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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

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Versions (1)
  1. 12/11/2018 12/11/2018 -
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GSK group of companies

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12 novembre 2018

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Creative Commons BY-NC 3.0
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    Estimation of Dose Proportionality of Darapladib - 107038

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    Eligibility Question

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    1. StudyEvent: ODM
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    Eligibility Question
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    Did the subject meet all the entry criteria?
    Description

    Did the subject meet all the entry criteria?

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    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
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    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

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    Eligibility Question

    1 Formulaires
    1. StudyEvent: ODM
      1. Eligibility Question
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    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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