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Study ID

APV102002

Study Title A Phase III, Randomized, Controlled, Open-label, Multicentre, Three Arm Study to Compare the Efficacy and Safety of a Dual-boosted HIV-1 Protease Inhibitor regimen of Fosamprenavir/Lopinavir/Ritonavir 1400mg/533mg/133mg Twice Daily and an Increased Dosage Regimen of FPV/RTV 1400mg/100mg BID Versus the Standard Dosage Regimen of FPV/RTV 700mg/100mg BID for 24 Weeks in Multiple-PI Experienced, HIV-infected Adults Experiencing Virological Failure
Clinicaltrials.gov Identifier NCT00144833
Sponsor GlaxoSmithKline
Collaborators N/A
Study Recruitment Status Completed
Generic Name fosamprenavir
Trade Name Telzir,Telzer,Lexiva
Study Indication Infection, Human Immunodeficiency Virus