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Clinical Trial Summary

A study to compare safety, tolerability, and immunogenicity of a new formulation of RotaTeq™ with the existing formulation in infants. The primary hypothesis of the study is that the new formulation will be noninferior to the existing formulation on the basis of immunogenicity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01600092
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 3
Start date April 29, 2013
Completion date March 25, 2014

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