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Comparison of the Immunogenicity and Safety of Three Consistency Lots of V260 in Healthy Infants
This study was designed to evaluate consistency in the antibody response to three manufactured lots of an investigational Rotavirus Vaccine.
Age
0 - 0 years
Sex
ALL
Healthy Volunteers
Yes
Start Date
May 1, 2003
Primary Completion Date
August 1, 2004
Completion Date
August 1, 2004
Last Updated
October 5, 2015
793
ACTUAL participants
rotavirus vaccine, live, oral, pentavalent
BIOLOGICAL
Placebo
BIOLOGICAL
Lead Sponsor
Merck Sharp & Dohme LLC
NCT06962904
NCT03483116
NCT02542462
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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