0 Ratings
ID

23772

Description

Study part: Adverse Events Week 28. 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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Versions (1)
  1. 7/12/17 7/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 12, 2017

DOI

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Creative Commons BY-NC 3.0
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    Adverse Events Week 28 Mepolizumab HES NCT00086658

    English

    Adverse Events Week 28

    1 forms  
    1. StudyEvent: ODM
      1. Adverse Events Week 28
    ADVERSE EVENTS
    Description

    ADVERSE EVENTS

    Alias
    UMLS CUI-1
    C0877248
    Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
    Description

    Adverse Events

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0877248
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    Similar models

    Adverse Events Week 28

    1 forms
    1. StudyEvent: ODM
      1. Adverse Events Week 28
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    ADVERSE EVENTS
    C0877248 (UMLS CUI-1)
    Adverse Events
    Item
    Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
    boolean
    C0877248 (UMLS CUI [1])
    Back to the top of the page 

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