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ID

23831

Beschrijving

Study part: Adverse Events Week 38/ Early Withdrawal 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.

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Versies (1)
  1. 15-07-17 15-07-17 -
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GlaxoSmithKline

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15 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Adverse Events Week 38 Mepolizumab HES NCT00086658

    Engels

    Adverse Events Week 38

    1 Formulieren  
    1. StudyEvent: ODM
      1. Adverse Events Week 38
    ADVERSE EVENTS
    Beschrijving

    ADVERSE EVENTS

    Alias
    UMLS CUI-1
    C0877248 (Adverse event)
    LOINC
    MTHU014542
    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?
    Beschrijving

    Adverse Events

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0877248 (Adverse event)
    LOINC
    MTHU014542
    Terug naar het begin van de pagina

    Similar models

    Adverse Events Week 38

    1 Formulieren
    1. StudyEvent: ODM
      1. Adverse Events Week 38
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    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])
    Terug naar het begin van de pagina 

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