Ten years of biosimilar recombinant human growth hormone in Europe

Paul Saenger Division of Pediatric Endocrinology, Department of Pediatrics, Winthrop University Hospital, Mineola, NY, USA Abstract: Recombinant human growth hormone (rhGH) has been in clinical use for more than 30 years. With the expiration of patent exclusivity for the first wave of rhGH product...

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Main Author: Saenger P
Format: Article
Language:English
Published: Dove Medical Press 2017-05-01
Series:Drug Design, Development and Therapy
Subjects:
Online Access:https://www.dovepress.com/ten-years-of-biosimilar-recombinant-human-growth-hormone-in-europe-peer-reviewed-article-DDDT
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spelling doaj-726081644b334ef39a551a08d487e72d2020-11-25T00:12:06ZengDove Medical PressDrug Design, Development and Therapy1177-88812017-05-01Volume 111505150732865Ten years of biosimilar recombinant human growth hormone in EuropeSaenger PPaul Saenger Division of Pediatric Endocrinology, Department of Pediatrics, Winthrop University Hospital, Mineola, NY, USA Abstract: Recombinant human growth hormone (rhGH) has been in clinical use for more than 30 years. With the expiration of patent exclusivity for the first wave of rhGH products and other biopharmaceuticals, the opportunity emerged for the development of biosimilar medicines. A biosimilar is defined by the European Medicines Agency (EMA) as a biological medicine that is similar to another biological medicine that has already been authorized for use. The EMA led the way (well ahead of the Food and Drug Administration in the US) in developing the biosimilar concept, and the type of science-based regulatory framework required to ensure high-quality, safe, and effective biosimilar medicines; the provisions for approval of biosimilars have been in place in Europe since 2005. Under these provisions, Omnitrope® was approved by the EMA in 2006 as the world’s first biosimilar medicine; 2016 therefore marks the 10th anniversary of its approval in Europe. A substantial data set, based on clinical development studies and 10 years of postapproval use, has now accumulated for biosimilar rhGH; this data set shows that the product is an effective treatment option for children who require rhGH treatment, and has a safety profile that is consistent with the rhGH class. The decade since the EMA approved biosimilar rhGH has seen the successful approval and clinical use of 20 biosimilar medicines, confirming the integrity of the scientific basis for the biosimilar concept, as well as the quality of regulatory decision-making. Keywords: recombinant human growth hormone, Omnitrope®, biosimilarhttps://www.dovepress.com/ten-years-of-biosimilar-recombinant-human-growth-hormone-in-europe-peer-reviewed-article-DDDTbiosimilarsOmnitrope®
collection DOAJ
language English
format Article
sources DOAJ
author Saenger P
spellingShingle Saenger P
Ten years of biosimilar recombinant human growth hormone in Europe
Drug Design, Development and Therapy
biosimilars
Omnitrope®
author_facet Saenger P
author_sort Saenger P
title Ten years of biosimilar recombinant human growth hormone in Europe
title_short Ten years of biosimilar recombinant human growth hormone in Europe
title_full Ten years of biosimilar recombinant human growth hormone in Europe
title_fullStr Ten years of biosimilar recombinant human growth hormone in Europe
title_full_unstemmed Ten years of biosimilar recombinant human growth hormone in Europe
title_sort ten years of biosimilar recombinant human growth hormone in europe
publisher Dove Medical Press
series Drug Design, Development and Therapy
issn 1177-8881
publishDate 2017-05-01
description Paul Saenger Division of Pediatric Endocrinology, Department of Pediatrics, Winthrop University Hospital, Mineola, NY, USA Abstract: Recombinant human growth hormone (rhGH) has been in clinical use for more than 30 years. With the expiration of patent exclusivity for the first wave of rhGH products and other biopharmaceuticals, the opportunity emerged for the development of biosimilar medicines. A biosimilar is defined by the European Medicines Agency (EMA) as a biological medicine that is similar to another biological medicine that has already been authorized for use. The EMA led the way (well ahead of the Food and Drug Administration in the US) in developing the biosimilar concept, and the type of science-based regulatory framework required to ensure high-quality, safe, and effective biosimilar medicines; the provisions for approval of biosimilars have been in place in Europe since 2005. Under these provisions, Omnitrope® was approved by the EMA in 2006 as the world’s first biosimilar medicine; 2016 therefore marks the 10th anniversary of its approval in Europe. A substantial data set, based on clinical development studies and 10 years of postapproval use, has now accumulated for biosimilar rhGH; this data set shows that the product is an effective treatment option for children who require rhGH treatment, and has a safety profile that is consistent with the rhGH class. The decade since the EMA approved biosimilar rhGH has seen the successful approval and clinical use of 20 biosimilar medicines, confirming the integrity of the scientific basis for the biosimilar concept, as well as the quality of regulatory decision-making. Keywords: recombinant human growth hormone, Omnitrope®, biosimilar
topic biosimilars
Omnitrope®
url https://www.dovepress.com/ten-years-of-biosimilar-recombinant-human-growth-hormone-in-europe-peer-reviewed-article-DDDT
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