Insights into Support Systems for Orphan Drug Development: A Comparative Study.

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Ye Leng, Yu Tang, Weijie Yu, Yiru Hou, Hanqing He, Yanjie Han, Huiyao Huang, Wenbao Zhang, Ning Li
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Abstract

Due to great unmet medical needs, orphan drug development is a common issue of high priority for policymakers, industry leaders, researchers and patients worldwide. The establishment of a harmonized support system is the way forward to address the dilemma facing rare diseases (RDs). This study pioneers the proposal of a framework and dimensions of support systems affecting orphan drug development, covering legal (political and legal basis), technical (regulatory guidance and acceleration), motivational (economic incentives and innovation returns) and logistical (fundamental infrastructure) factors. This study, based on the framework, shows that the conditions for orphan drug development above are basically developed in the US, the EU and China. Additionally, China lags behind in terms of economic incentives and fundamental infrastructure. Continuous improvements in pricing and reimbursement, as well as the acceleration of real-world data (RWD) database and biobank repository integration, are expected in China. Based on these findings from the three study regions, action plans with three strategies (national plans and strategies, a patient-centered health system, global governance and collaborations) and eleven actions are suggested for strengthening synergies between initiatives and stakeholders to satisfy the medical needs of RD patients and families. This study can provide a reference not only for orphan drug development in the three study regions but also for all other countries worldwide, especially for those with a late start in addressing RDs.

孤儿药开发支持系统的洞察:一项比较研究。
由于大量未满足的医疗需求,孤儿药开发是全球决策者、行业领导者、研究人员和患者高度重视的共同问题。建立一个统一的支持系统是解决罕见病面临的困境的前进方向。本研究率先提出了影响孤儿药开发的支持系统的框架和维度,包括法律(政治和法律基础)、技术(监管指导和加速)、动机(经济激励和创新回报)和后勤(基本基础设施)因素。基于该框架的研究表明,上述孤儿药开发条件在美国、欧盟和中国基本具备。此外,中国在经济激励和基础设施方面落后。在定价和报销方面的持续改进,以及实际数据(RWD)数据库和生物库存储库整合的加速,有望在中国实现。基于这三个研究区域的研究结果,提出了包含三个战略(国家计划和战略、以患者为中心的卫生系统、全球治理和合作)的行动计划和11项行动,以加强倡议和利益相关者之间的协同作用,以满足RD患者和家庭的医疗需求。本研究不仅可以为三个研究区域的孤儿药开发提供参考,也可以为世界上其他国家,特别是起步较晚的国家提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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