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A Phase 4, Open-label Study to Evaluate Persistence of the Antibody Response Elicited by Prevenar in Healthy Children in China Who Have Been Previously Immunized With a 4-dose Series of a Pneumococcal Conjugate Vaccine During Infancy in Study 0887x-101518
In 2005, Wyeth conducted study 0887X-101518 (NCT00488826) in which Chinese infants received either Prevenar alone (Group 1), Prevenar given with a Diphtheria, Tetanus and acellular Pertussis (DTaP) vaccine (Group 2) or DTaP alone (Group 3). This follow up study (at least 3 years after the last vaccination) will assess the antibody concentrations in children who previously completed Wyeth study 0887X-101518.
Age
4 - 5 years
Sex
ALL
Healthy Volunteers
Yes
Chengxiang Town Hospital
Longan County, Guangxi, China
Longan County CDC
Longan County, Guangxi, China
Nanyu Town Hospital
Longan County, Guangxi, China
Yanjiang Town Hospital
Longan County, Guangxi, China
Natong Town Hospital
Longan County, Guangxi, China
Qiaojian Town Hospital
Longan County, Guangxi, China
Gutan Village Hospital
Longan County, Guangxi, China
Dingdang Town Hospital
Longan County, Guangxi, China
Yangwan Hospital
Longan County, Guangxi, China
GuangXi Center for Disease Prevention and Control
Nanning, Guangxi, China
Start Date
November 1, 2010
Primary Completion Date
March 1, 2011
Completion Date
March 1, 2011
Last Updated
December 19, 2018
335
ACTUAL participants
Blood draw
PROCEDURE
Lead Sponsor
Pfizer
NCT06731374
NCT06044077
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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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View ClinicalTrials.gov Terms and ConditionsNCT06790290