Center for Global Health Science and Security, Department of Microbiology and Immunology, Georgetown University, Washington, District of Columbia, United States of America.
PLoS Negl Trop Dis. 2023 Jan 12;17(1):e0011010. doi: 10.1371/journal.pntd.0011010. eCollection 2023 Jan.
The availability and accessibility of safe and effective drugs, vaccines, and diagnostics are essential to reducing the immense global burden of neglected tropical diseases (NTDs). National regulatory authorities, such as the United States Food and Drug Administration (FDA), play an essential role in this effort to ensure access to safe and effective medical products by working within a set of legal frameworks and regulatory functions. However, medical product development for NTDs remains neglected, as combating NTDs is not a viable commercial market for pharmaceutical companies. To spur research and development (R&D) of NTD products, the US government has authorized various programs and policies to engage pharmaceutical companies, many of which provide FDA with the legal authority to implement NTD programs and pathways. Thus, this review provides a clear overview of the various regulatory pathways and programs employed by the FDA to increase the availability of NTD drugs, vaccines, and diagnostics. The review assesses the available information on various regulatory considerations and their impact on NTD product development as a first step in estimating the importance of such programs. Next, findings related to currently approved NTD products through these programs are discussed. Lastly, gaps in NTD R&D are identified and suggestions on how to address these are presented. The available data shows that while such incentive programs are factored into companies' decisions to pursue NTD R&D, approved products for NTDs remains vastly insufficient. Most approved products that utilize these NTD regulatory pathways and programs are overwhelmingly for tuberculosis and malaria-both of which are not considered NTDs by the World Health Organization (WHO). Dedicated efforts are needed to facilitate and accelerate NTD product including employing multiple incentive programs, regular assessment of such programs, and leveraging on public-private partnerships.
安全有效药物、疫苗和诊断试剂的供应和可及性对于减轻被忽视的热带病(NTD)的巨大全球负担至关重要。国家监管机构,如美国食品和药物管理局(FDA),在通过在一系列法律框架和监管职能内工作来确保获得安全有效的医疗产品方面发挥着重要作用。然而,针对 NTD 的药物开发仍然被忽视,因为抗击 NTD 对制药公司来说不是一个可行的商业市场。为了刺激 NTD 产品的研发(R&D),美国政府授权了各种计划和政策来吸引制药公司,其中许多计划为 FDA 提供了实施 NTD 计划和途径的法律权力。因此,本综述清楚地概述了 FDA 为增加 NTD 药物、疫苗和诊断试剂的可及性而采用的各种监管途径和计划。该综述评估了关于各种监管考虑因素及其对 NTD 产品开发的影响的可用信息,作为评估这些计划重要性的第一步。其次,讨论了通过这些计划获得批准的 NTD 产品的相关信息。最后,确定了 NTD 研发中的差距,并提出了如何解决这些差距的建议。现有数据表明,虽然这些激励计划是公司考虑开展 NTD 研发的因素之一,但针对 NTD 的获批产品仍然远远不足。通过这些 NTD 监管途径和计划获得批准的大多数产品主要是针对结核病和疟疾,而这两种疾病均不被世界卫生组织(WHO)视为 NTD。需要做出专门努力来促进和加速 NTD 产品的开发,包括采用多种激励计划、定期评估这些计划以及利用公私合作伙伴关系。