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Clinical Trials associated with Diphtheria,tetanus and acellular pertussis combined Vaccine,adsorbed(Sanofi Pasteur)Immunogenicity and Safety of Pentaxim as 3 Doses Primary Vaccination Followed by a Booster Dose at 18 Months
As per request by the Heath Authorities, the present clinical study will assess the immunogenicity and safety of sanofi pasteur's DTacP-IPV// PRP
T combined vaccine (PENTAXIM™) as a three-dose primary vaccination at 2, 3, and 4 months of age or 3, 4 and 5 months of age followed by a booster dose at 18-20 months of age as compared to commercially available DTacP, Hib conjugate (Act-HIB™) and IPV (IMOVAX Polio™) monovalent vaccines in order to meet the requirements for registration of the product in People's Republic of China.
Immunogenicity and Safety of Pentaxim in South African Infants
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.
100 Clinical Results associated with Diphtheria,tetanus and acellular pertussis combined Vaccine,adsorbed(Sanofi Pasteur)
100 Translational Medicine associated with Diphtheria,tetanus and acellular pertussis combined Vaccine,adsorbed(Sanofi Pasteur)
100 Patents (Medical) associated with Diphtheria,tetanus and acellular pertussis combined Vaccine,adsorbed(Sanofi Pasteur)
100 Deals associated with Diphtheria,tetanus and acellular pertussis combined Vaccine,adsorbed(Sanofi Pasteur)