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Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications
OBJECTIVES: Rare diseases are a global public health issue with a more pressing situation in China. Unfortunately, the relevant research and development in this country are still in its infancy, leading to limited drug accessibility. In view of this, the Chinese government has taken a series of coun...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375655/ https://www.ncbi.nlm.nih.gov/pubmed/37501126 http://dx.doi.org/10.1186/s13023-023-02684-8 |
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author | Zhao, Zhiyao Pei, Zhongyang Hu, Anxia Zhang, Yuhui Chen, Jing |
author_facet | Zhao, Zhiyao Pei, Zhongyang Hu, Anxia Zhang, Yuhui Chen, Jing |
author_sort | Zhao, Zhiyao |
collection | PubMed |
description | OBJECTIVES: Rare diseases are a global public health issue with a more pressing situation in China. Unfortunately, the relevant research and development in this country are still in its infancy, leading to limited drug accessibility. In view of this, the Chinese government has taken a series of countermeasures to promote orphan drug R&D in recent years, which has presented encouraging results. This paper aims to review incentive policies and funding initiatives formulated by the Chinese government and examine their implications on orphan drug R&D. METHODS: Policies targeting orphan drug R&D during 2012–2022 were retrieved from the relevant official websites, categorized into different themes and analyzed for the contents. Data on government funding, drug approval, clinical trial approval and orphan drug designation were collected through internet search to analyze the implications of those incentive policies and initiatives on orphan drug R&D in China. RESULTS: A total of 20 relevant policy documents were identified and five major themes were revealed through content analysis, including national strategy, expedited approval, safety and efficacy requirements, data protection and technical support. The government input in orphan drug R&D has witnessed a steady annual increase. Driven by those incentives, the numbers of orphan drugs approved for marketing and drug candidates entering clinical studies are increasing year by year, and more domestic pharmaceutical companies are actively involved in the R&D of orphan drugs. CONCLUSIONS: Orphan drug development in China is growing rapidly under the stimulation of incentive regulatory policies and more investment in researches. China is working toward a more standardized and comprehensive rare disease ecosystem. However, there are still some challenges, such as the lack of sufficient financial support and the call for systematic legislation on rare diseases, to be addressed for future success. |
format | Online Article Text |
id | pubmed-10375655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103756552023-07-29 Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications Zhao, Zhiyao Pei, Zhongyang Hu, Anxia Zhang, Yuhui Chen, Jing Orphanet J Rare Dis Research OBJECTIVES: Rare diseases are a global public health issue with a more pressing situation in China. Unfortunately, the relevant research and development in this country are still in its infancy, leading to limited drug accessibility. In view of this, the Chinese government has taken a series of countermeasures to promote orphan drug R&D in recent years, which has presented encouraging results. This paper aims to review incentive policies and funding initiatives formulated by the Chinese government and examine their implications on orphan drug R&D. METHODS: Policies targeting orphan drug R&D during 2012–2022 were retrieved from the relevant official websites, categorized into different themes and analyzed for the contents. Data on government funding, drug approval, clinical trial approval and orphan drug designation were collected through internet search to analyze the implications of those incentive policies and initiatives on orphan drug R&D in China. RESULTS: A total of 20 relevant policy documents were identified and five major themes were revealed through content analysis, including national strategy, expedited approval, safety and efficacy requirements, data protection and technical support. The government input in orphan drug R&D has witnessed a steady annual increase. Driven by those incentives, the numbers of orphan drugs approved for marketing and drug candidates entering clinical studies are increasing year by year, and more domestic pharmaceutical companies are actively involved in the R&D of orphan drugs. CONCLUSIONS: Orphan drug development in China is growing rapidly under the stimulation of incentive regulatory policies and more investment in researches. China is working toward a more standardized and comprehensive rare disease ecosystem. However, there are still some challenges, such as the lack of sufficient financial support and the call for systematic legislation on rare diseases, to be addressed for future success. BioMed Central 2023-07-27 /pmc/articles/PMC10375655/ /pubmed/37501126 http://dx.doi.org/10.1186/s13023-023-02684-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhao, Zhiyao Pei, Zhongyang Hu, Anxia Zhang, Yuhui Chen, Jing Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title | Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title_full | Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title_fullStr | Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title_full_unstemmed | Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title_short | Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications |
title_sort | analysis of incentive policies and initiatives on orphan drug development in china: challenges, reforms and implications |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375655/ https://www.ncbi.nlm.nih.gov/pubmed/37501126 http://dx.doi.org/10.1186/s13023-023-02684-8 |
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