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Japanese

Oct. 27, 2009

Dec. 17, 2018

jRCT2080220899

Phase II Clinical Study of DD-687 - Single arm, unblinded, uncontrolled Clinical Study in Healthy Japanese Infants -

version:
date:

DAIICHI SANKYO Co.,Ltd.

http://www.daiichisankyo.co.jp/corporate/rd/measure/clinical/index.html

110

Interventional

Prophylaxis

2

Aged 3 months to 8 months

>= 37.5°C (axillary temperature) on the day of inclusion. History of pertussis, diphtheria, tetanus, poliomyelitis infection.

No limit
No limit

Both

Prophylaxis of pertussis, diphtheria, tetanus, and poliomyelitis infection.

investigational material(s)
Generic name etc : DD-687
INN of investigational material :
Therapeutic category code : 631 Vaccines
Dosage and Administration for Investigational material : Subcutaneous injection

Safety, Immunogenicity

DAIICHISANKYO Co.,Ltd.
Kitasato -Daiichi Sankyo Vaccine Co., Ltd., Sanofi Pasteur Co., Ltd., Sanofi Pasteur SA

JapicCTI-090931

History of Changes

No Publication date
11 Dec. 17, 2018 (this page) Changes
10 July. 08, 2015 Detail Changes
9 July. 08, 2015 Detail Changes
8 July. 08, 2015 Detail Changes
7 July. 08, 2015 Detail Changes
6 Nov. 04, 2011 Detail Changes
5 Nov. 04, 2011 Detail Changes
4 Jan. 27, 2011 Detail Changes
3 Feb. 10, 2010 Detail Changes
2 Jan. 21, 2010 Detail Changes
1 Oct. 27, 2009 Detail