ID

23756

Description

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.

Keywords

Versions (1)
  1. 2017-07-12 2017-07-12 -
Copyright Holder

GlaxoSmithKline

Uploaded on

12 juli 2017

DOI

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License

Creative Commons BY-NC 3.0
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    Central Laboratory –Blood Week 20 Mepolizumab HES NCT00086658

    English

    Central Laboratory –Blood Week 20

    1 forms  
    CENTRAL LABORATORY - BLOOD
    Description

    CENTRAL LABORATORY - BLOOD

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

    Subject Identifier

    Data type

    text

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

    Date sample taken

    Data type

    date

    Alias
    UMLS CUI [1]
    C1302413 (Specimen collection date)
    SNOMED
    399445004
    Back to the top of the page

    Similar models

    Central Laboratory –Blood Week 20

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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])
    Back to the top of the page 

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