Yearly Strain Variation Study, 2009/2010

NCT ID: NCT00943657

Last Updated: 2015-10-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 110 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-06-30
• Study Completion Date: 2009-07-31

Brief Summary

The purpose of this study is to verify the immunogenicity and tolerance of a trivalent seasonal influenza vaccine with strain composition according to World Heath Organization/European Union (WHO/EU) recommendation for the 2009/2010 season for yearly licensing application.

Conditions

Influenza; Seasonal Influenza

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Interventions

Preflucel [Trivalent seasonal influenza vaccine (split virus, Vero cell-derived)]

Single intramuscular injection of vaccine

Intervention Type: BIOLOGICAL

Other Intervention Names

Preflucel

Eligibility Criteria

Inclusion Criteria

• Subject is 18 to 59 years of age , inclusive, at the time of screening (for subjects in age stratum A only)
• Subject is 60 years of age or older , inclusive, at the time of screening (for subjects in age 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 female 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
• Subject is a member of the team conducting this study or is in a dependent relationship with one of the study team members. Dependent relationships include close relatives (ie, children, partner/spouse, siblings, parents) as well as employees of the investigator or site personnel conducting the study
• If female, subject is pregnant or lactating at the time of study enrollment

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Alachua Government Services, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Baxter Healthcare Corporation

Locations

Medical University of Vienna, Department of Clinical Pharmacology

Vienna, , Austria

Countries

Austria

Other Identifiers

720901

Identifier Type: -

Identifier Source: org_study_id