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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2023
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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. |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-10184071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT blairhannaha cipaglucosidasealfafirstapproval |