Respiratory Syncytial Virus Infections Clinical Trial
Official title:
A Randomized, Single-blind, Placebo Controlled, Dose-ranging Phase II Trial in ≥ 55 Year Old Adults to Evaluate the Safety and Immunogenicity of the Recombinant MVA-BN-RSV Vaccine
A total of 400 subjects will be recruited into five treatment subject groups à 80
subjects.Subject will receive two administrations 4 weeks apart which will consist of
MVA-BN-RSV Dose 1, MVA-BN-RSV Dose 2 or Placebo (TBS).
86 subjects from 2 treatment groups (43 per treatment group) are supposed to receive one
(booster) dose of MVA-BN-RSV vaccine approximately one year after their first vaccination. In
this booster substudy, eligible subjects will receive the same dose they received during the
main trial.
n/a
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