A Study on the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine, in High Risk Pregnant Women Aged 15 to 49 Years and Infants Born to the Vaccinated Mothers

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE III, DOUBLE-BLIND, RANDOMIZED, PLACEBOCONTROLLED STUDY TO EVALUATE THE SAFETY, REACTOGENICITY AND IMMUNE RESPONSE OF A SINGLE INTRAMUSCULAR DOSE OF UNADJUVANTED RSV MATERNAL VACCINE, IN HIGH RISK PREGNANT WOMEN AGED 15 TO 49 YEARS AND INFANTS BORN TO THE VACCINATED MOTHERS.

Intervention/treatment:
RESPIRATORY SYNCYTIAL VIRUS (RSV) MATERNAL (RSVPREF3) VACCINE
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
214725 (RSV MAT-012)
Control number:
253128
Status:
Closed
Approved:
June 25, 2021
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04980391
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

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

Contacts and locations

Contact
Name
GSK Response Center
Organization
GlaxoSmithKline
Phone:
866-435-7343
Sponsor
GLAXOSMITHKLINE INC

Locations

Nova Scotia

GSK Investigational Site
Halifax, Nova Scotia, B3K 6R8

Quebec

GSK Investigational Site
Montreal, Quebec, H3T 1C5

Results

See the results from the trial NCT04980391. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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