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Influenza

Clinical Study to Evaluate Safety, Immunogenicity of Investigational Flu Vaccine Compared to an Approved Flu Vaccine in Children Previously Vaccinated in Trial V118_05 (NCT01964989)
NCT02583256 | PHASE 3 | INTERVENTIONAL

Safety, Immunogenicity of an Adjuvanted Quadrivalent Subunit Influenza Virus Vaccine Compared to Non-Adjuvanted Comparator Influenza Vaccine in Children Previously vaccinated in Trial V118_05. Subjects will receive either the Same or Alternate Type of Vaccine.

Trial Information
17 Sites
1601 Participants
Recruiting
12 Months to 7 Years

If interested, contact clinicaltrials@cslbehring.com for more information

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Investigational Site
Espoo,Etelä-Suomen Lääni,Finland,02230
Investigational Site
Helsinki,Etelä-Suomen Lääni,Finland,00100
Investigational Site
Helsinki,Etelä-Suomen Lääni,Finland,00100
Investigational Site
Järvenpää,Etelä-Suomen Lääni,Finland,04400
Investigational Site
Kokkola,Länsi-Suomen Lääni,Finland,67100
Investigational Site
Pori,Länsi-Suomen Lääni,Finland,28100
Investigational Site
Tampere,Länsi-Suomen Lääni,Finland,33100
Investigational Site
Turku,Länsi-Suomen Lääni,Finland,20520
Investigational Site
Oulu,Finland,90220
Investigational Site
Laguna,Matro Manila,Philippines,1781
Investigational Site
Muntinlupa,National Capital Region,Philippines,1781
Investigational Site
Muntinlupa,National Capital Region,Philippines,1781
Investigational Site
Cavite,Philippines,4114
Investigational Site
Pathum Thani,Bangkok,Thailand,12120
Investigational Site
Bangkok,Krung Thep Maha Nakhon [Bangko,Thailand,10400
Investigational Site
Bangkok,Samut Prakan,Thailand,10400
Investigational Site
Bangkok,Thailand,10330

Study Eligibility Criteria

Additional Studies

Additional studies can be found at ClinicalTrials.gov