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Completed Phase 2 Interventional Accepts healthy volunteers

Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >= 18 and <= 64, Plus Revaccination

ClinicalTrials.gov ID: NCT00889889

Public ClinicalTrials.gov record NCT00889889. 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 Oct 29, 2026, 11:45 AM 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, Double-Blind, Placebo-Controlled Study to Assess the Immunogenicity and Safety of a Cell-Derived Trivalent Subunit Influenza Vaccine in Subjects Aged >= 18 Years and <= 64 Years During Two Consecutive Years.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Immunogenicity and safety of a cell-derived influenza vaccine in adults aged \>= 18 and \<= 64 years, plus revaccination

Study identification

NCT ID
NCT00889889
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott Biologicals
Industry
Enrollment
1,270 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 64 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
May 2009 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Jan 2011 (Actual)
Last update posted
Oct 25, 2013

2009 – 2011

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Site Reference ID/Investigator# 45690 Jacksonville Florida 32216 —
Site Reference ID/Investigator# 45687 Pembroke Pines Florida 33024 —
Site Reference ID/Investigator# 45697 South Miami Florida 33143 —
Site Reference ID/Investigator# 45691 Lenexa Kansas 66219 —
Site Reference ID/Investigator# 45689 Overland Park Kansas 66212 —
Site Reference ID/Investigator# 45694 Wichita Kansas 67207 —
Site Reference ID/Investigator# 45682 Lexington Kentucky 40509 —
Site Reference ID/Investigator# 45684 Kansas City Missouri 64114 —
Site Reference ID/Investigator# 45685 Omaha Nebraska 68134 —
Site Reference ID/Investigator# 45686 Las Vegas Nevada 89104 —
Site Reference ID/Investigator# 45688 Raleigh North Carolina 27612 —
Site Reference ID/Investigator# 45696 Nashville Tennessee 37203 —
Site Reference ID/Investigator# 45683 Austin Texas 78705 —
Site Reference ID/Investigator# 45695 Fort Worth Texas 76135 —
Site Reference ID/Investigator# 45692 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 NCT00889889, 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 Oct 25, 2013 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00889889 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →