A Phase 3 interventional study of Diphtheria, Tetanus, Polio, Acellular Pertussis and Hib in Diphtheria, Tetanus and Haemophilus Infections, sponsored by Sanofi. Completed at 1 site in South Africa. Open to participants aged 24 Hours and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-04-17.
Sponsored by Sanofi · Phase 3, Interventional, and Prevention
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.
238 studies on the registry are indexed under Whooping Cough; 15 are open to participants now.
This study's enrollment of 212 is below the median of 375 across 180 interventional studies indexed under Whooping Cough.
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Exclusion Criteria:
Biological: Diphtheria, Tetanus, Polio, Acellular Pertussis and Hib
0.5 mL, Im
Also known as: PENTAXIM™
To provide information concerning the immunogenicity of DTacP-IPV//PRP~T combined vaccine.
Time frame: 1 month post-vaccination
This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.
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Sanofi