ID

32713

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. 13/11/18 13/11/18 -
Titular de derechos de autor

GSK group of companies

Subido en

13 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

PGx-Pharmacogenetic Research Consent

1 formularios  
PGx-Pharmacogenetic Research Consent Question
Descripción

PGx-Pharmacogenetic Research Consent Question

Has Informed consent been obtained for PGx-Pharmacogenetic research?
Descripción

Has Informed consent been obtained for PGx-Pharmacogenetic research?

Tipo de datos

boolean

If YES, record Date informed consent obtained for PGx-Pharmacogenetic research
Descripción

If YES, record Date informed consent obtained for PGx-Pharmacogenetic research

Tipo de datos

date

If NO, check reason
Descripción

If NO, check reason

Tipo de datos

text

If OTHER, specify
Descripción

If OTHER, specify

Tipo de datos

text

Has a blood sample been collected for PGx-pharmacogenetic research?
Descripción

Has a blood sample been collected for PGx-pharmacogenetic research?

Tipo de datos

boolean

If YES, record date sample taken
Descripción

If YES, record date sample taken

Tipo de datos

boolean

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Similar models

PGx-Pharmacogenetic Research Consent

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
PGx-Pharmacogenetic Research Consent Question
Has Informed consent been obtained for PGx-Pharmacogenetic research?
Item
Has Informed consent been obtained for PGx-Pharmacogenetic research?
boolean
If YES, record Date informed consent obtained for PGx-Pharmacogenetic research
Item
If YES, record Date informed consent obtained for PGx-Pharmacogenetic research
date
Item
If NO, check reason
text
If NO, check reason
Code List
If NO, check reason
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other (3)
If OTHER, specify
Item
If OTHER, specify
text
Has a blood sample been collected for PGx-pharmacogenetic research?
Item
Has a blood sample been collected for PGx-pharmacogenetic research?
boolean
If YES, record date sample taken
Item
If YES, record date sample taken
boolean
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