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Clinical Trial Summary

This study will determine whether participants who receive V419 (PR5I) at 2, 4, and 11 to 12 months of age have an acceptable response to the vaccine. This study will also determine whether the immune response to V419 is similar to that of participants who received a licensed vaccine control. The primary hypothesis is that participants who receive PR5I at 2, 4, and 11 to 12 months have an acceptable response rate to all PR5I-contained antigens at one month after the Toddler dose of PR5I.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01480258
Study type Interventional
Source MCM Vaccines B.V.
Contact
Status Completed
Phase Phase 3
Start date November 23, 2011
Completion date October 9, 2013

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