Safety and Effectiveness of Two Different Formulations of an HIV Vaccine in Infants Born to HIV-Infected Women
NCT00000809 · Status: WITHDRAWN · Phase: PHASE1 · Type: INTERVENTIONAL
Last updated 2021-10-29
Summary
The purpose of this study is to test the safety and effectiveness of two different formulations of an HIV vaccine in infants born to HIV-infected women.
Conditions
- HIV Infections
- HIV Seronegativity
Interventions
- BIOLOGICAL
-
Aluminum hydroxide
- BIOLOGICAL
-
QS-21
- BIOLOGICAL
-
MN rsgp120/HIV-1
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Study Design
- Purpose
- PREVENTION
Eligibility
- Min Age
- 1 Day
- Max Age
- 3 Days
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
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