HIV Infections Clinical Trial
Official title:
A Randomized Comparative Study of Combined Zidovudine-Lamivudine (3TC) vs. the Better of ddI Monotherapy vs. Zidovudine Plus Ddl in Symptomatic HIV-1 Infected Children
To compare the efficacy of lamivudine (3TC) and zidovudine (AZT) in combination versus the
better of didanosine (ddI) monotherapy or ddI/AZT combination, in symptomatic HIV-1 infected
children who received less than 56 days of prior antiretroviral therapy. To evaluate the
safety and tolerance of 3TC/AZT in this patient population. To determine other measures of
diseases in response to the study regimens.
Currently, none of the potential treatments for HIV-1 infection has proven to be both
nontoxic and effective in long-term use. However, previous studies in both adults and
children have shown that 3TC combined with AZT reduced HIV load in blood and increased white
blood cells. Additionally, 3TC has demonstrated a favorable safety profile.
Currently, none of the potential treatments for HIV-1 infection has proven to be both
nontoxic and effective in long-term use. However, previous studies in both adults and
children have shown that 3TC combined with AZT reduced HIV load in blood and increased white
blood cells. Additionally, 3TC has demonstrated a favorable safety profile.
Patients are randomized to receive oral 3TC/AZT, ddI/AZT, or ddI alone for at least 24
months. PER AMENDMENT 4/29/96: NOTE: Randomization to ZDV+ddI arm was terminated in Spring
of 1996 based upon the results of ACTG 152. Patients on that arm will continue on blinded
study drug and will be followed until the end of the study.
;
Endpoint Classification: Safety Study, Masking: Double-Blind, Primary Purpose: Treatment
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