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A phase IIIa open, randomised, controlled study to assess the safety, reactogenicity and immunogenicity induced by a booster dose of GlaxoSmithKline (GSK) Biologicals 10-valent pneumococcal conjugate ...

Mise à jour : Il y a 4 ans
Référence : EUCTR2006-001934-42

A phase IIIa open, randomised, controlled study to assess the safety, reactogenicity and immunogenicity induced by a booster dose of GlaxoSmithKline (GSK) Biologicals 10-valent pneumococcal conjugate vaccine when co-administered with GSK Biologicals’ measles-mumps-rubella-varicella vaccine (MMRV) vaccine in children during their second year of life, previously vaccinated in infancy in the primary study 10PN-PD-DIT-001 (105553) with GSK Biologicals 10-valent pneumococcal conjugate vaccine

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Extrait

• To assess the incidence of post-immunization rectal fever >39.0°C following a booster dose of GSK Biologicals’ 10-valent pneumococcal conjugate vaccine, when co-administered with the first dose of MMRV vaccine in children 12 to 14 months of age.

Critère d'inclusion

  • Booster vaccination against Streptococcus pneumoniae and active immunization against measles, mumps, rubella and varicella diseases in children during the second year of life

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