能否拯救濒危的生物仿制药市场?需要为长期利益弥合相互竞争的利益关系

IF 5.4 2区 医学 Q1 IMMUNOLOGY
Teresa Barcina Lacosta, Arnold G. Vulto, Florian Turk, Isabelle Huys, Steven Simoens
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引用次数: 0

摘要

市场信号包括(1)开发管道中的生物仿制药数量有限,(2)生物仿制药开发仅集中于高利润治疗领域,(3)生物仿制药停产和撤出数量增加,这些都表明欧洲生物仿制药市场面临可持续性威胁。破坏可持续发展的两个突出因素是:各利益相关方之间的利益竞争,以及偏重短期收益而忽视未来的可持续发展威胁,因此需要制定有效的政策来创造生物制剂市场的可持续竞争。迄今为止,为促进生物仿制药的采用而实施的措施并不一定得到遵守,而且成效参差不齐。此外,这些政策并没有持续改善人们获得负担得起的生物制剂的机会。在本评论中,我们旨在提高人们对生物仿制药市场脆弱性的认识,以及对就具有长远眼光的政策解决方案达成一致的困难的认识。我们建议以集体行动理论为基础,推进利益相关者利益的协调。这种首创的方法可以为生物仿制药市场的长期解决方案提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Endangered Biosimilar Markets be Rescued? The Need to Bridge Competing Interests for Long-Term Gain

Market signals such as: (1) the limited number of biosimilars in the development pipeline, (2) the focus of biosimilar development on high-profit therapeutic areas only, and (3) the increase in the number of biosimilar discontinuations and withdrawals, are indicative of sustainability threats facing biosimilar markets in Europe. Two prominent factors that undermine sustainability are: competing interests between the various stakeholders and a preferential focus on short-term gains, disregarding future sustainability threats, hence the need for effective policies that create sustainable competition in biologic markets. Thus far, measures implemented to foster biosimilar adoption have not been necessarily complied with and have had mixed success. Further, these policies have not consistently led to improving access to affordable biologics. In this commentary, we aim to raise awareness of vulnerabilities of biosimilar markets and of difficulties relating to reaching an agreement on policy solutions with a long-term vision. We propose to build on knowledge from collective action theory to advance in reconciling stakeholder interests. This first-of-its-kind approach can inform long-term solutions for biosimilar markets.

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来源期刊
BioDrugs
BioDrugs 医学-免疫学
CiteScore
12.60
自引率
2.90%
发文量
50
审稿时长
>12 weeks
期刊介绍: An essential resource for R&D professionals and clinicians with an interest in biologic therapies. BioDrugs covers the development and therapeutic application of biotechnology-based pharmaceuticals and diagnostic products for the treatment of human disease. BioDrugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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