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A Phase II Randomized, Observer-Blind, Placebo-Controlled Study to Evaluate the Immunogenicity and Safety of a Respiratory Syncytial Virus (RSV) Recombinant F Nanoparticle Vaccine in Healthy Older Adult Subjects Previously Treated With the Same Vaccine, or Placebo, in the Prior Year; and to Estimate the Incidence Rate of RSV Disease and Vaccine Efficacy in Subjects Based on Their RSV F Vaccine Experience Over Two Consecutive Years.
Conditions
Interventions
RSV-F Vaccine
Phosphate Buffer Placebo
Locations
10
United States
Nothern California Clinical Research
Redding, California, United States
Clinical Research Atlanta
Stockbridge, Georgia, United States
Johnson County Clin-Trials
Lenexa, Kansas, United States
Rapid Medical Research
Cleveland, Ohio, United States
Clinical Research Associates
Nashville, Tennessee, United States
Research Across America
Dallas, Texas, United States
Start Date
October 1, 2015
Primary Completion Date
November 1, 2016
Completion Date
November 1, 2016
Last Updated
May 27, 2022
NCT05045612
NCT06998251
NCT06521944
NCT07249320
NCT07128121
NCT04896853
Lead Sponsor
Novavax
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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