0 Evaluaciones

ID

22717

Descripción

Study part: Adverse Events Screening Visit.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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    Adverse Events Screening Visit Mepolizumab HES NCT00086658

    Adverse Events Screening Visit

    ADVERSE EVENTS
    Descripción

    ADVERSE EVENTS

    Alias
    UMLS CUI-1
    C0877248 (Adverse event)
    LOINC
    MTHU014542
    AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?
    Descripción

    Adverse Events

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0877248 (Adverse event)
    LOINC
    MTHU014542

    Similar models

    Adverse Events Screening Visit

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    ADVERSE EVENTS
    C0877248 (UMLS CUI-1)
    Adverse Events
    Item
    AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?
    boolean
    C0877248 (UMLS CUI [1])

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