252
Participants
Start Date
November 30, 2005
Primary Completion Date
August 31, 2007
Study Completion Date
January 31, 2008
Atazanavir + 2 NRTIs
Capsules, tablets, Oral, 48 weeks (after a 26-to-30-week induction phase with ATV 300 mg + RTV 100 mg + 2 NRTIs)
Atazanavir + Ritonavir + 2 NRTIs
Capsules, tablets, Oral, 48 weeks (after a 26-to-30-week induction phase with ATV 300 mg + RTV 100 mg + 2 NRTIs)
Local Institution, Tallinn
Local Institution, Le Kremlin-Bicêtre
Local Institution, Orléans
Local Institution, Paris
Local Institution, Suresnes
Local Institution, Düsseldorf
Local Institution, Hanover
Local Institution, Stuttgart
Local Institution, Ulm
Local Institution, Dublin
Local Institution, Brescia
Local Institution, Milan
Local Institution, Napoli
Local Institution, Padua
Local Institution, Riga
Local Institution, Cascais
Local Institution, Porto
Local Institution, Moscow
Local Institution, Saint Petersburg
Local Institution, Smolensk
Local Institution, Elche
Local Institution, Barcelona
Local Institution, Madrid
Local Institution, Valencia
Local Institution, Bristol
Local Institution, Edinburgh
Local Institution, London
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY