Respiratory Syncytial Virus (RSV)

  • sponsor
    Janssen Vaccines & Prevention B.V.
Updated on 14 January 2022


The study will enroll up to 23000 participants in order to demonstrate the efficacy of the active Ad26.RSV.preF-based study vaccine in the prevention of Reverse Transcription Polymerase Chain Reaction (RT-PCR) confirmed Respiratory Syncytial Virus (RSV)-mediated Lower Respiratory Tract Disease (LRTD) when compared to placebo in adults aged 60 years and above.


  • Condition: Respiratory Syncytial Virus (RSV)
  • Clinical Trial Identifier: NCT04908683
  • Sponsor: Janssen Vaccines & Prevention B.V.

Condition Vaccines
Clinical Study IdentifierTX290678
SponsorJanssen Vaccines & Prevention B.V.
Last Modified on14 January 2022


Yes No Not Sure

Inclusion Criteria

Age 60+
Must be able to work with smartphones/tablets/computers
From the time of vaccination through 3 months after vaccination, participant agrees not to donate blood
Must be willing to provide verifiable identification, has means to be contacted and to contact the investigator during the study

Exclusion Criteria

Has a serious clinically unstable condition, (example, end-stage renal disease with or without dialysis, clinically unstable cardiac disease), Alzheimer's disease, or any other condition for which, in the opinion of the investigator, participation would not be in the best interest of the participant (example, compromise well-being) or that could prevent, confound, or limit the protocol specified assessments
History of malignancy within 5 years before screening or revaccination not in the following categories: a. Participants with squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix may be enrolled at the discretion of the investigator; b. Participants with a history of malignancy within 5 years, which is considered cured with minimal risk of recurrence per investigator's judgement, can be enrolled
Had major surgery (example, major cardiopulmonary or abdominal operations) as per the investigator's judgment within 4 weeks before vaccination, or will not have fully recovered from surgery, or has major surgery planned during the time the participant is expected to participate in the study
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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.
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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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