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Pharmacokinetics of rilpivirine and 24-week outcomes after switching from efavirenz in virologically suppressed HIV-1-infected adolescents.
Antiviral Therapy ( IF 1.2 ) Pub Date : 2017-10-11 , DOI: 10.3851/imp3198
Watsamon Jantarabenjakul 1, 2 , Suvaporn Anugulruengkitt 1, 2 , Naruporn Kasipong 3 , Narukjaporn Thammajaruk 3 , Jiratchaya Sophonphan 3 , Torsak Bunupuradah 2, 3 , Tim R Cressey 4, 5, 6 , Angela Colbers 7 , David M Burger 7 , Wanatpreeya Phongsamart 8 , Thanyawee Puthanakit 1, 2 , Chitsanu Pancharoen 1, 2 ,
Affiliation  

Rilpivirine (RPV), a non-nucleoside reverse transcriptase inhibitor drug, could be a favourable drug for maintenance therapy in HIV-infected adolescents because it has few long-term side effects. However, data among adolescents switching from efavirenz (EFV) to RPV are limited. This study investigated the pharmacokinetics (PK), safety and efficacy of RPV in virologically suppressed HIV-1-infected adolescents after switching from EFV.

中文翻译:

在病毒学抑制的HIV-1感染青少年中,从依非韦伦转换后,利匹韦林的药代动力学和24周结果。

Rilpivirine(RPV)是一种非核苷类逆转录酶抑制剂药物,因为它几乎没有长期副作用,因此可能是用于HIV感染青少年维持治疗的理想药物。但是,从依非韦伦(EFV)转换为RPV的青少年中的数据有限。这项研究调查了从EFV切换后,病毒性抑制HIV-1感染的青少年中RPV的药代动力学(PK),安全性和有效性。
更新日期:2020-08-21
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