The purpose of this study is to see if it is safe and effective to give adefovir dipivoxil plus abacavir (ABC) plus efavirenz (EFV) plus amprenavir (APV) to HIV-infected patients who have failed to respond to previous treatment with protease inhibitors (PIs).
Patients receive a treatment regimen of adefovir dipivoxil, abacavir, efavirenz, and amprenavir for 24 weeks. During the study, patients are evaluated for changes from baseline in plasma HIV-1 RNA levels and lymphocyte subsets and for development of adverse events and toxicities. Patients who experience virologic failure are discontinued from the study. After Week 24, patients with documented virologic response are eligible to continue receiving the study treatment and to attend scheduled follow-up visits.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Enrollment
25
Pacific Oaks Med Group
Beverly Hills, California, United States
Univ of Colorado / Health Science Ctr
Denver, Colorado, United States
AIDS Research Consortium of Atlanta
Atlanta, Georgia, United States
Brown Univ School of Medicine
Providence, Rhode Island, United States
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Hampton Roads Med Specialists
Hampton, Virginia, United States