ID

23750

Descrizione

Study part: Concomitant Medications 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.

Keywords

  1. 12/07/17 12/07/17 -
Titolare del copyright

GlaxoSmithKline

Caricato su

12 luglio 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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    Concomitant Medications Week 20 Mepolizumab HES NCT00086658

    Concomitant Medications Week 20

    CONCOMITANT MEDICATIONS
    Descrizione

    CONCOMITANT MEDICATIONS

    Alias
    UMLS CUI-1
    C2347852 (Concomitant Agent)
    Are changes to the subject’s concomitant medications or any new medications taken since the last visit in the appropriate Concomitant Medications recorded?
    Descrizione

    Concomitant Medications

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C2347852 (Concomitant Agent)

    Similar models

    Concomitant Medications Week 20

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    CONCOMITANT MEDICATIONS
    C2347852 (UMLS CUI-1)
    Concomitant Medications
    Item
    Are changes to the subject’s concomitant medications or any new medications taken since the last visit in the appropriate Concomitant Medications recorded?
    boolean
    C2347852 (UMLS CUI [1])

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