Open-label, randomised, parallel-group, multicentre study to evaluate the safety, tolerability and immunogenicity of an AS03(B)/oil-in-water emulsion-adjuvanted (AS03(B)) split-virion versus non-adjuvanted whole-virion H1N1 influenza vaccine in UK children 6 months to 12 years of age.

Waddington, Cs

Open-label, randomised, parallel-group, multicentre study to evaluate the safety, tolerability and immunogenicity of an AS03(B)/oil-in-water emulsion-adjuvanted (AS03(B)) split-virion versus non-adjuvanted whole-virion H1N1 influenza vaccine in UK children 6 months to 12 years of age. [electronic resource] - Health technology assessment (Winchester, England) Oct 2010 - 1-130 p. digital

Publication Type: Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

2046-4924

10.3310/hta14460-01 doi


Antibodies, Viral--biosynthesis
Child
Child, Preschool
Disease Outbreaks--statistics & numerical data
Drug Combinations
Emulsions
Female
Humans
Immunization Programs
Infant
Influenza A Virus, H1N1 Subtype--immunology
Influenza Vaccines--administration & dosage
Influenza, Human--prevention & control
Male
Polysorbates--administration & dosage
Program Evaluation
Squalene--administration & dosage
United Kingdom
alpha-Tocopherol--administration & dosage