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Current Status of Biosimilar Growth Hormone

As the first wave of biopharmaceuticals is set to expire, biosimilars or follow-on protein products (FOPPs) have emerged. The regulatory foundation for these products is more advanced and better codified in Europe than in the US. Recent approval of biosimilar Somatropin (growth hormone) in Europe an...

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Detalles Bibliográficos
Autor principal: Saenger, Paul
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777019/
https://www.ncbi.nlm.nih.gov/pubmed/19956705
http://dx.doi.org/10.1155/2009/370329
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author Saenger, Paul
author_facet Saenger, Paul
author_sort Saenger, Paul
collection PubMed
description As the first wave of biopharmaceuticals is set to expire, biosimilars or follow-on protein products (FOPPs) have emerged. The regulatory foundation for these products is more advanced and better codified in Europe than in the US. Recent approval of biosimilar Somatropin (growth hormone) in Europe and the US prompted this paper. The scientific viability of biosimilar growth hormone is reviewed. Efficacy and safety data (growth rates, IGF-1 generation) for up to 7 years for pediatric indications measure up favorably to previously approved growth hormones as reference comparators. While the approval in the US is currently only for treatment of growth hormone deficiency (GHD) in children and adults, the commercial use of approved biosimilar growth hormones will allow in the future for in-depth estimation of their efficacy and safety in non-GH deficient states as well.
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spelling pubmed-27770192009-12-02 Current Status of Biosimilar Growth Hormone Saenger, Paul Int J Pediatr Endocrinol Review Article As the first wave of biopharmaceuticals is set to expire, biosimilars or follow-on protein products (FOPPs) have emerged. The regulatory foundation for these products is more advanced and better codified in Europe than in the US. Recent approval of biosimilar Somatropin (growth hormone) in Europe and the US prompted this paper. The scientific viability of biosimilar growth hormone is reviewed. Efficacy and safety data (growth rates, IGF-1 generation) for up to 7 years for pediatric indications measure up favorably to previously approved growth hormones as reference comparators. While the approval in the US is currently only for treatment of growth hormone deficiency (GHD) in children and adults, the commercial use of approved biosimilar growth hormones will allow in the future for in-depth estimation of their efficacy and safety in non-GH deficient states as well. Hindawi Publishing Corporation 2009 2009-09-29 /pmc/articles/PMC2777019/ /pubmed/19956705 http://dx.doi.org/10.1155/2009/370329 Text en Copyright © 2009 Paul Saenger. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Saenger, Paul
Current Status of Biosimilar Growth Hormone
title Current Status of Biosimilar Growth Hormone
title_full Current Status of Biosimilar Growth Hormone
title_fullStr Current Status of Biosimilar Growth Hormone
title_full_unstemmed Current Status of Biosimilar Growth Hormone
title_short Current Status of Biosimilar Growth Hormone
title_sort current status of biosimilar growth hormone
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777019/
https://www.ncbi.nlm.nih.gov/pubmed/19956705
http://dx.doi.org/10.1155/2009/370329
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