0 Evaluaciones

ID

22789

Descripción

Study part: Pharmacokinetics- Blood Week 4. 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

  1. 11/6/17 11/6/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

11 de junio de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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    Pharmacokinetics- Blood Week 4 Mepolizumab HES NCT00086658

    Pharmacokinetics- Blood Week 4

    PHARMACOKINETICS - BLOOD
    Descripción

    PHARMACOKINETICS - BLOOD

    Alias
    UMLS CUI-1
    C0031327
    UMLS CUI-2
    C0005767
    Subject Identifier
    Descripción

    Subject Identifier

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2348585
    Visit Date
    Descripción

    Visit Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1320303
    Planned Relative Time
    Descripción

    Planned Relative Time

    Tipo de datos

    time

    Alias
    UMLS CUI [1]
    C0439564
    Date Sample Taken
    Descripción

    Date Sample Taken

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1302413
    Actual Time
    Descripción

    Actual Time

    Tipo de datos

    time

    Alias
    UMLS CUI [1]
    C0040223
    Sample Identifier
    Descripción

    Sample Identifier

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C4071975

    Similar models

    Pharmacokinetics- Blood Week 4

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    PHARMACOKINETICS - BLOOD
    C0031327 (UMLS CUI-1)
    C0005767 (UMLS CUI-2)
    Subject Identifier
    Item
    Subject Identifier
    text
    C2348585 (UMLS CUI [1])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Planned Relative Time
    Item
    Planned Relative Time
    time
    C0439564 (UMLS CUI [1])
    Date Sample Taken
    Item
    Date Sample Taken
    date
    C1302413 (UMLS CUI [1])
    Actual Time
    Item
    Actual Time
    time
    C0040223 (UMLS CUI [1])
    Sample Identifier
    Item
    Sample Identifier
    text
    C4071975 (UMLS CUI [1])

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