannah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184071/
https://www.ncbi.nlm.nih.gov/pubmed/37184753
http://dx.doi.org/10.1007/s40265-023-01886-5
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author Blair, Hannah A.
author_facet Blair, Hannah A.
author_sort Blair, Hannah A.
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description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-023-01886-5.
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spelling pubmed-101840712023-05-16 Cipaglucosidase Alfa: First Approval Blair, Hannah A. Drugs AdisInsight Report 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-023-01886-5. Springer International Publishing 2023-05-15 2023 /pmc/articles/PMC10184071/ /pubmed/37184753 http://dx.doi.org/10.1007/s40265-023-01886-5 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle AdisInsight Report
Blair, Hannah A.
Cipaglucosidase Alfa: First Approval
title Cipaglucosidase Alfa: First Approval
title_full Cipaglucosidase Alfa: First Approval
title_fullStr Cipaglucosidase Alfa: First Approval
title_full_unstemmed Cipaglucosidase Alfa: First Approval
title_short Cipaglucosidase Alfa: First Approval
title_sort cipaglucosidase alfa: first approval
topic AdisInsight Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184071/
https://www.ncbi.nlm.nih.gov/pubmed/37184753
http://dx.doi.org/10.1007/s40265-023-01886-5
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