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Clinical Trial Summary

The purpose of this study was to evaluate the efficacy of GSK3640254 + DTG relative to lamivudine (3TC) + DTG in treatment-naïve adult participants living with human immunodeficiency virus (HIV)-1. The participants were randomized to one of the three doses of blinded GSK3640254 (100, 150, or 200 milligrams [mgs]) or a reference arm of blinded 3TC-each in combination with open label DTG.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04900038
Study type Interventional
Source ViiV Healthcare
Contact
Status Terminated
Phase Phase 2
Start date August 18, 2021
Completion date May 11, 2023

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