Tetanus Clinical Trial
Official title:
Immunogenicity and Safety of the Sanofi Pasteur DTacP-IPV//PRP~T Combined Vaccine (PENTAXIM™) Given as a Three-Dose Primary Vaccination at 6, 10, and 14 Weeks of Age and Followed by a Booster Dose at 18-19 Months of Age in Healthy Infants in India.
The present clinical study will assess the immunogenicity as the primary objective and the
reactogenicity as the secondary objective of Aventis Pasteur's DTacP-IPV// PRP~T combined
vaccine (Pentavac™ or Pentaxim™) as a three-dose primary vaccination at 6, 10 and 14 weeks
of age followed by a booster dose during the second year of life.
Safety:
This study will describe the safety after each dose of the primary series of the study's
combined vaccine (Pentaxim™).
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
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