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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Phase 3 Lot to Lot Consistency Study of Live Oral Cholera Vaccine, PXVX0200 in Healthy Adults

ClinicalTrials.gov ID: NCT02094586

Public ClinicalTrials.gov record NCT02094586. 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 Apr 29, 2026, 6:22 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

Phase 3 Randomized, Double-blind, Placebo-Controlled 3-Lot Study in Healthy Volunteers to Assess Immunogenicity, & Acceptability of a Single-dose of Live Oral Cholera Vaccine, Vibrio Cholerae O1 Serotype Inaba Vaccine Strain CVD 103-HgR

Study identification

NCT ID
NCT02094586
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bavarian Nordic
Industry
Enrollment
3,146 participants

Conditions and interventions

Conditions

Interventions

  • PXVX0200 Lot A Biological
  • PXVX0200 Lot B Biological
  • PXVX0200 Lot C Biological
  • Placebo Biological

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
Apr 30, 2014
Primary completion
Jan 31, 2015
Completion
May 31, 2015
Last update posted
Jun 27, 2023

2014 – 2015

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Coastal Clinical Research Mobile Alabama 36608
Clinical Reseach Consortium Arizona Phoenix Arizona 85004
Avail Clinical Research DeLand Florida 32720
Miami Research Associates Miami Florida 33143
Palm Beach Research West Palm Beach Florida 33409
Emory University Atlanta Georgia 30322
Johnson County Clin-Trials Lenexa Kansas 66219
Heartland Research Associates Wichita Kansas 67207
Central Kentucky Research Lexington Kentucky 40509
University of Kentucky Lexington Kentucky 40536
Boston University Boston Massachusetts 02218
Center for Pharmaceutical Research Kansas City Missouri 64114
St. Louis University St Louis Missouri 63104
Clinical Research Consortium Las Vegas Las Vegas Nevada 89119
Rochester Clinical Research Rochester New York 14609
Lion Research Norman Oklahoma 73069
Coastal Carolina Research Mt. Pleasant South Carolina 29464
Research Across America Dallas Texas 75234
Jean Brown Research Salt Lake City Utah 84124

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02094586, 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 Jun 27, 2023 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02094586 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →