The purpose of this study is to assess the safety and immunogenicity of two MVA smallpox vaccine injections in healthy adults that are 18-35 years of age with HIV infection
This is a multi-center study 90 HIV-seropositive subjects. There will be an injection of MVA smallpox vaccine or placebo on day 0 and day 28. Subjects will be enrolled and vaccinated in two cohorts according to CD4 cell count levels and number of subjects vaccinated. Excluding the screening period, the study duration will be approximately 56 days with a follow up safety visit at study day 148 and a telephone health status interview at study day 208.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
2
0.5mL of MVA3000 Smallpox Vaccine, 2 doses, separated by 28 days.
University of Alabama at Birmingham
Birmingham, Alabama, United States
AltaMed Health Services Corporation
Los Angeles, California, United States
Quest Clinical Research
San Francisco, California, United States
University of Miami AIDS Clinical Research Unit
Miami, Florida, United States
Safety
Time frame: Study Completion
Immunogenicity
Time frame: Study Completion
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University of Miami School of Medicine
Miami, Florida, United States
University of Hawaii
Honolulu, Hawaii, United States