An Open-Label Phase 3 Study to Assess the Immunogenicity and Safety of a Vero Cell-Derived Trivalent Seasonal Influenza Vaccine, Strain Composition 2010/2011, in an Adult and Elderly Population

Resilience Government Services, Inc.1 site in 1 country110 target enrollmentJuly 2010

ConditionsInfluenza Seasonal Influenza

Overview

Phase: Phase 3
Intervention: Not specified
Conditions: Influenza
Sponsor: Resilience Government Services, Inc.
Enrollment: 110
Locations: 1
Primary Endpoint: To assess the immunogenicity to each of the three antigens contained in a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2010/2011 season in an adult and elderly population
Status: Completed
Last Updated: 5 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of the study is to verify the immunogenicity and tolerance of a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2010/2011 season for yearly licensing application.

Registry

clinicaltrials.gov

Start Date

July 2010

End Date

August 2010

Last Updated

5 years ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Resilience Government Services, Inc.

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Subject is 18 to 59 years of age, inclusive, at the time of screening (for Stratum A only)
•Subject is 60 years of age or older, inclusive, at the time of screening (for Stratum B only)
•Subject has given written informed consent prior to study entry
•Subject is generally healthy, as determined by the investigator's clinical judgment through collection of medical history and performance of a physical examination, such that the investigator would not hesitate to provide routine influenza immunization to the subject in the course of routine medical practice
•Subject agrees to keep a daily record of symptoms for the duration of the study
•If subject is of childbearing potential, subject presents with a negative urine pregnancy test, and agrees to employ adequate birth control measures for the duration of the study
•Subject is willing and able to comply with the requirements of the protocol

Exclusion Criteria

•Subject has a history of severe allergic reaction or anaphylaxis
•Subject has an oral temperature of \>= 37.5°C on the day of vaccination in this study.
•Subject has a rash or dermatologic condition or tattoos, which may interfere with injection site reaction rating
•Subject has received a live vaccine within 4 weeks or an inactivated or subunit vaccine within 2 weeks of study entry
•Subject has received a seasonal influenza vaccine within 6 months of study entry
•Subject currently has or had a history of a significant neurological, cardiovascular, pulmonary (including asthma), hepatic, metabolic, rheumatic, autoimmune, hematological or renal disorder
•Subject has any inherited or acquired immunodeficiency
•Subject has a disease or is currently undergoing a form of treatment or was undergoing a form of treatment within 30 days prior to study entry that can be expected to influence immune response. Such treatment includes, but is not limited to, systemic or high dose inhaled (\>800 µg/day of beclomethasone dipropionate or equivalent) corticosteroids, radiation treatment or other immunosuppressive or cytotoxic drugs.
•Subject has a functional or surgical asplenia
•Subject has a known or suspected problem with alcohol or drug abuse

Outcomes

Primary Outcomes

To assess the immunogenicity to each of the three antigens contained in a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2010/2011 season in an adult and elderly population

Time Frame: 1 month