192
Participants
Start Date
January 31, 2004
Primary Completion Date
May 31, 2006
Study Completion Date
May 31, 2006
atazanavir/ritonavir +2 NRTIs (immediate Switch Group)
Capsules, Oral, ATV 300mg/RTV 100mg + 2 NRTIs, QD, 48 weeks.
LPV/r +2 NRTIs (Delayed/optional Switch Group)
Capsules, Oral, LPV 400mg/RTV 100mg +2 NRTIs, BID, 24 weeks then option to switch to ATV arm or stay until 48 weeks.
Local Institution, Phoenix
Local Institution, Bakersfield
Local Institution, Los Angeles
Local Institution, San Francisco
Local Institution, Miami
Local Institution, Boston
Local Institution, New York
Local Institution, Cincinnati
Local Institution, Portland
Local Institution, Philadelphia
Local Institution, Columbia
Local Institution, Dallas
Local Institution, Hamilton
Local Institution, Montreal
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY