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Last updated 35 days ago
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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
6300
Patients around the world
This study is for people with
Respiratory syncytial virus
Requirements for the patient
To 21 Months
All Gender
Medical requirements
Inclusion criteria
Exclusion criteria
See details
Contact us
Contact us
Study
PEARL
Sponsor
Sanofi Pasteur, a Sanofi Company
Conditions
Requirements
To 21 Months
All Gender
Unique study ID
clinicaltrials.gov
NCT06252285
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