Prophylactic smallpox vaccination for personnel actively working with or in the vicinity of replicating vaccinia virus
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
22
IMVAMUNE® liquid -frozen, containing 1 x 10E8 TCID50 MVA-BN® per 0.5 mL dose
Palo Alto Medical Foundation
Palo Alto, California, United States
ELISA Seropositivity Rate
Seropositivity rate based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Seropositivity is defined as antibody titers ≥ detection limit (50). Percentages based on number of subjects with data available.
Time frame: up to Week 7
ELISA Seroconversion Rate
Seroconversion rate based on Enzyme-linked Immunosorbent Assay (ELISA). Seroconversion is defined as the appearance of antibody titers ≥ detection limit (50) for initially seronegative subjects, or a doubling or more of the antibody titer compared to the Screening titer for initially seropositive subjects. Percentages based on number of subjects with data available.
Time frame: Week 7
ELISA GMT
Geometric Mean Titers (GMT) based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Titers below the detection limit are included with a value of '1'.
Time frame: up to Week 7
Serious Adverse Events
Incidence, relationship and intensity of any Serious Adverse Event (SAE).
Time frame: up to 32 weeks
Related Grade >=3 Adverse Events
Incidence of any Grade \>=3 Adverse Events possibly, probably or definitely related to the trial vaccine
Time frame: within 29 days after any vaccination
Non-serious AEs
Incidence of non-serious AEs
Time frame: within 29 days after any vaccination
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