Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treated with zidovudine 200 mg 3 times a day, lamivudine 150 mg 2 times a day, and indinavir 800 mg 3 times a day for 1 year. From a mean pretreatment viral RNA level of 4.93 log10 copies/mL, the proportions of patients having <500 copies/mL at 24 and 52 weeks were 92.0% and 89.2%, respectively. For the 35 patients with data available at 24 and 52 weeks, the corresponding proportions for the <50 copies/mL analysis were 86.6% and 79.3%, respectively. The change in virus load was −2.19 and −2.41 log10 copies/mL at weeks 8 and 52, respectively. CD4 cell counts increased, from a mean of 546 cells/mm3, by 142 cells/mm3 at week 24 and by 210 cells/mm3 a...
Objective: To evaluate the clinical, immunologic, and virologic response to indinavir, zidovudine, a...
Objective. - To compare the safety and efficacy of 2 doses of lamivudine given in combination with z...
BACKGROUND: The efficacy and safety of adding a protease inhibitor to two nucleoside analogues to tr...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Background: The new protease inhibitors are potent inhibitors of the human immunodeficiency virus (H...
A randomized, double-blind, multicenter study of indinavir, zidovudine, and lamivudine was conducted...
Background. The reverse-transcriptase inhibitor lamivudine has in vitro synergy with zidovudine agai...
Clinical benefit of zidovudine alone in the treatment of HIV infection wanes after several years, wi...
The objective of this study was to determine the efficacy and safety of adding zidovudine to continu...
Background: The efficacy and safety of adding a protease inhibitor to two nucleoside analogues to tr...
A double-blind, randomized study of zidovudine-experienced, PI- and lamivudine-naive adults with bas...
OBJECTIVE: To assess the durability of the antiretroviral effect in plasma and cerebrospinal fluid (...
A multicenter, double-blind, placebo-controlled trial randomized 28 patients with primary (acute) hu...
Objective: To evaluate the clinical, immunologic, and virologic response to indinavir, zidovudine, a...
Objective. - To compare the safety and efficacy of 2 doses of lamivudine given in combination with z...
BACKGROUND: The efficacy and safety of adding a protease inhibitor to two nucleoside analogues to tr...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Forty-seven patients presenting with primary human immunodeficiency virus (HIV) infection were treat...
Background: The new protease inhibitors are potent inhibitors of the human immunodeficiency virus (H...
A randomized, double-blind, multicenter study of indinavir, zidovudine, and lamivudine was conducted...
Background. The reverse-transcriptase inhibitor lamivudine has in vitro synergy with zidovudine agai...
Clinical benefit of zidovudine alone in the treatment of HIV infection wanes after several years, wi...
The objective of this study was to determine the efficacy and safety of adding zidovudine to continu...
Background: The efficacy and safety of adding a protease inhibitor to two nucleoside analogues to tr...
A double-blind, randomized study of zidovudine-experienced, PI- and lamivudine-naive adults with bas...
OBJECTIVE: To assess the durability of the antiretroviral effect in plasma and cerebrospinal fluid (...
A multicenter, double-blind, placebo-controlled trial randomized 28 patients with primary (acute) hu...
Objective: To evaluate the clinical, immunologic, and virologic response to indinavir, zidovudine, a...
Objective. - To compare the safety and efficacy of 2 doses of lamivudine given in combination with z...
BACKGROUND: The efficacy and safety of adding a protease inhibitor to two nucleoside analogues to tr...