0 Bedömningar
ID

22717

Beskrivning

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.

Nyckelord

Versioner (1)
  1. 2017-06-11 2017-06-11 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

11 juni 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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    Adverse Events Screening Visit Mepolizumab HES NCT00086658

    Engelsk

    Adverse Events Screening Visit

    1 Formulär  
    ADVERSE EVENTS
    Beskrivning

    ADVERSE EVENTS

    Alias
    UMLS CUI-1
    C0877248
    AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?
    Beskrivning

    Adverse Events

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0877248
    Tillbaka till toppen

    Similar models

    Adverse Events Screening Visit

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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])
    Tillbaka till toppen 

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