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Study identifier: NCT05069688 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Dolutegravir Pharmacokinetics Among HIV/TB Coinfected Children Receiving Standard and High-dose Rifampicin

Condition: Pediatric HIV Infection · Tuberculosis Infection  ·  Sponsor: Brigham and Women's Hospital

PhasePhase 1
Planned participants20
Who can joinAll sexes, 4 Weeks to 5 Years
Healthy volunteersNo

About this study

Tuberculosis (TB) is the leading cause of death among children with HIV, yet insufficient data are available on the pharmacokinetics of newer HIV/TB cotreatment strategies in children. Current WHO-recommended rifampicin dosages result in low concentrations in most children, and high-dose rifampicin may improve outcomes and shorten treatment duration. Yet the impact of high-dose rifampicin on dolutegravir exposures has not been examined in children. This study aims to evaluate the safety and pharmacokinetics of dolutegravir twice daily among HIV/TB coinfected children receiving standard-dose and high-dose rifampicin.

This description comes directly from the study's public registry record.

Talk to the study team

Holly Rawizza, MD, MPH  ·  617-432-4686  ·  hrawizza@bwh.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University College Hospital/ University of IbadanIbadan, Oyo State, NigeriaRecruiting

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Source record: clinicaltrials.gov/study/NCT05069688