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Clinical Trial Summary

The purpose of this study is to assess the immunogenicity and safety of the Infanrix hexa booster dose given at 11-18 months of age to infants who received primary vaccination at 6-14 weeks. All infants in this booster study were born to pregnant women who participated in the study 116945 [DTPA (BOOSTRIX)-047] and having received the full primary vaccination series as per protocol requirement in study 201330 [DTPA (BOOSTRIX)-048.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02853929
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date September 19, 2016
Completion date March 19, 2019

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