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ID

32683

Description

Study ID: 107038 Clinical Study ID: LPL107038 Study Title: Study to Estimate the Dose Proportionality of the Enteric-Coated Freebase Formulation of SB-480848 Patient Level Data:  Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: Tyrisa ,US Study Indication: Atherosclerosis

Keywords

  1. 11/12/18 11/12/18 -
Copyright Holder

GSK group of companies

Uploaded on

November 12, 2018

DOI

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License

Creative Commons BY-NC 3.0

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    Estimation of Dose Proportionality of Darapladib - 107038

    Eligibility Question

    1. StudyEvent: ODM
      1. Eligibility Question
    Eligibility Question
    Description

    Eligibility Question

    Did the subject meet all the entry criteria?
    Description

    Did the subject meet all the entry criteria?

    Data type

    boolean

    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    Description

    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below

    Data type

    text

    Similar models

    Eligibility Question

    1. StudyEvent: ODM
      1. Eligibility Question
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Eligibility Question
    Did the subject meet all the entry criteria?
    Item
    Did the subject meet all the entry criteria?
    boolean
    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    Item
    Do not admit he subject into this study if any Inclusion/Exclusion criteria is violated unless an exception has been granted by the GSK Medical Monitor and subject is continuing in the study. Please clarify the exemption(s) below
    text

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