医学
人类免疫缺陷病毒(HIV)
梅德林
重症监护医学
病毒学
政治学
法学
作者
François Venter,Monica Gandhi,Simiso Sokhela,Kenly Sikwese,Helen Bygrave,Louis Da Gama,Ndiviwe Mphothulo,Lise Jamieson,Mark J. Siedner,Anton Pozniak,Pablo Rojo,Solange Baptiste,Jacque Wambui,Gesine Meyer‐Rath,Brian Honermann,Mitchell Warren,Linda‐Gail Bekker,Phumla Sinxadi,Simon Collins,Jessica Burry
出处
期刊:The Lancet HIV
[Elsevier BV]
日期:2024-08-16
卷期号:11 (10): e711-e716
被引量:9
标识
DOI:10.1016/s2352-3018(24)00173-5
摘要
Large randomised studies of new long-acting medications for the prevention and treatment of HIV have shown high effectiveness and acceptability. Although modelling studies indicate these agents could be fundamental in HIV elimination, coordination of their entry into health-care markets is crucial, especially in low-income and middle-income countries with high HIV prevalence, where coordination is low despite UNAIDS flagging that global HIV targets will not be met. Research and implementation projects are tightly controlled by originator pharmaceutical companies, with only a small percentage of eligible people living with or affected by HIV benefiting from these projects. WHO, financial donors, manufacturers, and governments need to consider urgent coordinated action from stakeholders worldwide, akin to the successful introduction of dolutegravir into treatment programmes across low-income and middle-income countries. Without this immediate coordination, large-scale access to long-acting agents for HIV will be delayed, potentially extending into the 2030s. This delay is unacceptable considering the established global HIV targets.
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