A total of 96 subjects will be recruited into 5 groups. Each subject will receive either two vaccinations with MVA-BN-RSV vaccine or placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
MVA-mBN294B
Tris Buffered Saline
Occurrence of serious adverse events
Occurrence, relationship to the trial vaccine and intensity of any serious adverse event (SAE).
Time frame: Screening up to week 34 after first vaccination
RSV-specific humoral immune response
To assess the RSV-specific serum antibody responses
Time frame: humoral immune response is measured up to week 34
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