Last updated 35 days ago

Efficacy, Immunogenicity, and Safety Study of a Respiratory Syncytial Virus Vaccine in Infants and Toddlers

6300 patients around the world
Available in Honduras, Argentina, United States
Study duration will be 24 months for each participant. The safety follow-up will start at inclusion and up to the end of the study.
Sanofi Pasteur, a Sanofi Company
6300Patients around the world
This study is for people with
Respiratory syncytial virus
Requirements for the patient
To 21 Months
All Gender
Medical requirements
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