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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Follow-up Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies During Any Pregnancy Conceived Post Vaccination/Control

ClinicalTrials.gov ID: NCT05705440

Public ClinicalTrials.gov record NCT05705440. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 4:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b, Non-randomized, Open Label, Multi-country, Cohort Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies (RSV MAT-001, RSV MAT-004, RSV MAT-010, RSV MAT-011, RSV MAT-009, RSV MAT-012 and RSV MAT-039) During Any Pregnancy Conceived Post Vaccination/Control

Study identification

NCT ID
NCT05705440
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
3,855 participants

Conditions and interventions

Interventions

  • RSVPreF3 vaccine Biological
  • Control Other

Biological · Other

Eligibility (public fields only)

Age range
9 Years to 49 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 6, 2023
Primary completion
Jan 14, 2025
Completion
Jan 14, 2025
Last update posted
Mar 16, 2026

2023 – 2025

United States locations

U.S. sites
27
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
GSK Investigational Site Mobile Alabama 36608
GSK Investigational Site Phoenix Arizona 85015
GSK Investigational Site Tucson Arizona 85712
GSK Investigational Site Burbank California 91506
GSK Investigational Site Los Angeles California 90057
GSK Investigational Site Nampa Idaho 83686
GSK Investigational Site Nampa Idaho 83702
GSK Investigational Site Covington Louisiana 70433
GSK Investigational Site Slidell Louisiana 70458
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site Saginaw Michigan 48604
GSK Investigational Site Biloxi Mississippi 39531
GSK Investigational Site Albuquerque New Mexico 87107
GSK Investigational Site Englewood Ohio 45322
GSK Investigational Site Greenville South Carolina 29607
GSK Investigational Site Hendersonville Tennessee 29708
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site Houston Texas 77008
GSK Investigational Site Keller Texas 76012
GSK Investigational Site Keller Texas 76028
GSK Investigational Site Keller Texas 76051
GSK Investigational Site Lampasas Texas 76550
GSK Investigational Site Plano Texas 75093
GSK Investigational Site Weatherford Texas 76086
GSK Investigational Site Norfolk Virginia 68701
GSK Investigational Site Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 111 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05705440, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 16, 2026 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05705440 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →