Tetanus Clinical Trial
Official title:
An Open, Multicentric, Post-marketing Surveillance Study to Assess the Safety and Reactogenicity of GlaxoSmithKline Biologicals' DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 and 18 Months of Age, in Healthy Infants.
To assess the safety and reactogenicity of the DTPa-IPV/Hib vaccine as primary and booster
vaccination. The DTPa-IPV/Hib vaccine given at 3 and 4 months of age is co-administered with
GSK Biologicals' rotavirus vaccine or Placebo.
The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep
2007.
Single group study. Subjects in GSK Biologicals' rotavirus study (Rota-028) in Singapore will be enrolled in this study. 3-4-5 month schedule with a booster dose at 18 months ;
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