The purpose of this study is to compare the anti-HIV efficacy, safety and effect of serum lipids of two boosted protease inhibitor-based HAART regimens (ARV/RTV v. LPV/RTV) in HIV-1 infected subjects who have experienced their first virologic failure while receiving a NNRTI-containing HAART regimen.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
Capsules, Oral, 300mg/100mg, once daily, 24 weeks.
Capsules, Oral, 800mg/200mg, twice daily, 24 weeks.
Co-Primary Outcomes in this study 1)Viral load reduction from baseline through Week 24 2)Change in lipids from baseline at Week 12
Viral load reduction from baseline at Weeks 48,72,96;Subjects with HIV RNA<50 and <400 c/mL at Weeks 24,48,72 & 96;Patterns of resistance;Safety and tolerability through Week 96 including fasting lipid values;Adherence at Weeks 4,12,24,48,72 & 96.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Local Institution
Hobson City, Alabama, United States
Local Institution
Montgomery, Alabama, United States
Local Institution
Phoenix, Arizona, United States
Local Institution
Little Rock, Arkansas, United States
Local Institution
Bakersfield, California, United States
Local Institution
Los Angeles, California, United States
Local Institution
San Francisco, California, United States
Local Institution
San Mateo, California, United States
Local Institution
Tarzana, California, United States
Local Institution
West Hollywood, California, United States
...and 43 more locations