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ID

23842

Description

Study part: Exploratory Biomarker Research 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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Versions (1)
  1. 15/07/2017 15/07/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

15 juillet 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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    Exploratory Biomarker Research Week 38 Mepolizumab HES NCT00086658

    Anglais

    Exploratory Biomarker Research Week 38

    1 Formulaires  
    EXPLORATORY BIOMARKER RESEARCH
    Description

    EXPLORATORY BIOMARKER RESEARCH

    Alias
    UMLS CUI-1
    C0005516
    Has the subject provided written consent for exploratory biomarker research?
    Description

    informed consent biomarker

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0005516
    Date of Assessment
    Description

    Date of Assessment

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2985720
    Date of Assessment Skin Biopsy
    Description

    Date of Assessment Skin Biopsy

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C0150866
    Date of Assessment GI Biopsy
    Description

    Date of Assessment GI Biopsy

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C0005558
    UMLS CUI [1,3]
    C0017189
    Retour au début de la page

    Similar models

    Exploratory Biomarker Research Week 38

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    EXPLORATORY BIOMARKER RESEARCH
    C0005516 (UMLS CUI-1)
    informed consent biomarker
    Item
    Has the subject provided written consent for exploratory biomarker research?
    boolean
    C0021430 (UMLS CUI [1,1])
    C0005516 (UMLS CUI [1,2])
    Date of Assessment
    Item
    Date of Assessment
    date
    C2985720 (UMLS CUI [1])
    Date of Assessment Skin Biopsy
    Item
    Date of Assessment Skin Biopsy
    date
    C2985720 (UMLS CUI [1,1])
    C0150866 (UMLS CUI [1,2])
    Date of Assessment GI Biopsy
    Item
    Date of Assessment GI Biopsy
    date
    C2985720 (UMLS CUI [1,1])
    C0005558 (UMLS CUI [1,2])
    C0017189 (UMLS CUI [1,3])
    Retour au début de la page 

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