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A Randomized, Double-blind, Placebo-controlled Phase 3 Study to Evaluate Efficacy, Safety, Reactogenicity, and Immunogenicity of an Ad26.RSV.preF-based Vaccine in Japanese Adults Aged 60 Years and Older, and Safety, Reactogenicity, and Immunogenicity of the Vaccine in Japanese Adults Aged 20 to 59 Years at High-risk of RSV Disease
Conditions
Interventions
Ad26/protein preF RSV Vaccine
Placebo
Locations
30
Japan
Shohokai Toda Internal Medicine and Neurology Clinic
Akashi-shi, Japan
Doujin Memorial Meiwa Hospital
Chiyoda-ku, Japan
Fukuwa Clinic
Chūō, Japan
Tokyo-Eki Center-Building Clinic
Chūōku, Japan
Tokyo Asbo Clinic
Chūōku, Japan
Tenjin Sogo Clinic
Fukuoka, Japan
Start Date
April 1, 2022
Primary Completion Date
March 20, 2023
Completion Date
March 20, 2023
Last Updated
May 23, 2025
NCT07177508
NCT05083585
Lead Sponsor
Janssen Pharmaceutical K.K.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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