Pertussis Clinical Trial
Official title:
Phase 1 Extension Study to Evaluate Antibody Persistence Approximately 3 Years After Administration of Different Dosages of Acellular Pertussis or Tetanus-Diphtheria-acellular Pertussis Booster Vaccines in Healthy Adult Subjects Enrolled in Study V113_01
The purpose of this study is to evaluate the persistence of immune response against the
three pertussis antigens (anti- pertussis toxoid (PT), anti-filamentous hemagglutinin (FHA)
and anti-pertactin (PRN)) in subjects who received a booster dose of either aP or Tdap study
vaccines or Boostrix® during V113_01 study.
There was only one Clinic Visit at day 1. Eligible subjects went undergo a single blood draw
after which they were observed for approximately 15 minutes. Approximately 10.0 mL of blood
was withdrawn.
No vaccine was administered and no safety data was collected in this study.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
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