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Sponsored by: |
National Institute of Allergy and Infectious Diseases (NIAID) |
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Information provided by: | National Institute of Allergy and Infectious Diseases (NIAID) |
ClinicalTrials.gov Identifier: | NCT00000809 |
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.
Condition | Intervention | Phase |
---|---|---|
HIV Infections HIV Seronegativity |
Biological: Aluminum hydroxide Biological: QS-21 Biological: MN rsgp120/HIV-1 |
Phase I |
Study Type: | Interventional |
Study Design: | Prevention, Dose Comparison |
Official Title: | A Phase I Trial of the Safety and Immunogenicity of MN rsgp120/HIV-1 With the Adjuvants QS-21 and Alum Compared to MN rsgp120/HIV-1 and QS-21 in Infants Born to HIV-Infected Women |
Ages Eligible for Study: | up to 3 Days |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria
Infants may be eligible for this study if they:
Study ID Numbers: | ACTG 279 |
Study First Received: | November 2, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000809 |
Health Authority: | United States: Federal Government |
HIV Preventive Vaccine HIV Therapeutic Vaccine |
Virus Diseases Sexually Transmitted Diseases, Viral Aluminum sulfate HIV Infections Sexually Transmitted Diseases |
Acquired Immunodeficiency Syndrome QS 21 Retroviridae Infections Immunologic Deficiency Syndromes Aluminum Hydroxide |
RNA Virus Infections Slow Virus Diseases Immunologic Factors Molecular Mechanisms of Pharmacological Action Immune System Diseases Physiological Effects of Drugs |
Adjuvants, Immunologic Lentivirus Infections Antacids Infection Pharmacologic Actions |