0 Evaluaciones
ID

36624

Descripción

Study ID: 102394 Clinical Study ID: 102394 Study Title: A Phase IV, partially double-blind study to demonstrate non-inferiority of GSK Biologicals’ Mencevax™ ACWY (new process) versus Mencevax™ ACWY (current process) when administered as a single dose to subjects aged 2-30 yrs Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00227422 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed clinical study under GSK sponsorship. The product that is studied in this clinical study, together with the rights to the data and results generated, has been transferred by GSK to Pfizer. GSK’s Clinical Study Register is no longer maintained for this study. To request access to clinical study data from Pfizer, go here: http://www.pfizer.com/research/clinical_trials/trial_data_and_results Generic Name: Meningococcal Serogroups A, C, W-135 and Y Vaccine Trade Name: Mencevax Study Indication: Infections, Meningococcal

Link

http://www.pfizer.com/research/clinical_trials/trial_data_and_results

Palabras clave

Versiones (1)
  1. 26/5/19 26/5/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

26 de mayo de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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    Mencevax™ ACWY (new process) versus Mencevax™ ACWY (current process); NCT00227422

    Inglés

    Concomitant Vaccination

    1 formularios  
    Administrative Data
    Descripción

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Descripción

    Clinical Trial Subject Unique Identifier

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Concomitant Vaccination
    Descripción

    Concomitant Vaccination

    Alias
    UMLS CUI-1
    C2347852
    UMLS CUI-2
    C0042196
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
    Descripción

    Concomitant Agent, Vaccination

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0042196
    Trade / (Generic) Name
    Descripción

    Concomitant Agent, Vaccination, Medication name

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0042196
    UMLS CUI [1,3]
    C2360065
    Route
    Descripción

    Concomitant Agent, Vaccination, Drug Administration Routes

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0042196
    UMLS CUI [1,3]
    C0013153
    Administration date
    Descripción

    Concomitant Agent, Vaccination, Date in time

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0042196
    UMLS CUI [1,3]
    C0011008
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    Similar models

    Concomitant Vaccination

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Number
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Concomitant Vaccination
    C2347852 (UMLS CUI-1)
    C0042196 (UMLS CUI-2)
    Concomitant Agent, Vaccination
    Item
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
    boolean
    C2347852 (UMLS CUI [1,1])
    C0042196 (UMLS CUI [1,2])
    Concomitant Agent, Vaccination, Medication name
    Item
    Trade / (Generic) Name
    text
    C2347852 (UMLS CUI [1,1])
    C0042196 (UMLS CUI [1,2])
    C2360065 (UMLS CUI [1,3])
    Concomitant Agent, Vaccination, Drug Administration Routes
    Item
    Route
    text
    C2347852 (UMLS CUI [1,1])
    C0042196 (UMLS CUI [1,2])
    C0013153 (UMLS CUI [1,3])
    Concomitant Agent, Vaccination, Date in time
    Item
    Administration date
    date
    C2347852 (UMLS CUI [1,1])
    C0042196 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
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