416
Participants
Start Date
June 30, 2011
Primary Completion Date
February 28, 2013
Study Completion Date
February 28, 2013
TAK-816+ DPT-TAKEDA
TAK-816 0.5 mL and DPT-TAKEDA 0.5.mL, subcutaneous injections, three doses administered at 4-week intervals over 8 weeks, followed by a fourth dose 52 weeks after third dose.
ActHIB+ DPT-TAKEDA
ActHIB 0.5 mL and DPT-TAKEDA 0.5.mL, subcutaneous injections, three doses administered at 4-week intervals over 8 weeks, followed by a fourth dose 52 weeks after third dose.
Isumi
Urayasu-shi
Fukuoka
Itoshima-shi
Kasuga-shi
Hiroshima
Yokohama
Kumamoto
Tsu
Okayama
Kumagaya-shi
Shizuoka
Fuchu-shi
Koto-ku
Nishi-Tokyo-shi
Oota-ku
Setagaya-ku
Suginami-ku
Tachikawa-shi
Tama-shi
Kofu
Tsuru-shi
Lead Sponsor
Takeda
INDUSTRY