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ID

23756

Beschrijving

Study part: Central Laboratory –Blood Week 20. A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Trefwoorden

  1. 12-07-17 12-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

12 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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    Central Laboratory –Blood Week 20 Mepolizumab HES NCT00086658

    Central Laboratory –Blood Week 20

    CENTRAL LABORATORY - BLOOD
    Beschrijving

    CENTRAL LABORATORY - BLOOD

    Alias
    UMLS CUI-1
    C1880016 (Central Laboratory)
    Subject Identifier
    Beschrijving

    Subject Identifier

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Date sample taken
    Beschrijving

    Date sample taken

    Datatype

    date

    Alias
    UMLS CUI [1]
    C1302413 (Specimen collection date)
    SNOMED
    399445004

    Similar models

    Central Laboratory –Blood Week 20

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    CENTRAL LABORATORY - BLOOD
    C1880016 (UMLS CUI-1)
    Subject Identifier
    Item
    Subject Identifier
    text
    C2348585 (UMLS CUI [1])
    Date sample taken
    Item
    Date sample taken
    date
    C1302413 (UMLS CUI [1])

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