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Immunogenicity, Reactogenicity and Safety Study of Pediarix®, Hiberix® and Prevenar 13® Co-administered With Two Different Formulations of GSK Biologicals' HRV Vaccine (444563) in Healthy Infants 6-12 Weeks of Age

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03207750
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:53.160189+00:00
Published At
2019-10-31T00:00:00+00:00
Record Updated At
2020-12-29
Results Posted At
2019-10-31
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Rotavirus Infection", "Rotavirus Vaccines"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2020-12-29"
protocolSection.identificationModule.nctId
"NCT03207750"
protocolSection.identificationModule.officialTitle
"Immunogenicity, Reactogenicity and Safety Study of Pediarix\u00ae, Hiberix\u00ae and Prevenar 13\u00ae Co-administered With Two Different Formulations of GSK Biologicals\u0027 HRV Vaccine (444563) in Healthy Infants 6-12 Weeks of Age"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2019-10-31"

Study condition terms

  • Rotavirus Infection (protocolSection.conditionsModule.conditions)
  • Rotavirus Vaccines (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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