ID

32683

Beskrivning

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

Nyckelord

  1. 2018-11-12 2018-11-12 -
Rättsinnehavare

GSK group of companies

Uppladdad den

12 november 2018

DOI

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Licens

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
Beskrivning

Eligibility Question

Did the subject meet all the entry criteria?
Beskrivning

Did the subject meet all the entry criteria?

Datatyp

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
Beskrivning

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

Datatyp

text

Similar models

Eligibility Question

  1. StudyEvent: ODM
    1. Eligibility Question
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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