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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years

ClinicalTrials.gov ID: NCT05349617

Public ClinicalTrials.gov record NCT05349617. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Safety and Immunogenicity Trial of the VLP-Based Chikungunya Virus Vaccine PXVX0317 in Adults ≥65 Years of Age

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this phase 3, randomized, double-blind, placebo-controlled study is to evaluate the safety and immunogenicity to PXVX0317 in adults ≥65 years of age.

Study identification

NCT ID
NCT05349617
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bavarian Nordic
Industry
Enrollment
413 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
65 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 12, 2022 (Actual)
Primary completion
Jun 19, 2023 (Actual)
Completion
Aug 8, 2023 (Actual)
Last update posted
Dec 13, 2024

2022 – 2023

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Suncoast Research Associates, LLC Miami Florida 33173 —
Panax Clinical Research Miami Lakes Florida 33014 —
Global Clinical Research Professionals (GCP) St. Petersburg Florida 33705 —
AMR Kansas City Kansas City Missouri 64114 —
Rochester Clinical Research, Inc. Rochester New York 14609 —
Coastal Carolina Research Center North Charleston South Carolina 29405 —
DM Clinical Research CyFair Houston Texas 77065 —
BHFC Research San Antonio Texas 78249 —
DM Clinical Research Tomball Tomball Texas 77375 —
Spaulding Clinical West Bend Wisconsin 53095 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05349617, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 13, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05349617 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →