Policy strategies for inclusion of pregnant and lactating women in vaccine research.

IF 2.7 Health affairs scholar Pub Date : 2025-02-19 eCollection Date: 2025-03-01 DOI:10.1093/haschl/qxaf035
Danielle E Serota, Chelsea M Crooks, Emma E McGinty, Sallie R Permar, Laura Riley
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Abstract

Pregnant and lactating women (PLW) have historically been excluded from vaccine research, creating inequities in vaccine access and uptake for PLW. US federal research policies create the framework for inclusion of diverse populations, including PLW, in research. We conducted a policy analysis and interviews (n = 29) with experts in vaccine research for PLW to characterize the existing policy landscape and to identify policy strategies to promote inclusion of PLW in vaccine trials. We integrated policy analysis and interview results to inform 5 policy recommendations. Current federal policy does not require or incentivize the inclusion of PLW in vaccine trials. The Food and Drug Administration (FDA) guidance on inclusion of PLW in vaccine and other clinical research is nonbinding and lacks clarity. Extant policies do not adequately allay liability concerns among vaccine developers. To address these concerns, we recommend that US Congress pass legislation authorizing the FDA to require inclusion of PLW in vaccine research; incentivize sponsors to complete timely vaccine studies in PLW; create a national no-fault compensation program for clinical research participants, including PLW; remove pregnancy from the "vulnerable population" designation in FDA human subjects regulations; and clarify existing federal regulations pertaining to clinical research with PLW.

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将孕妇和哺乳期妇女纳入疫苗研究的政策战略。
孕妇和哺乳期妇女历来被排除在疫苗研究之外,这造成了孕妇和哺乳期妇女在疫苗获取和吸收方面的不平等。美国联邦研究政策创造了将包括PLW在内的不同人群纳入研究的框架。我们对PLW疫苗研究专家进行了政策分析和访谈(n = 29),以表征现有政策格局,并确定促进将PLW纳入疫苗试验的政策策略。我们将政策分析和访谈结果结合起来,为5项政策建议提供信息。目前的联邦政策并不要求或鼓励将PLW纳入疫苗试验。美国食品和药物管理局(FDA)关于将PLW纳入疫苗和其他临床研究的指南是无约束力的,缺乏明确性。现有的政策不能充分减轻疫苗开发人员对责任的担忧。为了解决这些问题,我们建议美国国会通过立法,授权FDA要求将PLW纳入疫苗研究;激励发起人及时完成PLW的疫苗研究;为包括PLW在内的临床研究参与者建立国家无过错赔偿计划;将怀孕从FDA人类受试者法规的“弱势群体”指定中删除;并澄清与PLW临床研究有关的现有联邦法规。
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