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Antibody Persistence And Long Term Safety Of A Chikungunya Virus Vaccine (VLA1553)
NCT04838444 · View on ClinicalTrials.gov ↗
Study Summary
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).
Conditions Studied
Interventions
- BIOLOGICAL VLA1553
Study Locations (10)
Nebraska
- Velocity Clinical Research — Grand Island
- Velocity Clinical Research — Omaha
Arizona
- Accelerated Enrollment Solutions (AES) — Phoenix
Florida
- Velocity Clinical Research — Hallandale
Illinois
- Accelerated Enrollment Solutions (AES) — Chicago
Kentucky
- Alliance for Multispecialty Research (AMR) — Lexington
Tennessee
- Alliance for Multispecialty Research (AMR) — Knoxville
Texas
- Velocity Clinical Research — Austin
Utah
- Velocity Clinical Research — West Jordan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 363 participants |
| Start Date | 2021-04-02 |
| Est. Completion | 2031-05 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04838444
The ClinicalTrials.gov registry entry for NCT04838444 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 363 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Valneva Austria, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chikungunya Virus Infection appearing as the primary indexed condition, and to 1 intervention — of which VLA1553 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04838444 reports 10 study locations spanning 9 distinct geographic areas — top geographies include Nebraska, Arizona, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04838444 about?
NCT04838444 is a clinical study titled "Antibody Persistence And Long Term Safety Of A Chikungunya Virus Vaccine (VLA1553)". 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).
What is the current status of trial NCT04838444?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 363 participants. The study started on 2021-04-02. Estimated completion is 2031-05.
What conditions does trial NCT04838444 study?
This clinical trial studies the following conditions: Chikungunya Virus Infection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04838444?
The interventions under investigation include: VLA1553 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04838444?
This trial is sponsored by Valneva Austria, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04838444 being conducted?
This trial has 10 study locations across Arizona, Florida, Illinois, Kentucky, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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