0 Evaluaciones
ID

22458

Descripción

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.

Palabras clave

Versiones (1)
  1. 5/6/17 5/6/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

5 de junio de 2017

DOI

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Licencia

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

    Inglés

    Status of treatment blind

    1 formularios  
    STATUS OF TREATMENT BLIND
    Descripción

    STATUS OF TREATMENT BLIND

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

    Study ID

    Tipo de datos

    text

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

    Status of treatment blind

    Tipo de datos

    boolean

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

    date Blinded Clinical Study

    Tipo de datos

    date

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

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

    Tipo de datos

    text

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

    Other

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0205394
    Volver a la parte superior de la página

    Similar models

    Status of treatment blind

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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])
    Volver a la parte superior de la página 

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