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在低收入和中等收入国家实现单克隆抗体公平可及的新方法。

Novel approaches to enable equitable access to monoclonal antibodies in low- and middle-income countries.

作者信息

Malhotra Shelly, Cameron Anne-Isabelle, Gotham Dzintars, Burrone Esteban, Gardner Peter J, Loynachan Colleen, Morin Sébastien, Scott Cherise P, Pérez-Casas Carmen

机构信息

Global Access, IAVI, New York, New York, United States of America.

Strategy, Unitaid, Geneva, Switzerland.

出版信息

PLOS Glob Public Health. 2024 Jul 1;4(7):e0003418. doi: 10.1371/journal.pgph.0003418. eCollection 2024.

Abstract

Monoclonal antibodies (mAbs) are revolutionizing management of non-communicable diseases in high-income countries and are increasingly being advanced for a range of infectious diseases (IDs). However, access to existing mAbs is limited in low- and middle-income countries (LMICs), and investment in developing fit-for-purpose mAbs for IDs that disproportionately affect LMICs has been limited. Underlying these access barriers are systemic challenges, including a lack of commercial incentives to target LMIC markets and complexity in manufacturing and regulatory processes. Novel strategies are needed to overcome systemic access barriers for mAbs. We outline key areas where new approaches could address these barriers, based on a multistakeholder consultation in March 2023. Three disease-market archetypes are identified to guide thinking about business models tailored to different contexts. New business models are needed to incentivize development and manufacturing of ID mAbs and to ensure mAbs are optimized with a target product profile and cost of goods that enable use in diverse LMIC settings. Lessons can be applied from voluntary licensing strategies and product development partnerships that have shown success in catalysing development and affordable supply for a range of infectious diseases. Technology transfer will be key to expand LMIC research and manufacturing capacity and to enable sustainable and diversified supply. Improved market intelligence, demand aggregation mechanisms, and portfolio-based manufacturing models could be used to de-risk commercial investment and establish a sustainable manufacturing ecosystem for affordable mAbs. Novel regulatory approaches and robust technology transfer may reduce data requirements and timelines for biosimilar approvals. Trailblazer products, with coordinated "end-to-end" support from funders, can demonstrate proof of concept for pathways to accessible mAbs across a broader range of LMICs. Research funders; local, regional, global health agencies; and, private sector partners should commit to implementing innovative partnerships and end-to-end strategies that enable equitable access to mAbs for infectious diseases in LMICs.

摘要

单克隆抗体(mAbs)正在彻底改变高收入国家非传染性疾病的管理方式,并且越来越多地被用于一系列传染病(IDs)的治疗。然而,在低收入和中等收入国家(LMICs),获取现有单克隆抗体的机会有限,而且针对对LMICs影响尤为严重的传染病研发适用单克隆抗体的投资也很有限。这些获取障碍的背后存在系统性挑战,包括缺乏针对LMIC市场的商业激励措施以及制造和监管流程的复杂性。需要新的策略来克服单克隆抗体的系统性获取障碍。基于2023年3月的多方利益相关者协商,我们概述了新方法可以解决这些障碍的关键领域。确定了三种疾病 - 市场原型,以指导针对不同情况量身定制商业模式的思考。需要新的商业模式来激励传染病单克隆抗体的研发和生产,并确保单克隆抗体根据目标产品概况和商品成本进行优化,以便在不同的LMIC环境中使用。可以从自愿许可策略和产品开发伙伴关系中吸取经验教训,这些策略在促进一系列传染病的研发和可负担供应方面已取得成功。技术转让将是扩大LMIC研究和制造能力以及实现可持续和多样化供应的关键。改进的市场情报、需求聚合机制和基于组合的制造模式可用于降低商业投资风险,并建立一个可持续的负担得起的单克隆抗体制造生态系统。新颖的监管方法和强大的技术转让可能会减少生物类似药批准的数据要求和时间线。在资助者的协调“端到端”支持下的开拓者产品,可以证明在更广泛的LMICs中获取单克隆抗体途径的概念验证。研究资助者、地方、区域、全球卫生机构以及私营部门合作伙伴应致力于实施创新伙伴关系和端到端战略,以确保LMICs公平获取用于传染病的单克隆抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be1e/11216602/31b5f6ab69ea/pgph.0003418.g001.jpg

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