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NCT02369406Active, not recruitingPhase 2/3

Early Infant HIV Treatment in Botswana

BHP Early Infant Treatment Study: A Clinical Treatment Trial of HIV+ Infants in Botswana

Source: ClinicalTrials.gov · Last updated 23 Feb 2026

Brief summary (registry, in English)

The overall objective of this study is to determine whether very early antiretroviral treatment (ART) initiation in HIV-infected infants limits the seeding of viral reservoirs and maintains immune responses, potentially allowing future periods off ART.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
67 (actual)
First submitted
12 Feb 2015
Start date
4 May 2015
Primary completion date
6 Nov 2020
Lead sponsor
Harvard School of Public Health (HSPH)
Diseases
HIV
NCT number
NCT02369406

What you commit to

  • Study type: Interventional · Phase 2/3
  • Participants enrolled: 67
  • From 4 May 2015 to the primary completion date, 6 Nov 2020
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Hospitalization for life-threatening medical illness
  • Medical condition making it unlikely that the infant will survive to 96 weeks

Lab values

  • If lab values are available prior to enrollment, the following Division of AIDS 2014 graded results, from samples collected within 7 days prior to entry without subsequent testing, will exclude an infant:
    • Grade ≥3 ALT
    • Grade ≥3 AST
    • Grade ≥4 hemoglobin
    • Note: Baseline lab values may not be available at the time of ART start. However, as soon as these values are available (occasionally within \<24 hours), they will be used to make rapid treatment decisions. Neonates with baseline Grade 4 hemoglobin will be called immediately to have ZDV discontinued if the value is confirmed. Neonates with baseline Grade 3 or 4 ALT or AST will be called immediately to stop either NVP or LPV/r if the value is confirmed. Neonates who remain on ART may remain on study. Neonates who discontinue all ART for pre-ART laboratory abnormalities will not be counted against total enrollments.

Other

  • 1\) \< 85% reported adherence to prescribed doses or interruption of ART for more than 7 consecutive days since its initiation.

Who the study is looking for

  • Mother/guardian ≥18 years of age and able to provide informed consent
  • Gestational age at birth ≥35 weeks
  • Birth weight ≥2000 grams
  • Age is less than 7 days\*
  • HIV-infection identified by testing conducted within 96 hours after birth NOTE: HIV-infection is defined as DNA PCR positive on at least one specimen, with confirmation specimen either positive or pending\*\*
  • Ability to initiate ART within 7 days after birth
  • Eligible for ART through the Botswana government program
  • Ability to be followed in BHP clinic for up to 240 weeks from enrollment#
  • Blood samples collected and submitted for real-time safety lab evaluations; results may be pending at the time of entry.
    • At least half of infants in the antepartum cohort must be \< 3 days at enrollment, including 3 of the first 6 infants enrolled.
    • Participants will be offered extended follow-up for up to 576 weeks. However, willingness to participate in optional extended follow-up is not an inclusion criterion.
  • Mother/guardian ≥18 years of age and able to provide informed consent
  • Age is greater than 4 days and less than 57 days
  • HIV-negative within 96 hours after birth NOTE: HIV-negative is defined as HIV-negative by DNA PCR on a single specimen or HIV-negative on 2 separate confirmatory specimens following a re-test of an HIV-positive sample
  • HIV-positive between 96 hours and 56 days after birth NOTE: DNA PCR positive on at least one specimen with confirmation specimen either positive or pending repeat draw or result\*\*
  • Ability to initiate ART at enrollment
  • Eligible for ART through the Botswana government program
  • Ability to be followed in BHP clinic for ART for up to 240 weeks after enrollment#
  • Blood samples collected and submitted for real-time safety lab evaluations (results may be pending at the time of entry).
    • An enrolled infant later determined to be HIV uninfected by confirmatory testing will end participation in the study and this enrollment will not be counted against the total number of enrollments planned.
    • Participants will be offered extended follow-up for up to 576 weeks. However, willingness to participate in optional extended follow-up is not an inclusion criterion.
  • Mother/guardian ≥18 years of age and able to provide informed consent
  • 24-36 months of age
  • HIV-infection documented within 365 days after birth
  • ART initiated within the following timeframe based on timing of HIV-infection diagnosis \> 30-365 days after birth if HIV-infection diagnosed within 96 hours after birth OR \> 57-365 days after birth if infant was HIV-negative based on testing performed within 96 hours after birth (or if unknown HIV status \< 96 hours from birth) and then found to be HIV-positive based on testing performed between 96 hours and 365 days after birth.
  • After 6 months of ART, no more than one HIV RNA measurement \> 400 copies/mL

Age in the registry: 0 days to 3 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Botswana Harvard HIV/AIDS Institute Partnership
Coordinator of this site? Confirm its status
GaboroneBotswanaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.