Pandemic Influenza
Conditions
Keywords
Pandemic influenza vaccine
Brief summary
This present study, randomized, single-blind, dose-ranging, multicenter study, will evaluate immunogenicity, safety and tolerability of two doses of an adjuvanted and not-adjuvanted new swine-origin influenza A/H1N1 virus monovalent subunit vaccine in healthy adult and elderly subjects. A booster dose will be administered 12 months after the first vaccination.
Interventions
BIOLOGICALMonovalent A/H1N1 influenza vaccine
This trial will be performed at multiple study sites in a population of healthy adults and elderly. Subjects will be randomized to receive two IM injections of low dose of antigen & adjuvant, or high dose of antigen & adjuvant, or high dose of antigen, according to the study groups.
Sponsors
Novartis Vaccines
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Males and females 18 years of age and above on the day of enrollment; 2. Individuals in good health 3. Individuals are able to comply with all study procedures 4. Willingness to allow for serum samples to be stored beyond the study period, for potential additional future testing to better characterize immune response.
Exclusion criteria
1. Individual not able to comprehend and to follow all required study procedures; 2. History or any illness that might interfere with the results of the study or pose additional risk to the subjects due to participation in the study; 3. Any serious chronic or progressive disease according to judgment of the investigator 4. History of any anaphylaxis, serious vaccine reactions, to any excipients. 5. Adjuvanted influenza vaccine or documented confirmed or suspected influenza disease within 3 months prior to Day 1; 6. Receipt of another investigational agent within 4 weeks prior to enrollment, or before completion of the safety follow-up period in this or in another study; unwilling to refuse participation in another clinical study through the end of this study; 7. Any other vaccines within 4 weeks prior to enrollment or who are planning to receive any vaccine within 4 weeks from the study vaccines; only exception being plain seasonal influenza vaccines which are allowed until 1 week prior to and after 1 week study vaccinations. 8. Receipt of blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation in the past 12 weeks; 9. Axillary temperature ≥ 38°C or oral temperature ≥ 38.5°C within 3 days of intended study vaccination; 10. Known or suspected impairment/alteration of immune function, for example resulting from a receipt of immunosuppressive therapy within 60 days prior to Visit 1; 11. History of progressive or severe neurological disorders; 12. Surgery planned during the study period that in the Investigator's opinion would interfere with the study visits schedule; 13. Female of childbearing potential, not used any acceptable contraceptive methods for at least 2 months prior to study entry; 14. Female pregnant or nursing (breastfeeding) mothers or females of childbearing potential do not plan to use acceptable birth control measures during the first 3 weeks after vaccination; 15. Members of the research staff or their relatives.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To identify the preferred vaccine formulation, dosage (antigen & adjuvant), schedule (one or two administrations) of the H1N1 sw monovalent vaccine in adults. | 43 days after first vaccination |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate immunogenicity against A/California H1N1sw strain after booster dose of egg-derived seasonal trivalent, MF59 adjuvanted vaccine Fluad, recommended for 2010/2011 season, administered 12 months after primary course according to CHMP criteria. | 3 weeks after booster vaccination |
Countries
Belgium, Germany, Switzerland
Outcome results
None listed