Microbicide Research Branch (MRB), Prevention Sciences Program (PSP), Division of AIDS (DAIDS), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Department of Health and Human Services (HHS), 6700-B Rockledge Drive, Room 5118, Bethesda, MD 20892 USA.
Drug Deliv Transl Res. 2011 Jun;1(3):194-200. doi: 10.1007/s13346-011-0034-2. Epub 2011 May 21.
The efforts of the topical microbicide field to identify a safe and effective topical microbicide were realized in July of 2010 with the reporting of the results of the Centre for the AIDS Programme of Research in South Africa 004 trial. In this trial, a 1% tenofovir gel was found to reduce women's risk for HIV acquisition by 39% compared to placebo. To understand the impact of this trial on future microbicide development, we must view it from the historical perspective of previous phases 2 and 3 clinical trials with detergents and sulfated polyanions. This knowledge and emerging information must then be parlayed into the next steps needed to create a safe, effective, and acceptable topical microbicide. This review will look at the lessons learned from preclinical and clinical development of topical microbicides, focusing on two significant future challenges: (1) topical microbicide formulation safety and (2) the critical role that adherence to product use has in determining safety and efficacy in clinical trials and ultimately commercial viability of the licensed product. In addition to framing these issues within our current understanding of formulation and prevention of HIV acquisition, recent advances in our understanding of the mechanism of HIV transmission and how it informs on future formulation strategies will be briefly discussed.
局部杀微生物剂领域为鉴定安全有效的局部杀微生物剂所付出的努力在 2010 年 7 月取得了成果,当时报道了南非艾滋病规划署研究中心 004 试验的结果。在该试验中,与安慰剂相比,1%的替诺福韦凝胶使女性感染艾滋病毒的风险降低了 39%。为了了解该试验对未来杀微生物剂开发的影响,我们必须从以前使用清洁剂和硫酸多阴离子的 2 期和 3 期临床试验的历史角度来看待它。然后,必须将这些知识和新出现的信息转化为创造安全、有效和可接受的局部杀微生物剂所需的下一步骤。这篇综述将回顾局部杀微生物剂的临床前和临床开发中吸取的经验教训,重点关注两个重大的未来挑战:(1)局部杀微生物剂配方的安全性;(2)在临床试验中,坚持使用产品对于确定安全性和疗效以及最终获得许可产品的商业可行性的关键作用。除了在我们目前对配方和预防艾滋病毒感染的理解框架内提出这些问题外,还将简要讨论我们对艾滋病毒传播机制的理解的最新进展,以及它如何为未来的配方策略提供信息。