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A phase III randomized, double-blind, active-comparator controlled clinical trial to study the safety, tolerability, and immunogenicity of V419 in healthy infants when given at 2, 4, and 11 to 12 mont...

Mise à jour : Il y a 4 ans
Référence : EUCTR2010-021491-28

A phase III randomized, double-blind, active-comparator controlled clinical trial to study the safety, tolerability, and immunogenicity of V419 in healthy infants when given at 2, 4, and 11 to 12 months

Femme et Homme

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Extrait

To evaluate the immunogenicity of PR5I when given at 2, 4, and 11 to 12 months of age.

Critère d'inclusion

  • PR5I is developed to provide active immunization against diphtheria, tetanus, pertussis, poliomyelitis (caused by poliovirus Types 1, 2 and 3), invasive disease caused by Haemophilus influenza type b and infection caused by all known subtypes of hepatitis B virus

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