CLINICAL_TRIALS ClinicalTrials.gov record update

Open, Randomized, Phase II, Clinical Trial to Compare the Immunogenicity and Safety of a Booster Dose of GSK Biologicals' DTaP-IPV Vaccine (Infanrix®-IPV) Co-administered With a Booster Dose of Merck and Company's M-M-R®II, to That of Separate Injections of GSK Biologicals' DTaP Vaccine (Infanrix®), Aventis Pasteur's IPV (IPOL®) and M-M-R®II Administered as Booster Doses to Healthy Children 4 to 6 Years of Age.

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00263692
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:25.902214+00:00
Published At: 2016-09-15T00:00:00+00:00
Record Updated At: 2016-09-15
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Diphtheria", "Acellular Pertussis", "Tetanus"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2016-09-15"
protocolSection.identificationModule.nctId: "NCT00263692"
protocolSection.identificationModule.officialTitle: "Open, Randomized, Phase II, Clinical Trial to Compare the Immunogenicity and Safety of a Booster Dose of GSK Biologicals\u0027 DTaP-IPV Vaccine (Infanrix\u00ae-IPV) Co-administered With a Booster Dose of Merck and Company\u0027s M-M-R\u00aeII, to That of Separate Injections of GSK Biologicals\u0027 DTaP Vaccine (Infanrix\u00ae), Aventis Pasteur\u0027s IPV (IPOL\u00ae) and M-M-R\u00aeII Administered as Booster Doses to Healthy Children 4 to 6 Years of Age."
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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