drugset / Trial / NCT00254969

Immunogenicity and Safety of Pentaxim in South African Infants

NCT00254969

Phase 3 Completed 212 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelPrevention

Summary

The present clinical study will assess the immunogenicity and reactogenicity 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 in order to meet the requirements for application for the use of the product in the Expanded Program on Immunization (EPI) in South Africa.

Timeline

Start
2005-10
Primary completion
2008-05
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject PENTAXIM™ Vaccine 0.5 ml Intramuscular