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Active, not recruiting Phase 3 Interventional Accepts healthy volunteers

Long-term Follow-up Study to Evaluate Safety and Immunogenicity of CHIKV VLP Single or Booster Vaccination

ClinicalTrials.gov ID: NCT06007183

Public ClinicalTrials.gov record NCT06007183. 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 Sep 6, 2026, 11:11 AM 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 Long-term Follow-up Study to Evaluate Safety and Immunogenicity of a Chikungunya Virus Virus-like Particle Vaccine (CHIKV VLP) in Healthy Adults and Adolescents After Either a Single or Booster Vaccination Dosing Regimen

Brief summary

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

The purpose of this phase 3 multicenter, randomized, double-blind, placebo-controlled rollover study is to evaluate the safety and long-term immunogenicity of CHIKV VLP vaccine in adult and adolescent participants and to evaluate CHIKV VLP booster vaccine induced serum neutralizing antibody (SNA) response at 3 or 4 years post-initial CHIKV VLP vaccination.

Study identification

NCT ID
NCT06007183
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bavarian Nordic
Industry
Enrollment
715 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
12 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
Aug 29, 2023
Primary completion
Jan 31, 2028
Completion
Jan 31, 2028
Last update posted
Aug 6, 2026

2023 – 2028

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Alliance for Multispecialty Research, LLC Mobile Alabama 36608
Alliance for Multispecialty Research, LLC Tempe Arizona 85281
Optimal Research, LLC Melbourne Florida 32934
Suncoast Research Associates, LLC Miami Florida 33173
Synexus Clinical Research US, Inc. Chicago Illinois 60602
Optimal Research, LLC Peoria Illinois 61614
Alliance for Multispecialty Research, LLC Newton Kansas 67114
Alliance for Multispecialty Research, LLC Wichita Kansas 67207
Alliance for Multispecialty Research, LLC Lexington Kentucky 40509
Alliance for Multispecialty Research, LLC Kansas City Missouri 64114
Wr-Crcn, Llc Las Vegas Nevada 89106
Alliance for Multispecialty Research, LLC Las Vegas Nevada 89119
Rochester Clinical Research, LLC Rochester New York 14609
M3 Wake Research Inc. Raleigh North Carolina 27612
Velocity Clinical Research, Cleveland Cleveland Ohio 44122
Lynn Institute of Norman Norman Oklahoma 73072
Velocity Clinical Research, Medford Medford Oregon 97504
Velocity Clinical Research, Providence East Greenwich Rhode Island 02818
Velocity Clinical Research, Austin Cedar Park Texas 78613
DM Clinical Research Houston Texas 77081
BFHC Research, LLC San Antonio Texas 78249
DM Clinical Research Tomball Texas 77375
Velocity Clinical Research, Salt Lake City West Jordan Utah 84088
Alliance for Multispecialty Research, LLC Norfolk Virginia 23502

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 NCT06007183, 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 Aug 6, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06007183 live on ClinicalTrials.gov.

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