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ACTIVE NOT RECRUITING Phase 2

A Phase 2 Trial in Healthy Adult Participants of the Recombinant MVA-BN-WEV Vaccine

NCT06899802 · View on ClinicalTrials.gov ↗

Study Summary

This phase 2 clinical trial will investigate an optimal dose, dosing regimen, and evaluate reactogenicity, safety and immunogenicity in healthy adult participants of the recombinant, multivalent MVA-BN-WEV vaccine. MVA-BN-WEV is intended for active immunization for prevention of disease induced by VEEV and EEEV, in persons aged 18 years and older at high risk of exposure.

Conditions Studied

Interventions

  • OTHER Placebo
  • BIOLOGICAL MVA-BN-WEV

Study Locations (9)

Missouri

  • Jefferson City Medical Group / Avacare — Jefferson City
  • Clay-Platte Family Medicine, P.C./CCT Research — Kansas City

California

  • Benchmark Research — Sacramento

Georgia

  • Lifeline Primary Care, Inc. / CCT Research — Lilburn

Kansas

  • Johnson County Clin-Trials — Lenexa

Kentucky

  • Versailles Family Medicine, PLLC/CCT Research — Versailles

Louisiana

  • Benchmark Research — Kenner

Nebraska

  • Papillion Research Center/CCT Research — Papillion

Texas

  • Benchmark Research — San Angelo

Trial Details

FieldValue
Enrollment Target 411 participants
Start Date 2025-03-10
Est. Completion 2027-03
Phase Phase 2

Sponsor

Bavarian Nordic

16 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06899802

The ClinicalTrials.gov registry entry for NCT06899802 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 411 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bavarian Nordic, which has 16 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 Encephalitis appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT06899802 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Missouri, California, Georgia. 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 NCT06899802 about?

NCT06899802 is a clinical study titled "A Phase 2 Trial in Healthy Adult Participants of the Recombinant MVA-BN-WEV Vaccine". This phase 2 clinical trial will investigate an optimal dose, dosing regimen, and evaluate reactogenicity, safety and immunogenicity in healthy adult participants of the recombinant, multivalent MVA-BN-WEV vaccine. MVA-BN-WEV is intended for active immunization for prevention of disease induced by V...

What is the current status of trial NCT06899802?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 411 participants. The study started on 2025-03-10. Estimated completion is 2027-03.

What conditions does trial NCT06899802 study?

This clinical trial studies the following conditions: Encephalitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06899802?

The interventions under investigation include: Placebo (OTHER), MVA-BN-WEV (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06899802?

This trial is sponsored by Bavarian Nordic, which has 16 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06899802 being conducted?

This trial has 9 study locations across California, Georgia, Kansas, Kentucky, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial