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A PHASE 3, RANDOMIZED, DOUBLE- OR OBSERVER-BLINDED, PLACEBO-CONTROLLED TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF A RESPIRATORY SYNCYTIAL VIRUS (RSV) PREFUSION F SUBUNIT VACCINE IN INFANTS BORN TO WOMEN VACCINATED DURING PREGNANCY

Study

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Details
Age

Child to Adult

Type of Study

Treatment

Locations

Childrens Hospital Colorado
Outpatient CTRC
University of Colorado Hospital

Principal Investigator
Eric Simoes,  MD

Eric Simoes, MD

Study ID

Protocol Number: 20-0481

More information available at ClinicalTrials.gov: NCT04032093

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