0 Bedömningar
ID

23752

Beskrivning

Study part: Adverse Events Week 20. 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.

Nyckelord

Versioner (1)
  1. 2017-07-12 2017-07-12 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

12 juli 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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    Adverse Events Week 20 Mepolizumab HES NCT00086658

    Engelsk

    Adverse Events Week 20

    1 Formulär  
    1. StudyEvent: ODM
      1. Adverse Events Week 20
    ADVERSE EVENTS
    Beskrivning

    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?
    Beskrivning

    Adverse Events

    Datatyp

    boolean

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

    Similar models

    Adverse Events Week 20

    1 Formulär
    1. StudyEvent: ODM
      1. Adverse Events Week 20
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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])
    Tillbaka till toppen 

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