Schaefer Robin, Donaldson L, Chigome A, Escudeiro Dos Santos M, Lamprianou S, Ndembi N, Nwokike J I, Nyambayo P, Palmi V, Renaud F, Gonzalez Tome M, Miller V
Forum for Collaborative Research, University of California, Berkeley, Washington, DC, USA.
South African Health Products Regulatory Authority, Pretoria, South Africa.
Drug Saf. 2025 Mar;48(3):209-216. doi: 10.1007/s40264-024-01494-6. Epub 2025 Jan 26.
HIV-prevention efforts focusing on women of child-bearing potential are needed to end the HIV epidemic in the African region. The use of antiretroviral drugs as pre-exposure prophylaxis (PrEP) is a critical HIV prevention tool. However, safety data on new antiretrovirals during pregnancy are often limited because pregnant people are excluded from drug development studies. Calls from communities, healthcare professionals, and regulators to improve the information supporting decision-making around the use of medical products during pregnancy have been increasing. Post-marketing safety surveillance is an essential tool for detecting adverse outcomes and evaluating real-world, longer-term effects of drugs. Detecting and evaluating uncommon pregnancy outcomes requires large sample sizes, highlighting the benefits of and need for safety surveillance. Surveillance systems vary widely across Africa, and the need for enhanced surveillance of PrEP use during pregnancy highlights the limitations of current regulatory and surveillance systems. Challenges include weak regulation and insufficient resources. Pooling of resources and regulatory harmonization could address resource challenges. The African Medicines Agency, as a specialized agency of the African Union, has the potential to improve African medical product regulation, including post-marketing safety surveillance. This can strengthen regulation and ensure that market authorization holders meet their responsibility to invest in post-marketing surveillance systems, such as pregnancy registries. At the same time, independent post-marketing studies are needed to ensure generation of essential safety data. The Forum for Collaborative Research has initiated a project to facilitate interactions between regulators in Africa, the USA, and Europe, as well as other stakeholders, and to work toward consensus on safety data generation from PrEP during pregnancy before and after marketing authorization.
为了在非洲地区终结艾滋病流行,需要针对有生育潜力的女性开展艾滋病预防工作。使用抗逆转录病毒药物作为暴露前预防(PrEP)是一种关键的艾滋病预防工具。然而,由于孕妇被排除在药物研发研究之外,新型抗逆转录病毒药物在孕期的安全性数据往往有限。社区、医疗保健专业人员和监管机构要求改善有关孕期使用医疗产品决策的信息支持,这种呼声日益高涨。上市后安全监测是检测不良后果和评估药物实际长期影响的重要工具。检测和评估罕见的妊娠结局需要大样本量,这凸显了安全监测的益处和必要性。非洲各地的监测系统差异很大,加强孕期PrEP使用监测的需求凸显了当前监管和监测系统的局限性。挑战包括监管薄弱和资源不足。资源整合和监管协调可以应对资源方面的挑战。非洲药品管理局作为非洲联盟的一个专门机构,有潜力改善非洲的医疗产品监管,包括上市后安全监测。这可以加强监管,并确保市场授权持有人履行其投资于上市后监测系统(如妊娠登记处)的责任。与此同时,需要开展独立的上市后研究,以确保生成重要的安全数据。合作研究论坛已启动一个项目,以促进非洲、美国和欧洲的监管机构以及其他利益相关者之间的互动,并努力就PrEP在孕期上市前和上市后的安全数据生成达成共识。