Study of Inactivated, Split-Virion Influenza Vaccine and Standard Fluzone® Vaccine in Adult and Elderly Subjects

PHASE2CompletedINTERVENTIONAL
Enrollment

2,098

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

June 30, 2008

Study Completion Date

November 30, 2008

Conditions
InfluenzaMyxovirus Infection
Interventions
BIOLOGICAL

Split, Inactivated, Trivalent Influenza Vaccine (Intradermal Formulation 1)

0.1 mL, Intradermal (ID)

BIOLOGICAL

Split, Inactivated, Trivalent Influenza Vaccine (Intradermal Formulation 2)

0.1 mL, Intradermal (ID)

BIOLOGICAL

Split, Inactivated, Trivalent Influenza Vaccine (Standard dose)

0.5 mL, Intramuscular (IM)

BIOLOGICAL

Split, Inactivated, Trivalent Influenza Vaccine (High-dose)

0.5 mL, Intramuscular (IM)

BIOLOGICAL

Split, Inactivated, Trivalent Influenza Vaccine (Standard dose)

0.5 mL, Intramuscular (IM)

Trial Locations (29)

Unknown

Alabaster

Mobile

Chandler

Mesa

Phoenix

Tucson

Fountain Valley

San Diego

Stanford

Pembroke Pines

Pinellas Park

Boise

Chicago

Wichita

Kansas City

Springfield

St Louis

Cary

Raleigh

Cincinnati

Allentown

Bensalem

Warwick

Goose Creek

Fort Worth

Galveston

Salt Lake City

West Jordan

Marshfield

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY