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NCT03992872 · ClinicalTrials.gov registry record · Phase 2

Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317)

A Phase 2 study of Chikungunya, sponsored by Bavarian Nordic.

Completed
Registry status
Phase 2
Development phase
60
Enrollment target
2
Study locations

NCT03992872 is a Phase 2 study of Chikungunya that has completed, run by Bavarian Nordic. The registered enrollment target is 60 participants. The trial reports 2 study locations across 1 state.

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The verdict

NCT03992872, a Phase 2 study of Chikungunya, has completed, sponsored by Bavarian Nordic.

COMPLETED
Registry status
Phase 2
Development phase
60 participants
Enrollment target
2
Study locations

Study Summary

This was a phase 2 parallel-group age- and gender-matched open label study in healthy adults 18-65 years of age to assess the safety and immunogenicity of an alum-adjuvanted chikungunya virus-like particle vaccine (PXVX0317; CHIKV VLP vaccine) in prior recipients of other alphavirus vaccines versus alphavirus naïve controls.

Conditions Studied

Interventions

  • BIOLOGICAL Chikungunya

Study Locations (2)

Maryland

  • United States Army Medical Research Institute of Infectious Diseases - Fort Deterick
  • Walter Reed Army Institute of Research - Silver Spring

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2019-11-20
Est. Completion 2021-01-19
Phase Phase 2

Sponsor

Bavarian Nordic

41 total trials

What the Registry Record Tells You About NCT03992872

The ClinicalTrials.gov registry entry for NCT03992872 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bavarian Nordic, which has 41 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chikungunya appearing as the primary indexed condition, and to 1 intervention - of which Chikungunya is the first listed.

NCT03992872 reports 2 study locations spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT03992872 about?

NCT03992872 is a clinical study titled "Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317)". This was a phase 2 parallel-group age- and gender-matched open label study in healthy adults 18-65 years of age to assess the safety and immunogenicity of an alum-adjuvanted chikungunya virus-like particle vaccine (PXVX0317; CHIKV VLP vaccine) in prior recipients of other alphavirus vaccines versus ...

What is the current status of trial NCT03992872?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2019-11-20. Estimated completion is 2021-01-19.

What conditions does trial NCT03992872 study?

This clinical trial studies the following conditions: Chikungunya.

What interventions are being tested in trial NCT03992872?

The interventions under investigation include: Chikungunya (BIOLOGICAL).

Who is sponsoring clinical trial NCT03992872?

This trial is sponsored by Bavarian Nordic, which has 41 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03992872 being conducted?

This trial has 2 study locations across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.