TB Research

Pharmacokinetics of Efavirenz 600mg in Combination with Rifampicin in Chinese HIV/TB Co-Infection Patients

Tongtong Wang, Yingchu Liu, Zhu Chunyu, Siyuan Yang, Di Yang, Xiao Jiang, Guiju Gao

Infection and Drug Resistance · 2023-07

Abstract

Background: Rifampicin is a known inducer of the cytochrome P450 (CYP2B6) enzyme, which can lead to a decrease in the concentration of efavirenz. Therefore, we conducted a study to evaluate the effect of daily rifampicin intake on efavirenz 600mg pharmacokinetics and HIV-1 virological suppression. Methods: Patients receiving antiretroviral therapy containing efavirenz (600mg daily), and we collected efavirenz concentration at four visit points: ART day 14 (PK1), ART day 42 (PK2), ART day 140 (PK3), and ART day 336 (PK4), and performed pharmacokinetics analysis. Results: From February 2017 to November 2020, 29 HIV/TB co-infection patients were included. Ninety percent of patients had a concentration of ≥ 1000ng/mL of efavirenz during the study. All patients had efavirenz C max ≥ 1000ng/mL, 86% patients showed good virology response. Conclusion: Our study shows that the use of rifampicin in HIV/TB co-infection patients does not affect efavirenz drug concentrations, that virological suppression is good and that no efavirenz dose adjustment is required. Keywords: HIV/TB, rifampicin, efavirenz, pharmacokinetics

MeSH terms

  • Efavirenz
  • Human immunodeficiency virus (HIV)
  • Pharmacokinetics
  • Medicine
  • Pharmacology
  • Rifampicin
  • Antiretroviral therapy