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ID

33079

Description

Study ID: 104020 Clinical Study ID: 104020 Study Title: Blinded, randomised study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ live attenuated measles-mumps-rubella-varicella candidate vaccine when given to healthy children in their second year of life Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00126997 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Combined Measles, Mumps, Rubella, Varicella Vaccine Trade Name: Priorix Tetra Study Indication: Measles; Mumps; Rubella; Varicella

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Versions (1)
  1. 26/11/2018 26/11/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

26 novembre 2018

DOI

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Creative Commons BY-NC 3.0
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    Immunogenicity of Combined Measles, Mumps, Rubella, Varicella Vaccine for healthy 2 y.o children - 104020

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    Concomitant Vaccination Form

    1 Formulaires  
    Administrative data
    Description

    Administrative data

    Subject Number
    Description

    Subject Number

    Type de données

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    Concomitant Vaccination
    Description

    Concomitant Vaccination

    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the protocol?
    Description

    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the protocol?

    Type de données

    boolean

    If Yes, please record concomitant vaccination with trade name and /or generic name, route and vaccine administration date
    Description

    If Yes, please record concomitant vaccination with trade name and /or generic name, route and vaccine administration date

    Type de données

    text

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    Trade Name / Generic Name

    Trade / Generic Name
    Description

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    text

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    Route

    Type de données

    text

    Administration Date
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    Administration Date

    Type de données

    date

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    Concomitant Vaccination Form

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    Alias
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    Administrative data
    Subject Number
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    Concomitant Vaccination
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    Item
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the protocol?
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    If Yes, please record concomitant vaccination with trade name and /or generic name, route and vaccine administration date
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