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To determine the safety and immunogenicity of rgp120/HIV-1SF2 combined with MF59 adjuvant emulsion versus MF59 alone in HIV-negative volunteers. One approach to improve the immunogenicity of an HIV-1 subunit protein vaccine is to combine the immunogen with an adjuvant.
One approach to improve the immunogenicity of an HIV-1 subunit protein vaccine is to combine the immunogen with an adjuvant. Healthy volunteers receive intramuscular injections of rgp120/HIV-1SF2 with MF59 adjuvant emulsion or MF59 alone at months 0, 1, 6, 9, 10 and 12 (was months 0, 1, 6 and 10, amended 12/19/96).
Age
18 - 60 years
Sex
ALL
Healthy Volunteers
Yes
UAB AVEG
Birmingham, Alabama, United States
St. Louis Univ. School of Medicine AVEG
St Louis, Missouri, United States
Univ. of Rochester AVEG
Rochester, New York, United States
JHU AVEG
Pittsburgh, Pennsylvania, United States
Completion Date
January 1, 1998
Last Updated
November 4, 2021
30
ACTUAL participants
MF59
BIOLOGICAL
rgp120/HIV-1 SF-2
BIOLOGICAL
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NCT04142047
NCT06694805
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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