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Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317)

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Contents

clinicaltrials.gov/study/NCT03992872
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT039928720
Health Conditions in Trial
Chikungunya
Chikungunya
0
Trial Recruitment Size
600
Trial Sponsor
Bavarian Nordic
Bavarian Nordic
0
Trial Collaborator
Emergent BioSolutions
Emergent BioSolutions
0
Clinical Trial Start Date
November 20, 2019
0
Primary Completion Date
January 19, 2021
0
Study Completion Date
January 19, 2021
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Prevention0
Intervention Type
Biological0
Intervention Name
Chikungunya0
Interventional Trial Phase
Phase 20
Participating Facility
Walter Reed Army Institute of Research
Walter Reed Army Institute of Research
0
United States Army Medical Research Institute of Infectious Diseases
United States Army Medical Research Institute of Infectious Diseases
0
Official Name
A Phase 2 Open-label Study to Assess the Safety and Immunogenicity of an Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317) in Prior Recipients of Other Alphavirus Vaccines Versus Alphavirus Naïve Controls0
Last Updated
July 3, 2023
0
Allocation Type
Non-Randomized0
Intervention Model
Parallel Assignment0
Masking Type
None (Open Label)0
Study summary

This is a Phase 2 parallel-group age- and gender-matched open label study in healthy adults 18-65 years of age to assess the safety and immunogenicity of an alum-adjuvanted chikungunya virus-like particle vaccine (PXVX0317) in prior recipients of other alphavirus vaccines versus alphavirus naïve controls.

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