Study ID

208355/125

Clinical Study ID

208355/125

Study Title A phase III, open, multicenter study of the safety of Infanrix® when administered as a booster dose at 15 to 18 months of age following primary immunization in studies 217744/084 and 217744/085 (Subjects from DTaP-HepB-IPV-084 and DTaP-HepB-IPV-085)
Clinicaltrials.gov Identifier
Sponsor GlaxoSmithKline
Collaborators N/A
Phase Phase 3
Study Recruitment Status Completed
Generic Name Diphtheria, Tetanus, Acellular Pertussis Vaccine Adsorbed
Trade Name Infanrix
Study Indication Acellular Pertussis; Diphtheria; Tetanus; acellular pertussis

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