0 Evaluaciones

ID

22723

Descripción

Study part: Prednisone Stabilisation Dose Day 1 Pre-Infusion.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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    Prednisone Stabilisation Dose Day 1 Pre-Infusion Mepolizumab HES NCT00086658

    Prednisone Stabilisation Dose Day 1 Pre-Infusion

    PREDNISONE STABILISATION DOSE
    Descripción

    PREDNISONE STABILISATION DOSE

    Alias
    UMLS CUI-1
    C3174092 (Medication dose)
    LOINC
    LP116765-1
    UMLS CUI-2
    C0032952 (prednisone)
    SNOMED
    10312003
    Prednisone stabilisation dose in the Screening Corticosteriod Medition section recorded?
    Descripción

    dose prednisone

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3174092 (Medication dose)
    LOINC
    LP116765-1
    UMLS CUI [1,2]
    C0032952 (prednisone)
    SNOMED
    10312003

    Similar models

    Prednisone Stabilisation Dose Day 1 Pre-Infusion

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    PREDNISONE STABILISATION DOSE
    C3174092 (UMLS CUI-1)
    C0032952 (UMLS CUI-2)
    dose prednisone
    Item
    Prednisone stabilisation dose in the Screening Corticosteriod Medition section recorded?
    boolean
    C3174092 (UMLS CUI [1,1])
    C0032952 (UMLS CUI [1,2])

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