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ID

22458

Beschrijving

Study part: Status of treatment blind.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.

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  1. 05-06-17 05-06-17 -
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GlaxoSmithKline

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5 juni 2017

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Creative Commons BY-NC 3.0
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    Status of treatment blind Mepolizumab HES NCT00086658

    Engels

    Status of treatment blind

    1 Formulieren  
    STATUS OF TREATMENT BLIND
    Beschrijving

    STATUS OF TREATMENT BLIND

    Alias
    UMLS CUI-1
    C0749659
    UMLS CUI-2
    C2347038
    Study ID
    Beschrijving

    Study ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2826693
    Was the treatment blind broken during the study?
    Beschrijving

    Status of treatment blind

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0749659
    UMLS CUI [1,2]
    C2347038
    Date blind broken
    Beschrijving

    date Blinded Clinical Study

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C2347038
    Reason blind broken
    Beschrijving

    Complete Non-Serious Adverse Event, Serious Adverse Event and/or Investigational Product pages, as appropriate.

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C2347038
    If other, please specify
    Beschrijving

    Other

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0205394
    Terug naar het begin van de pagina

    Similar models

    Status of treatment blind

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    STATUS OF TREATMENT BLIND
    C0749659 (UMLS CUI-1)
    C2347038 (UMLS CUI-2)
    Study ID
    Item
    Study ID
    text
    C2826693 (UMLS CUI [1])
    Status of treatment blind
    Item
    Was the treatment blind broken during the study?
    boolean
    C0749659 (UMLS CUI [1,1])
    C2347038 (UMLS CUI [1,2])
    date Blinded Clinical Study
    Item
    Date blind broken
    date
    C0011008 (UMLS CUI [1,1])
    C2347038 (UMLS CUI [1,2])
    Item
    Reason blind broken
    text
    C0392360 (UMLS CUI [1,1])
    C2347038 (UMLS CUI [1,2])
    Reason
    Code List
    Reason blind broken
    CL Item
    Medical emergency requiring identification of investigational product for further treatment (Medical emergency requiring identification of investigational product for further treatment)
    CL Item
    Other, specify (Other, specify)
    Other
    Item
    If other, please specify
    text
    C0205394 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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