Efficacy and safety of delavirdine mesylate with zidovudine and didanosinecompared with two-drug combinations of these agents in persons with HIV disease with CD4 counts of 100 to 500 cells/mm(3) (ACTG 261)

To evaluate the antiretroviral activity of delavirdine mesylate, a nonnucle oside reverse transcriptase inhibitor of HIV-1, we performed a phase II, ra ndomized, double-blind, multicenter trial comparing the three-drug combinat ion of delavirdine with zidovudine and didanosine to two-drug combinations of these drugs. Patients with CD4 cell counts between 100 and 500 cells/mm( 3) without prior or <6 months of monotherapy with zidovudine or didanosine were randomized to one of four arms and observed on a follow-up basis for 4 8 weeks. In total, 544 patients were evaluated. In those assigned to the th ree-drug regimen, mean short-term (weeks 4-12) and long-term (weeks 40-48) change in CD4 cells from baseline were 49.3 +/- 8.1 and 65.4 +/- 13.4 cells /mm(3), respectively; mean short-term and long-term HIV-1 RNA changes from baseline were -1.13 log(10) +/- 0.12 and -0.73 +/- 0.12 copies/ml, respecti vely. These responses in CD4 cell counts and HIV-1 RNA levels were better i n comparisons with each of the two-drug arms at all study points; however, differences were not consistently significant. Gastrointestinal side effect s were experienced by 33% of patients (178 of 544), and 30% (121 of 407) re ceiving delavirdine experienced rash, only one case of which was severe. In this study, therapy with delavirdine + zidovudine + didanosine was safe an d showed modest, but not always significant, antiviral activity and CD4 cel l count benefit compared with two-drug regimens with these agents.