A Phase III Study to Assess the Lot-to-lot Consistency of GSK's Investigational RSV Maternal Vaccine and the Immune Response and Safety of RSV Maternal Vaccine When Given Alone or Co-administered With GSK's Influenza D-QIV Vaccine in Healthy Non-pregna…

Last updated:
2026-07-11
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol title:

A PHASE III, OBSERVER-BLIND, RANDOMIZED, MULTICOUNTRY STUDY TO EVALUATE THE LOT-TO-LOT CONSISTENCY OF GSK¿S INVESTIGATIONAL RSV MATERNAL VACCINE AND THE IMMUNE RESPONSE, SAFETY AND REACTOGENICITY OF RSV MATERNAL VACCINE WHEN CO-ADMINISTERED WITH GSK¿S QUADRIVALENT INFLUENZA D-QIV VACCINE IN HEALTHY NON-PREGNANT WOMEN 18-49 YEARS OF AGE

Intervention/treatment:
RESPIRATORY SYNCYTIAL VIRUS (RSV) MATERNAL (RSVPREF3) VACCINE
Medical condition:
RESPIRATORY SYNCYTIAL VIRUS
Protocol code:
214709 (RSV MAT-010)
Control number:
254764
Status:
Closed
Approved:
August 13, 2021
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT05045144
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: FEMALE
Age
18 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

British Columbia

GSK Investigational Site
Surrey, British Columbia, V3S 2N6
GSK Investigational Site
Vancouver, British Columbia, V6Z 2T1

Nova Scotia

GSK Investigational Site
Truro, Nova Scotia, B2N 1L2

Ontario

GSK Investigational Site
London, Ontario, N5W 6A2
GSK Investigational Site
Sarnia, Ontario, N7T 4X3
GSK Investigational Site
Toronto, Ontario, M9W 4L6

Quebec

GSK Investigational Site
Mirabel, Quebec, J7J 2K8
GSK Investigational Site
Pointe-Claire, Quebec, H9R 4S3
GSK Investigational Site
Québec, Quebec, G1W 4R4
GSK Investigational Site
Saint-Charles-Borromée, Quebec, J6E 2B4
GSK Investigational Site
Sherbrooke, Quebec, J1L 0H8

Results

See the results from the trial NCT05045144. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?