The purpose of this study is to evaluate 1) the safety and tolerance of longterm triple therapy combinations of DLV, ZDV, and ddC, or DLV, ZDV, and ddI in HIV-1 individuals who were particants in previous protocols; 2) the efficacy of the triple therapy regimen based on changes in CD4 counts, plasma HIV-1 RNA by PCR, and on time to disease progression or death, 3) the clinical efficacy of the triple therapy regimen; and 4) to continue to follow patients from an earli study with delavirdine mesylate for pharmacoeconomic activities.
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