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Cell line access to revolutionize the biosimilars market

Biologic drugs are notoriously expensive. Biosimilars, though priced lower, are also costly. Analysis of the cost of production of biologics suggests that the cost of manufacture is in many cases less than 10% of the price in high-income countries, and less than a third of the price of biosimilars i...

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Autor principal: Gotham, Dzintars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051195/
https://www.ncbi.nlm.nih.gov/pubmed/30057752
http://dx.doi.org/10.12688/f1000research.14808.1
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author Gotham, Dzintars
author_facet Gotham, Dzintars
author_sort Gotham, Dzintars
collection PubMed
description Biologic drugs are notoriously expensive. Biosimilars, though priced lower, are also costly. Analysis of the cost of production of biologics suggests that the cost of manufacture is in many cases less than 10% of the price in high-income countries, and less than a third of the price of biosimilars in India. This in turn implies that the relatively high prices of biosimilars are largely due to the need to undertake laborious reverse-engineering and phase 3 trials to demonstrate clinical similarity. In this article, it is proposed that originators could be required to submit cell line stocks to regulators and disclose details of manufacturing processes. These would be shared with prospective non-originator manufacturers to greatly reduce the investments needed to bring a non-originator biologic to market. This system would allow far greater price reductions for biologics after the expiry of monopoly rights (e.g. patents), while maintaining the monopoly rights used to incentivize drug development.
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spelling pubmed-60511952018-07-27 Cell line access to revolutionize the biosimilars market Gotham, Dzintars F1000Res Opinion Article Biologic drugs are notoriously expensive. Biosimilars, though priced lower, are also costly. Analysis of the cost of production of biologics suggests that the cost of manufacture is in many cases less than 10% of the price in high-income countries, and less than a third of the price of biosimilars in India. This in turn implies that the relatively high prices of biosimilars are largely due to the need to undertake laborious reverse-engineering and phase 3 trials to demonstrate clinical similarity. In this article, it is proposed that originators could be required to submit cell line stocks to regulators and disclose details of manufacturing processes. These would be shared with prospective non-originator manufacturers to greatly reduce the investments needed to bring a non-originator biologic to market. This system would allow far greater price reductions for biologics after the expiry of monopoly rights (e.g. patents), while maintaining the monopoly rights used to incentivize drug development. F1000 Research Limited 2018-05-03 /pmc/articles/PMC6051195/ /pubmed/30057752 http://dx.doi.org/10.12688/f1000research.14808.1 Text en Copyright: © 2018 Gotham D http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Opinion Article
Gotham, Dzintars
Cell line access to revolutionize the biosimilars market
title Cell line access to revolutionize the biosimilars market
title_full Cell line access to revolutionize the biosimilars market
title_fullStr Cell line access to revolutionize the biosimilars market
title_full_unstemmed Cell line access to revolutionize the biosimilars market
title_short Cell line access to revolutionize the biosimilars market
title_sort cell line access to revolutionize the biosimilars market
topic Opinion Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051195/
https://www.ncbi.nlm.nih.gov/pubmed/30057752
http://dx.doi.org/10.12688/f1000research.14808.1
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