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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study to Demonstrate Consistency of Three Lots of a Live-attenuated Chikungunya Virus Vaccine Candidate in Healthy Adults

ClinicalTrials.gov ID: NCT04786444

Public ClinicalTrials.gov record NCT04786444. 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 19, 2026, 7:10 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 Randomized, Double-Blinded Phase 3 Study to Demonstrate Lot-to-Lot Consistency of Three Lots of a Live-Attenuated Chikungunya Virus Vaccine Candidate (VLA1553) in Healthy Adults Aged 18 to 45 Years

Brief summary

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

This was a prospective, randomized, double-blinded, multicenter Phase 3 clinical study investigating three Lots of VLA1553 at the final dose. Overall 409 healthy subjects aged 18 to 45 years were randomized into the study.

Study identification

NCT ID
NCT04786444
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Valneva Austria GmbH
Industry
Enrollment
409 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 45 Years
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
Feb 22, 2021 (Actual)
Primary completion
Jul 22, 2021 (Actual)
Completion
Jan 26, 2022 (Actual)
Last update posted
Sep 28, 2023

2021 – 2022

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
AMR Miami Coral Gables Florida 33134 —
AMR Fort Myers Fort Myers Florida 33912 —
St. Johns Center for Clinical Research Ponte Vedra Florida 32081 —
AMR Wichita West Wichita Kansas 67205 —
AMR Lexington Lexington Kentucky 40509 —
Walter Reed Amy Institute of Research Silver Spring Maryland 20910 —
Alliance for Multispecialty Research (AMR) Kansas City Missouri 64114 —
Meridian Clinical Research Omaha Nebraska 68134 —
Wr-Crcn, Llc Las Vegas Nevada 89104 —
Rochester Clinical Research Rochester New York 14609 —
AMR Knoxville Knoxville Tennessee 37919 —
Dynamed Clinical Research Tomball Texas 77375 —

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 NCT04786444, 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 Sep 28, 2023 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04786444 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →