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日本人乳幼児におけるDTaP-IPV/Hibワクチンの初回接種および追加接種とDTaP-IPVとHibワクチンの同時接種の比較

基本情報

NCT ID
NCT02274285
ステータス
完了
試験のフェーズ
第3相
試験タイプ
介入
目標被験者数
424
治験依頼者名
Sanofi

概要

Primary objective: * To demonstrate the non-inferiority in terms of seroprotection rates (Hib antigen (PRP), Diphtheria, Tetanus, and Pertussis antigens (PT and FHA), and polio types 1, 2 and 3 antigens) of investigational arm (Group A: DTaP-IPV/Hib) versus control arm (Group B: DTaP-IPV and Hib vaccines administered at separate sites), one month after the primary vaccination (all antigens). Secondary objectives: * To describe immune responses against all vaccine antigens with no pre-specified hypothesis, and at all time points (pre-dose 1, post-dose 3, pre-dose 4 and post-dose 4) in the two study groups (Group A and Group B). * To describe the safety after each dose of each vaccine in the two study groups (Group A and Group B). * To describe immune responses against all vaccine antigens with no pre-specified hypothesis, and at all time points (pre-dose 1, post-dose 3, pre-dose 4 and post-dose 4 (Group C)

対象疾患

TetanusDiphtheriaPertussisPoliomyelitisBacterial Meningitis

介入

DTaP-IPV/Hib Combined vaccine(BIOLOGICAL)
DTaP-IPV vaccine and Hib vaccine(BIOLOGICAL)
DTaP-IPV/Hib Combined vaccine(BIOLOGICAL)

依頼者(Sponsor)