Phase IIb, randomized, partially blind, active controlled, dose-range finding study of GSK3640254 compared to a reference arm of dolutegravir, each in combination with nucleoside reverse transcriptase inhibitors, in HIV-1 infected antiretroviral treatment-naive adults.

About this Study

To evaluate antiviral efficacy of GSK3640254 relative to DTG, each given in combination with 2 NRTIs, enabling the selection of an optimal dose for GSK3640254.

Sponsor Protocol ID:208379
IRB Number:2020V0382
Closed for Enrollment
Interventional
Phase 2
Eligibility Criteria
18 years old
Both Male and Female
No
No
No

Inclusion CriteriaParticipants must be 18 years of age inclusive, at the time of signing the informed consent.

 Body weight 50.0 kg (110 lbs.) for men and 45.0 kg (99 lbs) for women and body mass index (BMI) > 18.5 kg/m2 .

A female is eligible to participate if she is not pregnant or breastfeeding.


Exclusion CriteriaPresence of primary HIV-1 infection.


Categories Click category to view its trials.
Infectious Diseases
Participating Locations
University Hospital - UMMC
Contact Information
Contact Name: Malinda McBride
Phone Number: 601-496-9600
Email: mmcbride1@umc.edu
Principal Investigator:Leandro Mena
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