ID

32683

Descrizione

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. 12/11/18 12/11/18 -
Titolare del copyright

GSK group of companies

Caricato su

12 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

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
Descrizione

Eligibility Question

Did the subject meet all the entry criteria?
Descrizione

Did the subject meet all the entry criteria?

Tipo di dati

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
Descrizione

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

Tipo di dati

text

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Eligibility Question

  1. StudyEvent: ODM
    1. Eligibility Question
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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