drugset / Trial / NCT00428116

Summary

Given the high mortality associated with infant HIV-1 and the fact that surrogate markers are poorly predictive of mortality risk,empiric highly active antiretroviral therapy (HAART) initiation is started in infants younger than 12 months. A problem with this approach is that it obligates infants to life-long therapy, which may be associated with cumulative drug toxicity, poor adherence, and treatment failure. Early HAART for prevention of mortality during the first 2 years of life has potential to salvage immune function and alter viral set-point, allowing withdrawal of therapy, perhaps for several years, until subsequent CD4% decline requires it. This untested approach is attractive because it combines the survival benefits of early pediatric HAART therapy with the benefits of antiretroviral deferral. One hundred and fifty infants who initiated HAART at \<13 months of age will be treated with HAART regimen for 24 months after which those who have immune reconstitution and adequate growth (\~100) will be randomized to continued versus deferred therapy. Clinical outcomes, growth, and toxicity will be compared in these children to determine if interruption is a safe and beneficial strategy. Follow-up in this studies will be closely monitored by an external Data Safety and Monitoring Board (DSMB).

Timeline

Start
2007-09
Primary completion
2013-07
Completion
2014-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abacavir Other / unclassified
Comparator Didanosine Small molecule
Comparator Lamivudine Other / unclassified
Comparator Nevirapine Small molecule
Comparator Ritonavir Other / unclassified
Comparator Stavudine Other / unclassified
Comparator Zidovudine Small molecule