Indinavir is usually taken three times a day. The purpose of this study is to see if it is safe and effective to take indinavir only twice a day plus nelfinavir (also taken twice a day) and efavirenz (taken once a day).
Patients receive a treatment regimen consisting of nelfinavir, indinavir, and efavirenz for 48 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. After Week 48, patients with documented virologic response are eligible to continue receiving study treatments and to attend scheduled follow-up visits. Patients who experience virologic failure are discontinued from the study.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
NONE
Enrollment
6
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