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Atazanavir Versus Lopinavir/Ritonavir (LPV/RTV) in Patients Who Have Not Had Success With Protease Inhibitor-Containing HAART Regimen(s)

Phase 3
Completed
Conditions
HIV Infections
Registration Number
NCT00028301
Lead Sponsor
Bristol-Myers Squibb
Brief Summary

This study will compare 2 treatments in the way they affect cholesterol levels and the amount of HIV in the blood.

Detailed Description

The study is designed to determine the metabolic changes, antiviral activity, safety, and tolerability of atazanavir as compared to LPV/RTV, each in combination with 2 nucleosides, over the initial 24 weeks, with a final analysis at 48 weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (97)

Cooper Green Hosp

🇺🇸

Birmingham, Alabama, United States

Phoenix Body Positive

🇺🇸

Phoenix, Arizona, United States

East Bay AIDS Ctr

🇺🇸

Berkeley, California, United States

Saint Francis Mem Hosp / HIV Care Unit

🇺🇸

San Francisco, California, United States

Kaiser Foundation Hospital

🇺🇸

San Francisco, California, United States

San Francisco Veterans Administration Med Ctr

🇺🇸

San Francisco, California, United States

Harbor UCLA Med Ctr

🇺🇸

Torrance, California, United States

Beacon Clinic / Boulder Community Hosp

🇺🇸

Boulder, Colorado, United States

IDC Research Initiative

🇺🇸

Altamonte Springs, Florida, United States

Larry Bush

🇺🇸

Atlantis, Florida, United States

Scroll for more (87 remaining)
Cooper Green Hosp
🇺🇸Birmingham, Alabama, United States

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