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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Immunogenicity of a Split, Cell-Based, Inactivated, Trivalent Influenza Vaccine in Healthy Adult Subjects

ClinicalTrials.gov ID: NCT00845429

Public ClinicalTrials.gov record NCT00845429. 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 27, 2026, 5:11 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

Immunogenicity of Two Dosages of a Split, Cell-Based, Inactivated, Trivalent Influenza Vaccine Administered in Healthy Adult Subjects Aged 18 to 49 Years

Brief summary

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

Primary Objective: To describe the immune response to a single administration of 2 formulations of the investigational cell-based influenza vaccines in healthy adult subjects. Secondary Objective: To describe the safety following a single administration of 2 formulations of the investigational cell-based influenza vaccines in healthy adult subjects.

Study identification

NCT ID
NCT00845429
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
729 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 49 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
Oct 2007 (Type not available)
Primary completion
Aug 2008 (Actual)
Completion
Nov 2008 (Actual)
Last update posted
Dec 19, 2012

2007 – 2008

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Not listed Hoover Alabama 35216 —
Not listed Mobile Alabama 36608 —
Not listed Tucson Arizona 85710 —
Not listed Milford Connecticut 06460 —
Not listed Pinellas Park Florida 33781 —
Not listed Chicago Illinois 60610 —
Not listed Wichita Kansas 67207 —
Not listed Kansas City Missouri 64114 —
Not listed Springfield Missouri 65802 —
Not listed Cary North Carolina 27518 —
Not listed Raleigh North Carolina 27609 —
Not listed Cincinnati Ohio 45249 —
Not listed Bensalem Pennsylvania 19020 —
Not listed Warwick Rhode Island 02886 —
Not listed Mt. Pleasant South Carolina 29464 —

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 NCT00845429, 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 Dec 19, 2012 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00845429 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →