Inactivated influenza vaccine (split virion) NH 2007-2008 formulation
Biological0.5 mL, Intramuscular
Other names: Vaxigrip
NCT Number: NCT00491257
This study is designed to generate clinical data as outlined in the Note for Guidance on harmonization requirements for influenza vaccine marketing authorization by the European Medicines Agency.
The objectives of the trial are:
* To determine immunogenicity, of the inactivated, split-virion influenza vaccine Northern Hemisphere (NH) 2007-2008 formulation in terms of the requirements of the Committee for Human Medicinal Products (CHMP) Note for Guidance (NfG) CPMP/BWP/214/96. * To describe the safety of the inactivated, split-virion influenza vaccine, NH 2007-2008 formulation.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Edinburgh, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.5 mL, Intramuscular
Other names: Vaxigrip
Time frame: 21 Days post-vaccination
Sanofi Pasteur, a Sanofi Company
Industry
Immunogenicity and Safety of the Inactivated, Split-Virion Influenza Vaccine, Northern Hemisphere 2007-2008 Formulation (Intramuscular Route)
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