Seasonal Influenza
Conditions
Keywords
Influenza vaccine
Brief summary
Annual trial for registration influenza vaccine with the strain composition for season 2008/2009
Interventions
BIOLOGICALInfluenza Vaccine, Formulation 2008-2009
1 dose of Surface Antigen, Inactivated, Influenza Vaccine, Formulation 2008-2009
Sponsors
Novartis Vaccines
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Subjects eligible for enrollment into this study are male and female adults who are: 1. ≥ 18 years of age, mentally competent, willing and able to give informed consent prior to study entry 2. able to comply with all study requirements 3. in good health as determined by: * medical history * physical examination * clinical judgment of the investigator
Exclusion criteria
* They have any serious chronic or acute disease (in the judgment of the investigator) 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. * They have 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, kanamycin and neomycin sulphate); * They have a 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: * 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; * receipt of immunostimulants; * receipt of parenteral immunoglobulin preparation, blood products and/or plasma derivates within the past 3 months and for the full length of the study; * suspected or known HIV infection or HIV-related disease; * They have a known or suspected history of drug or alcohol abuse; * They have 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 women able to bear children but not willing to practice acceptable contraception for the duration of the trial (21 days); * Within the past 12 months, they have: * received more than one injection of influenza vaccine * Within the past 6 months, they have: * had laboratory confirmed influenza disease; * received influenza vaccine; * Within the past 4 weeks they have received: * another vaccine; * any investigational agent; * They have any acute or chronic infection requiring systemic antibiotic treatment or antiviral therapy within the last 7 days; 1 - They have experienced an acute exacerbation of a COPD within the past 14 days
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of antibody response to each influenza vaccine antigen, as measured by Single Radial Hemolysis (SRH) test on Day 0 and on Day 21 | 21 days (-1/+5) |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of safety | 21 days (-1/+5) |
Countries
Italy
Outcome results
None listed