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A Phase III, Randomized, Multi-country 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

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Trial Profile

A Phase III, Randomized, Multi-country 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

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 17 Jul 2024

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At a glance

  • Drugs GSK 2321138A (Primary) ; GSK-3888550A (Primary)
  • Indications Respiratory syncytial virus infections
  • Focus Adverse reactions; Pharmacodynamics; Registrational
  • Acronyms RSV MAT-010
  • Sponsors GlaxoSmithKline; GlaxoSmithKline Biologicals; GSK

    • Most Recent Events

    • 22 Aug 2022 The trial has been completed in Finland(Date of the global end of the trial: 6 Jun 2022), according to European Clinical Trials Database record.
    • 23 Dec 2021 Planned End Date changed from 29 May 2022 to 16 Jun 2022.
    • 23 Dec 2021 Planned primary completion date changed from 23 Dec 2021 to 10 Jan 2022.

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