Infections, Rotavirus Clinical Trial
Official title:
Primary Vaccination Course in Children Receiving the Pneumococcal Vaccine GSK 1024850A, Infanrix Hexa and Rotarix
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.
The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007. ;
Status | Clinical Trial | Phase | |
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Completed |
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Phase 3 | |
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Phase 2 | |
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Completed |
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N/A | |
Completed |
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Completed |
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Completed |
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Phase 3 | |
Completed |
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Phase 2 | |
Completed |
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Completed |
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Phase 4 | |
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Phase 2 | |
Completed |
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Phase 2 | |
Completed |
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N/A | |
Completed |
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N/A | |
Completed |
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N/A |