Actively Recruiting
Vaccine Effectiveness of a Bivalent RSV Prefusion F Protein-Based Vaccine for Preventing RSV Hospitalizations in Adults
Led by Tor Biering-Sørensen · Updated on 2025-11-25
690000
Participants Needed
3
Research Sites
193 weeks
Total Duration
On this page
Sponsors
T
Tor Biering-Sørensen
Lead Sponsor
P
Pfizer
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Vaccine Effectiveness of a Bivalent RSV Prefusion F Protein-Based Vaccine for Preventing RSV Hospitalizations in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years and above
- Informed consent form has been signed and dated
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Center for Translational Cardiology and Pragmatic Randomized Trials Department of Cardiology Copenhagen University Hospital - Herlev and Gentofte
Copenhagen, Denmark, 2900
Not Yet Recruiting
2
Danske Lægers Vaccinations Service
Søborg, Denmark, 2860
Actively Recruiting
3
General Public Health Directorate of Galician Health Service
Santiago de Compostela, A Coruña, Spain
Actively Recruiting
Research Team
M
Mats H Lassen, MD
CONTACT
T
Tor Biering-Sørensen, MD, PhD, MSc, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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