Influenza Clinical Trial
Official title:
Prospective, Multicenter, Double-blind, Randomized, Comparative Immunogenicity and Safety Trial of Flu-M [Inactivated Split Influenza Vaccine], Solution for Intramuscular Injection, 0.5 ml (FSUE SPbSRIVS FMBA), vs. Ultrix®, Solution for Intramuscular Injection, 0.5 ml (FORT LLC) in Volunteers Aged Over 60 Years
This trial by its design was a prospective, multicenter, double blind, randomized comparative clinical trial of the IIIb-IV phase which was carried out in parallel groups of volunteers over the age of 60
The volunteers will include in the trial will divide into two groups: Group 1: volunteers who will receive one dose of Flu-M, solution for intramuscular injection, 0.5 mL, intramuscularly. Group 2: volunteers who will receive one dose of Ultrix®, solution for intramuscular administration, 0.5 mL, intramuscularly. The trial include the following periods and visits: 1. Screening period (up to 7 days): • Visit 0 (day -7...-1). 2. Vaccination period (up to 1 day): • Visit 1 (day 1, randomization, blood collection for serological examination, vaccination). 3. Follow-up period (up to 28(+2) days): - Visit 2 (day 3, organization of trials to assess safety); - Visit 3 (day 7(+1), organization of trials to assess safety); - Visit 4 (day 21(+2), organization of trials to assess safety, blood collection for serological study); - Visit 5 (day 28(+2), organization of trials to assess safety, trial completion); ;
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