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CompletedNCT00000750Updated Oct 28, 2021

A Phase III Study to Evaluate the Safety, Tolerance, and Efficacy of Early Treatment With Zidovudine (AZT) in Asymptomatic Infants With HIV Infection

A Phase 3 interventional study of Zidovudine in HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Completed at 42 sites in 2 countries. Open to participants aged 1 Day to 9 Months. Per ClinicalTrials.gov, last updated 2021-10-28.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
400
Ages
1 Day to 9 Months
Sex
All
01

Study summary

Primary: To determine the efficacy of early treatment with zidovudine (AZT) in HIV-infected asymptomatic infants. To determine the safety and tolerance of AZT in this patient population.

Secondary: To compare the virologic and immunologic parameters between the treatment groups. To determine the efficacy of AZT as an early treatment to prevent development of CD4+ cell depletion in HIV-infected asymptomatic infants.

AZT is currently indicated for primary treatment in children with HIV-associated signs and symptoms and for those with significant immunodeficiency. This study will attempt to determine whether early treatment with AZT prevents the development of symptoms in HIV-infected infants who are asymptomatic.

Read the detailed description

AZT is currently indicated for primary treatment in children with HIV-associated signs and symptoms and for those with significant immunodeficiency. This study will attempt to determine whether early treatment with AZT prevents the development of symptoms in HIV-infected infants who are asymptomatic.

Patients are randomized to receive oral AZT (at age-adjusted doses) or placebo. Patients are evaluated at weeks 2 and 4 and every 4 weeks thereafter; those who reach a study endpoint will have their treatment unblinded to allow the clinician to determine which treatment regimen the patient should then receive. Patients who meet the criteria for changes to open-label AZT will be given the appropriate age-adjusted dose without unblinding the original randomization assignment. Patients who complete or discontinue treatment are followed every 6 months for up to 2 years.

02

Conditions studied

  • HIV Infections

Keywords

  • Acquired Immunodeficiency Syndrome
  • AIDS-Related Complex
  • Zidovudine
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 400 is above the median of 120 across 4,201 interventional studies indexed under Infections.

Browse Infections studies →

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID) is the lead sponsor of 2,401 studies on the registry; 179 are open to participants now.

Of its 396 completed or terminated interventional studies of FDA-regulated products, 294 (74%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 9 Months
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Patients must have:

  • HIV infection.
  • CD4 count >= 2000 cells/mm3 AND >= 30 percent of total lymphocytes.
  • No signs or symptoms of HIV infection (other than lymphadenopathy, mild hepatomegaly, hypergammaglobulinemia, or splenomegaly, which is permitted).
  • Consent of parent or guardian.

Exclusion criteria

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms and conditions are excluded:

  • Serious acute infection requiring parenteral therapy at time of entry.
  • One or more serious, proven bacterial infections including any of the following:
  • septicemia; pneumonia; meningitis; bone or joint infection; or abscess of an internal organ or body cavity (excluding otitis media or superficial skin or mucosal abscesses) that are caused by Haemophilus, Streptococcus (including pneumococcus), or other pyogenic bacteria.
  • Clinical neurologic/neuropsychologic deficits, or a head circumference less than the fifth percentile.

Concurrent Medication:

Excluded:

  • Any agent with known antiretroviral activity.
  • Acetaminophen, ibuprofen, or aspirin for more than 72 hours continuously.

Prior Medication:

Excluded:

  • More than 7 weeks of prior antiretroviral or immunomodulator therapy post-natally.

Recommended:

  • PCP prophylaxis.
  • Immunizations according to current recommendations.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Enrollment
400 participants

Interventions

  • DrugZidovudine
06

Study locations

42 sites
  • Univ of Alabama at Birmingham Schl of Med / Pediatrics
    Birmingham, Alabama 35294, United States
  • Kaiser Permanente / UCLA Med Ctr
    Downey, California 902422814, United States
  • UCLA Med Ctr / Pediatric
    Los Angeles, California 900951752, United States
  • Harbor - UCLA Med Ctr / UCLA School of Medicine
    Los Angeles, California 905022004, United States
  • San Francisco Gen Hosp
    San Francisco, California 94110, United States
  • UCSF / Moffitt Hosp - Pediatric
    San Francisco, California 941430105, United States
  • Children's Hosp of Denver
    Denver, Colorado 802181088, United States
  • Univ of Connecticut / Farmington
    Farmington, Connecticut 06032, United States
  • Yale Univ Med School
    New Haven, Connecticut 06504, United States
  • Georgetown Univ Med Ctr
    Washington, District of Columbia 20007, United States
  • Children's Hosp of Washington DC
    Washington, District of Columbia 200102916, United States
  • Howard Univ Hosp
    Washington, District of Columbia 20060, United States
  • Univ of Miami (Pediatric)
    Miami, Florida 33161, United States
  • Cook County Hosp
    Chicago, Illinois 60612, United States
  • Univ of Illinois College of Medicine / Pediatrics
    Chicago, Illinois 60612, United States
  • Chicago Children's Memorial Hosp
    Chicago, Illinois 606143394, United States
  • Univ of Chicago Children's Hosp
    Chicago, Illinois 606371470, United States
  • Tulane Univ / Charity Hosp of New Orleans
    New Orleans, Louisiana 701122699, United States
  • Univ of Maryland at Baltimore / Univ Med Ctr
    Baltimore, Maryland 21201, United States
  • Children's Hosp of Boston
    Boston, Massachusetts 021155724, United States
  • Baystate Med Ctr of Springfield
    Springfield, Massachusetts 01199, United States
  • Univ of Massachusetts Med School
    Worcester, Massachusetts 016550001, United States
  • Univ of Medicine & Dentistry of New Jersey / Univ Hosp
    Newark, New Jersey 071032714, United States
  • Children's Hosp of New Jersey / UMDNJ - New Jersey Med Schl
    Newark, New Jersey 071072198, United States
  • Children's Hosp at Albany Med Ctr
    Albany, New York 12208, United States
  • Lincoln Hosp Ctr
    Bronx, New York 10451, United States
  • Bronx Lebanon Hosp Ctr
    Bronx, New York 10457, United States
  • Albert Einstein College of Medicine
    Bronx, New York 10461, United States
  • King's County Hosp Ctr / Pediatrics
    Brooklyn, New York 11203, United States
  • Children's Hosp Pact Prog / Children's Hosp of Buffalo
    Buffalo, New York 14222, United States
  • North Shore Univ Hosp
    Great Neck, New York 11021, United States
  • Metropolitan Hosp Ctr
    New York, New York 10029, United States
  • Mount Sinai Med Ctr / Pediatrics
    New York, New York 10029, United States
  • Harlem Hosp Ctr
    New York, New York 10037, United States
  • Univ of Rochester Medical Center
    Rochester, New York 14642, United States
  • Westchester Hosp
    Valhalla, New York 10595, United States
  • Duke Univ Med Ctr
    Durham, North Carolina 277103499, United States
  • Columbus Children's Hosp
    Columbus, Ohio 432052696, United States
  • Med Univ of South Carolina
    Charleston, South Carolina 294253312, United States
  • Saint Jude Children's Research Hosp of Memphis
    Memphis, Tennessee 381052794, United States
  • Children's Med Ctr of Dallas
    Dallas, Texas 75235, United States
  • San Juan City Hosp
    San Juan, 009367344, Puerto Rico
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 28, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00000750
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Glaxo Wellcome
Responsible party
Sponsor
First posted
Aug 31, 2001
Completion
Sep 1996
Last update
Oct 28, 2021

Study contacts

E Connor
study chair
G McSherry
study chair
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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