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Active, not recruiting Phase 3 Interventional Accepts healthy volunteers Results available

Antibody Persistence And Long Term Safety Of A Chikungunya Virus Vaccine (VLA1553)

ClinicalTrials.gov ID: NCT04838444

Public ClinicalTrials.gov record NCT04838444. 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 2, 2026, 3:52 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

An Open-Label, Single Arm Trial To Evaluate Antibody Persistence And Long Term Safety Of A Live-Attenuated Chikungunya Virus Vaccine (VLA1553) In Adults Aged 18 Years and Above

Brief summary

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

In this open-label Phase 3b, single arm trial, persistence of antibodies and long term safety will be evaluated in up to 375 participants rolled over from trial VLA1553-301 (NCT number: NCT04546724).

Study identification

NCT ID
NCT04838444
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Valneva Austria GmbH
Industry
Enrollment
363 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 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
Apr 1, 2021
Primary completion
Mar 2, 2023
Completion
Apr 30, 2031
Last update posted
Jul 8, 2026

2021 – 2031

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Accelerated Enrollment Solutions (AES) Phoenix Arizona 85020
Velocity Clinical Research Hallandale Florida 33090
Accelerated Enrollment Solutions (AES) Chicago Illinois 60602
Alliance for Multispecialty Research (AMR) Lexington Kentucky 40509
Velocity Clinical Research Grand Island Nebraska 68803
Velocity Clinical Research Omaha Nebraska 68134
Alliance for Multispecialty Research (AMR) Knoxville Tennessee 37920
Velocity Clinical Research Austin Texas 78759
Velocity Clinical Research West Jordan Utah 84088
Allliance for Multispecialty Research (AMR) 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 NCT04838444, 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 Jul 8, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04838444 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →