Abstract
Purpose: Fosamprenavir/ritonavir 1400 mg/100 mg once-daily regimen may have a more favourable tolerability and lipid profile than the fosamprenavir/ ritonavir twice-daily regimen, while maintaining comparable antiviral efficacy. Methods: This open-label study had a group-sequential design with a stage 1 Week 24 futility analysis, with both efficacy and safety go-criteria for progression to stage 2. There were 214 antiretroviral-naive, HIV-1-infected subjects who were randomised to receive either fosamprenavir/ritonavir 1400 mg/100 mg once daily or fosamprenavir/ ritonavir 700 mg/100 mg twice daily, both with abacavir/lamivudine fixed-dose combination tablet. Primary endpoints were the proportion of subjects achieving HIV-1 RNA
Original language | English |
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Pages (from-to) | 356-367 |
Number of pages | 12 |
Journal | HIV Clinical Trials |
Volume | 10 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jan 1 2009 |
Keywords
- Abacavir
- Fosamprenavir
- HIV
- Ritonavir
ASJC Scopus subject areas
- Infectious Diseases
- Pharmacology (medical)