ID

32683

Descripción

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

Palabras clave

Versiones (1)
  1. 12/11/18 12/11/18 -
Titular de derechos de autor

GSK group of companies

Subido en

12 de noviembre de 2018

DOI

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Licencia

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

Inglés

Eligibility Question

1 formularios  
  1. StudyEvent: ODM
    1. Eligibility Question
Eligibility Question
Descripción

Eligibility Question

Did the subject meet all the entry criteria?
Descripción

Did the subject meet all the entry criteria?

Tipo de datos

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
Descripción

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 de datos

text

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Eligibility Question

1 formularios
  1. StudyEvent: ODM
    1. Eligibility Question
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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