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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Inactivated Split Virus Seasonal Influenza Vaccine (Vero Cell-Derived)

ClinicalTrials.gov ID: NCT01773928

Public ClinicalTrials.gov record NCT01773928. 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 Jul 23, 2026, 3:54 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

Randomized, Age-stratified, Double Blind, Controlled Phase 3 Study Comparing a Vero Cell-derived Trivalent Seasonal Influenza Vaccine Made by the Modified Manufacturing Process With Vaccine Made by the Current Manufacturing Process and a Licensed Trivalent Influenza Vaccine in Healthy Adults Aged 18 Years and Older

Study identification

NCT ID
NCT01773928
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Alachua Government Services, Inc.
Industry
Enrollment
1,928 participants

Conditions and interventions

Conditions

Interventions

  • Vero cell-derived trivalent influenza vaccine manufactured with the modified manufacturing process (VCIV modified) Biological
  • VCIV manufactured with the current manufacturing process (VCIV current) Biological
  • Fluzone®, licensed trivalent influenza vaccine (TIV) Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 31, 2012
Primary completion
Mar 31, 2013
Completion
Mar 31, 2013
Last update posted
Sep 10, 2025

2013

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
East Valley Family Physicians, PLC Chandler Arizona 85224
Anaheim Clinical Trials Anaheim California 92801
Center for Clinical Trials, LLC Paramount California 90723
California Research Foundation San Diego California 92103
Benchmark Research San Francisco San Francisco California 94102
Clinical Research of South Florida Coral Gables Florida 33134
Avail Clinical Research, LLC DeLand Florida 32720
Miami Research Associates South Miami Florida 33143
Clinical Research Atlanta Stockbridge Georgia 30281
Heartland Research Associates, LLC Wichita Kansas 67207
The Center for Pharmaceutical Research, P.C. Kansas City Missouri 64114
Sundance Clinical Research, LLC St Louis Missouri 63141
Rochester Clinical Research Inc. Rochester New York 14609
PMG Research of Cary, LLC Cary North Carolina 27518
Wake Research Associates, LLC Raleigh North Carolina 27612
Rapid Medical Research, Inc. Cleveland Ohio 44122
Spartanburg Medical Research Spartanburg South Carolina 29303
Benchmark Research Austin Austin Texas 78705
Benchmark Research Fort Worth Texas 76135
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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01773928, 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 10, 2025 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01773928 live on ClinicalTrials.gov.

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