This study is a 48-week study to evaluate the efficacy and safety of an investigational regimen combining FDA approved HIV drugs in antiretroviral-experienced subjects failing on their first highly active antiretroviral therapy regimen.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
GSK Investigational Site
HIV viral load response at 48 weeks as measured by proportion of subjects with undetectable viral load.
Time frame: 48 weeks
Safety Viral load response at 24 weeks Change in T-cell count Resistance Health outcomes
Time frame: 24 weeks
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Los Angeles, California, United States
GSK Investigational Site
San Rafael, California, United States
GSK Investigational Site
Fort Lauderdale, Florida, United States
GSK Investigational Site
Jacksonville, Florida, United States
GSK Investigational Site
Lake Worth, Florida, United States
GSK Investigational Site
Miami, Florida, United States
GSK Investigational Site
Miami Beach, Florida, United States
GSK Investigational Site
North Miami, Florida, United States
GSK Investigational Site
Orlando, Florida, United States
GSK Investigational Site
Tallahassee, Florida, United States
...and 17 more locations