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Clinical Trial Summary

The primary objective of this study is to evaluate the steady state PK of bictegravir (BIC) and confirm the dose of BIC/emtricitabine/tenofovir alafenamide (B/F/TAF) 50/200/25 mg fixed dose combination (FDC) in HIV-1 infected, virologically suppressed pregnant women in their second and third trimesters.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03960645
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 1
Start date June 28, 2019
Completion date August 18, 2022

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