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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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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2009
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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. |
format | Text |
id | pubmed-2777019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT saengerpaul currentstatusofbiosimilargrowthhormone |