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Clinical Trial Summary

The purpose of this study is to assess the immunogenicity in terms of antibody response and the safety/reactogenicity in terms of solicited and unsolicited symptoms and serious adverse events following primary vaccination of Taiwanese infants with pneumococcal conjugate vaccine GSK 1024850A co-administered with a diphtheria, tetanus, acellular pertussis (DTPa)-combined vaccine and rotavirus vaccine in children during the first 6 months of life.


Clinical Trial Description

The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00533507
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date September 18, 2007
Completion date June 6, 2008

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