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Study ID

100406/004

Study Title A phase III, double-blinded, randomized, multicenter, clinical study to assess the safety and immunogenicity of GSK Biologicals' Tdap 0.3 mg candidate vaccine when given as a booster dose to healthy school children and adolescents (9-13 years of age), previously vaccinated with a 5th consecutive dose of acellular pertussis-containing vaccine, in studies APV-118 or APV-120
Clinicaltrials.gov Identifier NCT00263679
Sponsor GlaxoSmithKline
Collaborators N/A
Study Recruitment Status Completed
Generic Name Combined Reduced Antigen Content Diphtheria, Tetanus, Acellular Pertussis Vaccine
Trade Name Boostrix
Study Indication Diphtheria; Tetanus; acellular pertussis