A Trial to Evaluate the Efficacy and Safety of RSVpreF in Infants Born to Women Vaccinated During Pregnancy.

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 3, RANDOMIZED, DOUBLE-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

Intervention/treatment:
PF-06928316 (RESPIRATORY SYNCYTIAL VIRUS [RSVPREF] VACCINE)
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
C3671008
Control number:
238437
Status:
Closed
Approved:
May 15, 2020
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04424316
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: FEMALE
Age
0 Years to 49 Years
Accepts healthy volunteers: Yes

Contacts and locations

Contact
Name
PfizerClinicalTrials.gov Call Center
Organization
Pfizer Inc.
Phone:
1-800-718-1021
Sponsor
PFIZER CANADA ULC

Locations

Nova Scotia

Canadian Center for Vaccinology - IWK Health Centre
Halifax, Nova Scotia, B3K 6R8

Quebec

CHU de Québec-Université Laval
Québec, Quebec, G1V 4G2
CHU Sainte-Justine
Montreal, Quebec, H3T 1C5

Results

See the results from the trial NCT04424316. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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