Status and phase
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About
Comparative assessment of the tolerability, safety, and immunogenicity of the Flu-M® Inactivated Split Influenza Vaccine (without preservative) and the Flu-M® vaccine (with preservative) in volunteers aged between 18 and 60
Full description
Single administration of the trial products. Duration of follow-up - 28+3 (outpatient visit) and Long-term follow-up - 180±3 days.
Enrollment
Sex
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Volunteers
Inclusion criteria
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Primary purpose
Allocation
Interventional model
Masking
654 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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