A Study on the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine, in High Risk Pregnant Women Aged 15 to 49 Years and Infants Born to the Vaccinated Mothers

    Not Recruiting
  • End date
    Jul 10, 2023
  • participants needed
  • sponsor
Updated on 23 May 2022
Accepts healthy volunteers


The purpose of this study is to evaluate the safety, reactogenicity and immune response of a single intramuscular dose of the respiratory syncytial virus (RSV) maternal vaccine compared to placebo, when administered in the second or third trimester of pregnancy in women, 15 to 49 years of age (YOA), with high risk pregnancies and in the infants born to the vaccinated mothers.

Condition Respiratory Syncytial Virus Infections
Treatment Placebo, RSV MAT
Clinical Study IdentifierNCT04980391
Last Modified on23 May 2022

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