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A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF 3 LOTS OF RESPIRATORY SYNCYTIAL VIRUS (RSV) PREFUSION F SUBUNIT VACCINE IN HEALTHY ADULTS

NCT05096208 is registered in ClinicalTrials.gov with Pfizer as lead sponsor.

NCT NCT05096208
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Registry record

As filed in ClinicalTrials.gov.

Title
A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF 3 LOTS OF RESPIRATORY SYNCYTIAL VIRUS (RSV) PREFUSION F SUBUNIT VACCINE IN HEALTHY ADULTS
Lead sponsor
Pfizer
Phase
Phase 3
Overall status
Completed
Start date
October 21, 2021
Completion date
April 4, 2022
Enrollment
1,028 (actual)
Sites
18

Conditions

As the registry lists them; a condition with its own page is linked.

rsv