The present clinical study will assess the immunogenicity and reactogenicity of Sanofi Pasteur's DTacP-IPV// PRP\~T combined vaccine (Pentavac™ or Pentaxim™) as a three-dose primary vaccination at 2, 4, and 6 months of age followed by a booster dose during the second year of life and concomitant hepatitis B vaccine at 2 and 6 months of age in infants in Thailand.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
186
0.5 mL, IM
Unnamed facility
Bangkok, Thailand
Immunogenicity: To provide information concerning the immune response of the DTacP-IPV//PRP~T combined vaccine
Time frame: 1 month post-vaccination
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