Summary

Location
at San Diego, California and other locations
Dates
study started
completion around
Principal Investigator
by Stephen Spector, MD

Description

Summary

IMPAACT 2028 is an observational prospective study to characterize a cohort of early treated children who may participate in future research related to HIV remission or cure. Up to approximately 250 participants will be in the study for approximately seven years. No intervention is provided in the study.

Details

This is an observational prospective cohort study characterizing and establishing a biorepository of early treated children who may participate in future research related to HIV remission or cure. Early treatment is defined as treatment with at least three ARV agents from at least two classes of ART initiated within 12 weeks of birth. Within the overall study population, for descriptive and analysis purposes, children who initiated treatment within 48 hours of birth will be classified as having received very early treatment. A subset of children will have received bNAbs as part of their treatment regimens.

Up to approximately 250 children living with HIV who received early treatment in IMPAACT network studies or other research studies sponsored by the US National Institutes of Health (NIH) will be enrolled and followed semi-annually for up to seven years. Clinical, virologic, and immunologic evaluations will be performed semi-annually at each study visit, and specimens will be collected for the study's biorepository for future investigations.

Keywords

HIV Infection, HIV Infections, Cohort 1

Eligibility

You can join if…

  • Participated in one of the parent studies
  • Confirmed HIV-1 infection based on documented nucleic acid testing of two blood samples collected at different time points
  • Received early treatment for HIV-1 infection, defined as treatment with at least three ARV agents from at least two classes of ART, initiated within 12 weeks of birth
  • Based on parent or guardian report at entry, child is expected to be available for at least 24 months of follow-up
  • Parent or guardian is willing and able to provide written informed consent for child's study participation and, when applicable per institutional review board/ethics committee (IRB/EC) policies and procedures, child is willing and able to provide written assent for study participation

You CAN'T join if...

  • Has any documented or suspected clinically significant medical condition or any other condition that, in the opinion of the site investigator, would make participation in the study unsafe or otherwise interfere with completing study procedures

Locations

  • University California, San Diego (CRS 4601) accepting new patients
    San Diego California 92103 United States
  • David Geffen School of Medicine at UCLA (CRS 5112) accepting new patients
    Los Angeles California 90095 United States

Lead Scientist at UCSD

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
ID
NCT05154513
Study Type
Observational
Participants
Expecting 250 study participants
Last Updated