Study of TAK-816 in Healthy Infants

PHASE3CompletedINTERVENTIONAL
Enrollment

416

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

February 28, 2013

Study Completion Date

February 28, 2013

Conditions
Immunization
Interventions
BIOLOGICAL

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.

BIOLOGICAL

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.

Trial Locations (22)

Unknown

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

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Takeda

INDUSTRY