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中国孤儿药开发的激励政策和举措分析:挑战、改革与启示

Analysis of Incentive Policies and Initiatives on Orphan Drug Development in China: Challenges, Reforms and Implications.

机构信息

School of Foreign Languages, China Pharmaceutical University, Nanjing, China.

Institute of Epidemiology and Health Care, University College London, London, UK.

出版信息

Orphanet J Rare Dis. 2023 Jul 27;18(1):220. doi: 10.1186/s13023-023-02684-8.

Abstract

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.

摘要

目的

罕见病是一个全球性的公共卫生问题,在中国的情况更为紧迫。不幸的是,该国在这方面的相关研究和开发仍处于起步阶段,导致药物可及性有限。有鉴于此,中国政府近年来采取了一系列措施来促进孤儿药的研发,这取得了令人鼓舞的成果。本文旨在回顾中国政府制定的孤儿药研发激励政策和资金举措,并考察其对孤儿药研发的影响。

方法

从相关官方网站上检索了 2012-2022 年期间针对孤儿药研发的政策,将其分为不同主题进行分析,并对内容进行分析。通过互联网搜索收集了政府资金、药物批准、临床试验批准和孤儿药指定的数据,以分析这些激励政策和举措对中国孤儿药研发的影响。

结果

共确定了 20 份相关政策文件,通过内容分析揭示了五个主要主题,包括国家战略、加速审批、安全性和疗效要求、数据保护和技术支持。政府对孤儿药研发的投入逐年稳步增长。在这些激励措施的推动下,获准上市的孤儿药和进入临床试验的候选药物数量逐年增加,越来越多的国内制药公司积极参与孤儿药的研发。

结论

在中国,激励性监管政策和对研究的更多投资刺激下,孤儿药的开发正在迅速发展。中国正在朝着一个更加规范和全面的罕见病生态系统迈进。然而,未来要取得成功,仍存在一些挑战,如缺乏足够的财政支持和对罕见病的系统立法的呼吁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2adf/10375655/8c1e06ea46b3/13023_2023_2684_Fig1_HTML.jpg

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