The purpose of this study is to study amprenavir/ritonavir, saquinavir/ritonavir or efavirenz in HIV-infected patients following failure with Kaletra (ABT-378/ritonavir) as their first protease inhibitor based HAART.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Proportion of subjects with plasma HIV RNA levels below the limit of quantification (400 copies/mL) at week 24 and the time until loss of virologic response through week 48
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Phoenix Body Positive, Inc.
Phoenix, Arizona, United States
Paul J. Cimoch, M.D.
Fountain Valley, California, United States
AIDS Health Care Foundation - Research Center
Los Angeles, California, United States
Tower Infectious Diseases Medical Associates
Los Angeles, California, United States
20th Avenue Medical Center Kaiser Permanente
Denver, Colorado, United States
University of Colorado Health Sciences Center
Denver, Colorado, United States
IDC Research Initiative
Altamonte Springs, Florida, United States
Gary J. Richmond, M.D.
Fort Lauderdale, Florida, United States
Associates in Research
Fort Myers, Florida, United States
University of Miami School of Medicine
Miami, Florida, United States
...and 44 more locations