drugset / Trial / NCT05489406

Relative Bioavailability Study to Investigate a Potential Interaction Between DTG DT and F/TAF TOS.

NCT05489406

RandomizedCrossoverOpen-labelOther

Summary

This relative bioavailability (RBA) study will be conducted to investigate whether there is a potential pharmacokinetic effect when paediatric DTG and F/TAF are taken together as dispersible formulations. This study will be performed in healthy volunteers instead of HIV-infected patients.

Timeline

Start
2022-10-06
Primary completion
2023-03-24
Completion
2023-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Dolutegravir Other / unclassified 30 mg Oral
Subject emtricitabine Other / unclassified 180 mg Oral
Subject tenofovir alafenamide Small molecule 22.5 mg Oral