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美国非制药企业推动癌症通用药物重新利用的途径

Pathways for non-manufacturers to drive generic drug repurposing for cancer in the U.S.

作者信息

Crittenden Devon, Gallagher Raquel, Milans Del Bosch Fernanda, Fox David M, Kleiman Laura B

机构信息

Reboot Rx Inc, Boston, MA, United States.

出版信息

Front Pharmacol. 2024 Oct 9;15:1419772. doi: 10.3389/fphar.2024.1419772. eCollection 2024.

Abstract

Repurposing generic drugs as new treatments for life-threatening diseases such as cancer is an exciting yet largely overlooked opportunity due to a lack of market-driven incentives. Nonprofit organizations and other non-manufacturers have been ramping up efforts to repurpose widely available generic drugs and rapidly expand affordable treatment options for patients. However, these non-manufacturers find it difficult to obtain regulatory approval in the U.S. Without a straightforward path for approval and updating drug labeling, non-manufacturers have relied on off-label use of repurposed drugs. This limits the broad clinical adoption of these drugs and patient access. In this paper, we explore the regulatory landscape for repurposing of small molecule generic drugs within the U.S. We describe case studies of repurposed drugs that have been successfully incorporated into clinical treatment guidelines for cancer without regulatory approval. To encourage greater adoption of generic drugs in clinical practice-that is, to encourage the repurposing of these drugs-we examine existing Food and Drug Administration (FDA) pathways for approval of new uses or indications for generic drugs. We show how non-manufacturers, who are generally more active in generic drug repurposing than manufacturers, could utilize existing regulatory authorities and pathways, and we describe the challenges they face. We propose an extension of the existing 505(b)(2) new drug application (NDA) approval pathway, called a "labeling-only" 505(b)(2) NDA, that would enable non-manufacturers to seek approval of new indications for well-established small molecule drugs when multiple generic products are already available. It would not require new chemistry, manufacturing, and controls (CMC) data or introducing new drug products into the marketplace. This pathway would unlock innovation broadly and enable patients to benefit from the enormous potential of low-cost generic drugs.

摘要

将仿制药重新用作治疗癌症等危及生命疾病的新疗法,是一个令人兴奋但因缺乏市场驱动激励而在很大程度上被忽视的机会。非营利组织和其他非制造商一直在加大力度,重新利用广泛可得的仿制药,并迅速为患者扩大可负担的治疗选择。然而,这些非制造商发现很难在美国获得监管批准。由于缺乏直接的批准途径和更新药品标签的途径,非制造商一直依赖重新利用药物的非标签使用。这限制了这些药物在临床上的广泛应用以及患者的可及性。在本文中,我们探讨了美国小分子仿制药重新利用的监管情况。我们描述了一些重新利用药物的案例研究,这些药物在未经监管批准的情况下已成功纳入癌症临床治疗指南。为了鼓励在临床实践中更多地使用仿制药,即鼓励这些药物的重新利用,我们研究了美国食品药品监督管理局(FDA)现有的批准仿制药新用途或新适应症的途径。我们展示了通常在仿制药重新利用方面比制造商更积极的非制造商如何利用现有的监管机构和途径,以及我们描述了他们面临的挑战。我们提议扩展现有的505(b)(2)新药申请(NDA)批准途径,称为“仅标签”505(b)(2) NDA,这将使非制造商能够在已有多种仿制药产品的情况下,寻求对成熟小分子药物新适应症的批准。它不需要新的化学、制造和控制(CMC)数据,也不需要将新药品引入市场。这条途径将广泛释放创新潜力,并使患者能够从低成本仿制药的巨大潜力中受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f0a/11496753/77657ac7a3e8/fphar-15-1419772-g001.jpg

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