Study of Boosted Atazanavir (ATV) Versus Non-boosted ATV in Naive Patients
HIV Infections

About this trial
This is an interventional treatment trial for HIV Infections focused on measuring HIV, Treatment Naive
Eligibility Criteria
Inclusion Criteria: Signed Informed Consent HIV RNA greater than or equal 200 copies/mL at screening 18 years old or older Must use barrier contraception Women of child-bearing potential must have a negative serum or urine pregnancy test within 72 hours before beginning to take the study medications Exclusion Criteria: Unable or unwilling to use acceptable method of birth control for the entire study period including 8 weeks after the study Women using oral contraceptives, pregnant or breastfeeding women Women who have a positive pregnancy test on enrollment or before beginning to take the study medications People who have a life expectancy of greater than 12 months Newly diagnosed HIV-related OI or any medical condition requiring acute therapy at the time of enrollment Any antiretroviral therapy within 30 days prior to screening Any prior antiretroviral therapy (greater than 30 days of NRTI and/or greater than 7 days of non-nucleoside reverse-transcriptase inhibitor (NNRTI) or protease inhibitor therapies) Any of the following conditions: Cushings Syndrome, Gilbert's Syndrome, untreated hypothyroidism or hyperthyroidism, suspected primary (acute) HIV infection, obstructive liver disease, proven or suspected acute hepatitis in the 30 days prior to study entry, Intractable diarrhea (at greater than 6 loose stools per day for at least 78 consecutive days) within 30 days prior to study entry, history of hemophilia, history of acute or chronic pancreatitis, presence of cardiomyopathy (due to any cause) or any significant cardiovascular disease, such as unstable ischemic heart disease Active alcohol or substance abuse History or signs and symptoms of bilateral peripheral neuropathy greater than grade 2 at the time of screening Previous therapy with myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic, or cytotoxic potential within 3 months of study start or the expected need for such therapy or therapy with methadone or ribavirin/interferons or treatment with neurotoxic drugs or drugs that affect CYP3A4 Inability to swallow capsules
Sites / Locations
- Various locations within the US
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
1
2