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Pharmacokinetics and Safety of a Raltegravir-Containing Regimen in Children Aged 4 Weeks to 2 Years Living With Human Immunodeficiency Virus and Receiving Rifampin for Tuberculosis.
Journal of the Pediatric Infectious Diseases Society ( IF 2.5 ) Pub Date : 2020-05-25 , DOI: 10.1093/jpids/piaa039
Paul Krogstad 1 , Pearl Samson 2 , Edward P Acosta 3 , Jack Moye 4 , Ellen Townley 5 , Sarah Bradford 6 , Emily Brown 6 , Kayla Denson 7 , Bobbie Graham 7 , Laura Hovind 7 , Thucuma Sise 5 , Hedy Teppler 8 , Sisinyana Ruth Mathiba 9 , Lee Fairlie 10 , Jana L Winckler 11 , Gretchen Slade 12 , Tammy Meyers 13 ,
Affiliation  

Pharmacological interactions limit treatment options for children living with human immunodeficiency virus (HIV) and tuberculosis (TB). We found that 12 mg/kg twice daily raltegravir chewable tablets (administered after crushing) safely achieved pharmacokinetic targets in children living with HIV aged 4 weeks to <2 years receiving concurrent rifampin to treat TB. CLINICAL TRIALS REGISTRATION NCT01751568.

中文翻译:


含有拉替拉韦的治疗方案在感染人类免疫缺陷病毒并接受利福平治疗结核病的 4 周至 2 岁儿童中的药代动力学和安全性。



药理学相互作用限制了感染人类免疫缺陷病毒 (HIV) 和结核病 (TB) 的儿童的治疗选择。我们发现,12 mg/kg 每日两次的拉替拉韦咀嚼片(压碎后给药)在 4 周至 2 岁以下同时接受利福平治疗结核病的 HIV 感染儿童中安全地达到了药代动力学目标。临床试验注册 NCT01751568。
更新日期:2020-05-25
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