Safety and Immunogenicity of Influenza Vaccine (Surface Antigen, Inactivated) Ph.Eur, Formulation 2008-2009, When Administered to Non-Elderly Adult and Elderly Subjects

NCT ID: NCT00748150

Last Updated: 2012-01-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 143 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-07-31
• Study Completion Date: 2008-08-31

Brief Summary

Annual trial for registration influenza vaccine with the strain composition for season 2008/2009

Detailed Description

At enrolment, subjects were stratified into two age strata (18 to 60 years, over 60 years). Total duration of the study is three weeks. Vaccinations were to be administered on day 1. Blood samples were collected at day 1 (baseline, before the vaccination) and at day 22 (three weeks after the vaccination). Sera were tested by Hemagglutination Inhibition (HI) assay. Safety was assessed until 3 weeks after the vaccination.

Conditions

Influenza

Study Design

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

Study Groups

1

Group Type: EXPERIMENTAL

Flu Vaccine Influenza Vaccine (Surface Antigen, Inactivated) Ph.Eur, Formulation 2008-2009

Intervention Type: BIOLOGICAL

1 dose, 0.5 mL of Flu Vaccine Influenza Vaccine (Surface Antigen, Inactivated) Ph.Eur, Formulation 2008-2009

Interventions

Flu Vaccine Influenza Vaccine (Surface Antigen, Inactivated) Ph.Eur, Formulation 2008-2009

1 dose, 0.5 mL of Flu Vaccine Influenza Vaccine (Surface Antigen, Inactivated) Ph.Eur, Formulation 2008-2009

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• ≥ 18 years of age, mentally competent, willing and able to give informed consent prior to study entry
• available for all the visits scheduled in the study and able to comply with all study requirements
• in good health as determined by:

1. medical history

2. physical examination

3. clinical judgment of the investigator

Exclusion Criteria

• Any serious (in the judgment of the investigator) disease including, but not limited to:

1. Cancer, except for localized skin cancer

2. Advanced congestive heart failure

3. Chronic obstructive pulmonary disease (COPD

4. Autoimmune disease (including rheumatoid arthritis)

5. Acute or progressive hepatic disease

6. Acute or progressive renal disease

7. Severe neurological or psychiatric disorder

8. Severe asthma

• History of any anaphylactic reaction and/or serious allergic reaction following a vaccination, a proven hypersensitivity to any component of the study vaccine (e.g. to ovalbumin, chicken protein, chicken feathers, influenza viral protein, neomycin, polymixin)
• Known or suspected (or have a high risk of developing) impairment/alteration of immune function (excluding that normally associated with advanced age) resulting for example from:

1. Receipt of immunosuppressive therapy (any parenteral or oral corticosteroid or cancer chemotherapy/radiotherapy) within the past 60 days and for the full length of the study

2. Receipt of immunostimulants,

3. Receipt of parenteral immunoglobulin preparation, blood products, and/or plasma derivatives within the past 3 months and for the full length of the study,

4. Suspected or known HIV infection or HIV-related disease.

• Known or suspected history of drug or alcohol abuse.
• The subject has a bleeding diathesis or condition associated with prolonged bleeding time that in the investigator's opinion would interfere with the safety of the subject
• Women who are pregnant or woman of child-bearing potential unwilling to practice acceptable contraception for the duration of the study (21 days).
• Influenza vaccination or laboratory confirmed influenza within the last 6 months and more than one influenza vaccination within the past 12 months
• Within the past 4 weeks, the subject has received:

1. another vaccine

2. any investigational agent

• Any acute or chronic infection requiring systemic antibiotic treatment or antiviral therapy within the last 7 days.
• The subject has experienced an acute exacerbation of a COPD within the past 14 days
• The subject has experienced fever (i.e. axillary temperature ³ 38.0°C) within the last 3 days
• Severely obese with Body Mass Index (BMI) > 35 kg/m2
• Any condition, which, in the opinion of the investigator, might prevent the subject from participation or interfere with the evaluation of the study objectives.

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

Sponsors

Novartis Vaccines

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Novartis Vaccines

Role: STUDY_CHAIR

Novartis Vaccines

Locations

The Health Centre

Heath Road, Woolpit, Bury Saint Edmunds, Suffolk, United Kingdom

Countries

United Kingdom

Other Identifiers

2008-000939-17

Identifier Type: -

Identifier Source: secondary_id

V78P6S

Identifier Type: -

Identifier Source: org_study_id