A Study of 3 Lots of an Investigational Vaccine Against Respiratory Syncytial Virus (RSV) in Adults Aged 60 Years and Above

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Updated on 5 March 2022
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The purpose of this study is to assess the lot-to-lot consistency in terms of immunogenicity and evaluate the safety and reactogenicity of 3 lots of the RSVPreF3 OA investigational vaccine administered as a single dose in adults ≥ 60 years of age (YOA).

Condition Respiratory Syncytial Virus Infections
Treatment RSVPreF3 OA investigational vaccine
Clinical Study IdentifierNCT05059301
Last Modified on5 March 2022

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