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长效口服和注射药物防治疟疾:更新的目标产品概况。

Chemoprevention of malaria with long-acting oral and injectable drugs: an updated target product profile.

机构信息

MMV Medicines for Malaria Venture, Route de Pré-Bois 20, Post Box 1826, 1215, Geneva 15, Switzerland.

Malaria Research and Training Center, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.

出版信息

Malar J. 2024 Oct 18;23(1):315. doi: 10.1186/s12936-024-05128-1.

Abstract

Malaria is preventable, but the burden of disease remains high with over 249 million cases and 608,000 deaths reported in 2022. Historically, the most important protective interventions have been vector control and chemopreventive medicines with over 50 million children receiving seasonal malaria chemoprevention in the year 2023. Two vaccines are approved and starting to be deployed, bringing additional protection for children up to 36 months. However, the impact of these currently available tools is somewhat limited on various fronts. Vaccines exhibit partial efficacy, are relatively costly, and not accessible in all settings. The challenges encountered with chemoprevention are barriers to acceptability and feasibility, including frequency of dosing, and the lack of options in the first trimester of pregnancy and for women living with HIV. Also, the emergence of resistance against chemopreventive medicines is concerning. To address these limitations, a target product profile (TPP) is proposed as a road map to guide innovation and to boost the quest for novel chemopreventive alternatives. This TPP describes the ideal product attributes, while acknowledging potential trade-offs that may be needed. Critically, it considers the target populations most at risk; primarily infants, children, and pregnant women. Malaria control and elimination requires appropriate chemoprevention, not only in areas of high endemicity and transmission, but also in lower transmission areas where immunity is declining, as well as for travellers from areas where malaria has been eliminated. New medicines should show acceptable safety and tolerability, with high and long protective efficacy. Formulations and costs need to support operational adherence, access, and effectiveness. Next generation long-acting oral and injectable drugs are likely to constitute the backbone of malaria prevention. Therefore, the perspectives of front-line experts in malaria prevention, researchers, and those involved in drug development are captured in the TPP. This inclusive approach aims at concentrating efforts and aligning responses across the community to develop new and transformative medicines.

摘要

疟疾是可预防的,但疾病负担仍然很高,2022 年报告的病例超过 2.49 亿例,死亡 60.8 万人。从历史上看,最重要的保护干预措施一直是病媒控制和化学预防药物,2023 年有超过 5000 万儿童接受季节性疟疾化学预防。两种疫苗已获得批准并开始部署,为 36 个月以下的儿童提供额外保护。然而,这些现有工具在各个方面的影响都有些有限。疫苗的效果并不完全,成本相对较高,并且在所有环境中都无法获得。化学预防中遇到的挑战是可接受性和可行性的障碍,包括给药频率,以及在妊娠早期和 HIV 感染者中缺乏选择。此外,抗化学预防药物的耐药性也令人担忧。为了解决这些限制,提出了目标产品概况(TPP)作为指导创新和寻求新型化学预防替代品的路线图。该 TPP 描述了理想的产品属性,同时承认可能需要进行权衡。至关重要的是,它考虑了面临最大风险的目标人群;主要是婴儿、儿童和孕妇。疟疾控制和消除需要适当的化学预防,不仅在高流行和传播地区,而且在免疫下降的低传播地区,以及从疟疾已消除地区的旅行者。新药应该具有可接受的安全性和耐受性,具有高且长期的保护效果。制剂和成本需要支持操作遵守、获得和有效性。新一代长效口服和注射药物很可能构成疟疾预防的骨干。因此,疟疾预防的一线专家、研究人员和药物开发者的观点都被纳入了 TPP。这种包容性方法旨在集中精力,协调社区的反应,开发新的变革性药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26e5/11490162/d45b6ff0bd24/12936_2024_5128_Fig1_HTML.jpg

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