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Vaccine Effectiveness of a Bivalent RSV Prefusion F Protein-Based Vaccine for Preventing RSV Hospitalizations in Adults
Vaccine Effectiveness of a Bivalent RSV Prefusion F Protein-Based Vaccine for Preventing RSV Hospitalizations in Adults

NCT06684743

Active Not RecruitingPhase 4

Sponsor: Tor Biering-Sørensen

Conditions: RSV

Interventions: RSV prefusion F protein-based vaccine

Countries: Denmark, Spain

The purpose of this pragmatic randomized trial is to evaluate the vaccine effectiveness of bivalent RSV prefusion F vaccine (RSV vaccine) in adults. Participants will be randomized 1:1 to either RSV vaccine or no RSV vaccine.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: Yes

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria

* Age 18 years and above
* Informed consent form has been signed and dated

Exclusion Criteria:

* There are no specific exclusion criteria for this study
Locations (3)
  • Copenhagen, Denmark
  • Søborg, Denmark
  • Santiago de Compostela, A Coruña, Spain