首页> 外文期刊>Current opinion in HIV and AIDS >Dolutegravir–rilpivirine coformulation
【24h】

Dolutegravir–rilpivirine coformulation

机译:Dolutegravir-rilpivirine Coformulation

获取原文
获取原文并翻译 | 示例
       

摘要

Purpose of review With prolonged life expectancy in HIV-positive patients on combination antiretroviral therapy, the quest for reducing lifelong drug exposure and minimizing or avoiding the toxicities of combination antiretroviral therapy while maintaining viral suppression has emerged when coformulations of antiretroviral agents with improved convenience, and better tolerability and efficacy became available. This review aims to update the current experience with the novel two-drug combination of dolutegravir (DTG) and rilpivirine (RPV) and elucidate the possible applications and limitations of coformulated DTG–RPV in the future. Recent findings Five observational studies and two randomized, noninferiority trials (SWORD-1 and SWORD-2) evaluated the use of DTG and RPV in treatment-experienced patients. Despite variable inclusion criteria, 95–100% of the included patients maintained plasma HIV RNA load less than 50 copies/ml at the end of 24–48 weeks of observation. Overall, this regimen was well tolerated and only 0.8–7.9% of the patients discontinued the regimen due to adverse events. Summary DTG and RPV is a novel two-drug antiretroviral combination regimen that can be effectively and safely used in patients with viral suppression for 6 months or longer. However, its use in patients with a previous history of virological failure and/or antiretroviral resistance warrants further investigation.
机译:在艾滋病毒阳性患者中延长预期率的审查目的,试验终身药物暴露和最小化或避免组合抗逆转录病毒治疗的毒性,同时在抗逆转录病毒改善方便性的抗逆转录病毒剂的过程中出现了在保持病毒抑制的同时,更好的耐受性和有效性可用。该审查旨在更新目前的多鲁尔(DTG)和瑞培(RPV)的新型双药物组合的经验,并阐明了未来Coformulated DTG-RPV的可能应用和局限性。最近的发现五个观察性研究和两项随机性非事故试验(Sword-1和Sword-2)评估了DTG和RPV在治疗经验丰富的患者中的使用。尽管具有可变的含有标准,但在24-48周的观察结束时,95-100%的含量患者维持血浆HIV RNA负载小于50拷贝/ mL。总体而言,这种方案耐受性良好,只有0.8-7.9%的患者因不良事件而停止了方案。发明内容DTG和RPV是一种新型的两种药物抗逆转录病毒组合方案,可以有效和安全地用于病毒抑制6个月或更长时间的患者。然而,它用于以前的病毒学失败和/或抗逆转录病毒阻力历史的患者进一步调查。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号