HIV Infections Clinical Trial
Official title:
A Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of 200 Mcg of gp120 (CHO) BIOCINE in MF59 Emulsion Versus the Emulsion Control: Three Injections at 0, 1, and 6 Months
To evaluate in healthy volunteers the safety and immune response to 200 mcg gp120 candidate
vaccine in MF59 emulsion without MTP-PE at 0, 1 and 6 months.
Preliminary evaluations of two dose levels of gp120 administered to volunteers in protocol
VEU 007A indicate that a gp120 dose of potentially greater immunogenicity may be of
interest.
Preliminary evaluations of two dose levels of gp120 administered to volunteers in protocol
VEU 007A indicate that a gp120 dose of potentially greater immunogenicity may be of
interest.
Ten healthy volunteers receive 200 mcg gp120 in MF59 emulsion, and four volunteers receive
placebo consisting of MF59 emulsion in PBS vehicle. Injections are given at months 0, 1, and
6. Patients are followed for 12 months following the third injection.
;
Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Primary Purpose: Prevention
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