Respiratory Syncytial Virus (RSV) Vaccine

  • sponsor
Updated on 11 August 2021


This study will evaluate the efficacy of the RSVPreF3 OA investigational vaccine in preventing Lower Respiratory Tract Disease (LRTD) caused by RSV in adults ≥60 years of age in Northern Hemisphere (NH) and in Southern Hemisphere (SH). This study will also assess if the vaccine is safe and induces an immune response.


  • Condition: Vaccine
  • Drug: RSVPreF3 OA
  • Clinical Trial Identifier: NCT04886596
  • Sponsor: GlaxoSmithKline

Condition Vaccines
Clinical Study IdentifierTX279564
Last Modified on11 August 2021


Yes No Not Sure

Inclusion Criteria

Male or Female, 60 and older
Participants in overall good health

Exclusion Criteria

Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease (e.g. current malignancy, human immunodeficiency virus) or immunosuppressive/cytotoxic therapy (e.g., medication used during cancer chemotherapy, organ transplantation, or to treat autoimmune disorders), based on medical history and physical examination (no laboratory testing required)
Previous vaccination with an RSV vaccine
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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