Suppr超能文献

福沙那韦:推进HIV蛋白酶抑制剂治疗方案

Fosamprenavir: advancing HIV protease inhibitor treatment options.

作者信息

Becker Stephen, Thornton Lorna

机构信息

Pacific Horizon Medical Group, 2351 Clay Street, Suite 512, San Francisco, CA 94115, USA.

出版信息

Expert Opin Pharmacother. 2004 Sep;5(9):1995-2005. doi: 10.1517/14656566.5.9.1995.

Abstract

Fosamprenavir, the prodrug formulation of amprenavir, is a protease inhibitor recently approved in the US for the treatment of HIV infection. This agent combines the pharmacological profile of amprenavir with a low pill burden and flexible dosing schedule. Three large international trials have been completed. In treatment-naive patients, fosamprenavir, both ritonavir-boosted and -unboosted, met primary end points of non-inferiority against nelfinavir. Among naive patients, no protease inhibitor mutations emerged in those failing the boosted fosamprenavir regimen. Boosted fosamprenavir was compared to lopinavir/ritonavir in treatment-experienced patients. Non-inferiority was not achieved but similar numbers of patients achieved viral suppression when fosamprenavir was dosed twice-daily. Fosamprenavir demonstrates a favourable lipid profile in naive patients, and a low incidence of adverse effects. Fosamprenavir, as with lopinavir/ritonavir, distinguishes itself among other protease inhibitors with its potent activity in those with advanced HIV. Future trials comparing fosamprenavir with current standard regimens will further assist in defining its role in clinical practice.

摘要

福沙那韦是安普那韦的前药制剂,是一种蛋白酶抑制剂,最近在美国被批准用于治疗HIV感染。该药物将安普那韦的药理学特性与低药片负担和灵活的给药方案相结合。三项大型国际试验已经完成。在初治患者中,福沙那韦(无论是否与利托那韦联用)在与奈非那韦对比时达到了非劣效性的主要终点。在初治患者中,接受福沙那韦与利托那韦联用方案治疗失败的患者未出现蛋白酶抑制剂突变。在经治患者中,将福沙那韦与利托那韦联用方案与洛匹那韦/利托那韦进行了对比。未达到非劣效性,但当福沙那韦每日给药两次时,实现病毒抑制的患者数量相近。福沙那韦在初治患者中显示出良好的血脂情况,且不良反应发生率较低。与洛匹那韦/利托那韦一样,福沙那韦在晚期HIV患者中具有强大活性,这使其在其他蛋白酶抑制剂中脱颖而出。未来将福沙那韦与当前标准方案进行对比的试验将进一步有助于明确其在临床实践中的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验