ID

30894

Description

Study part: PGx- Pharmacogenetic. A phase 1 single-masked, randomized (with respect to placebo), placebo-controlled, parallel-group, dose-rising study to evaluate the safety, tolerability and pharmacokinetics of repeat oral doses of GW786034 in elderly healthy volunteers. Trade Name: Votrient. Clinical Study ID: MD1103367.

Keywords

  1. 7/2/18 7/2/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 2, 2018

DOI

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License

Creative Commons BY-NC 3.0

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PGx- Pharmacogenetic Pazopanib Macular Degeneration MD1103367

PGx- Pharmacogenetic

  1. StudyEvent: ODM
    1. PGx- Pharmacogenetic
PGx-PHARMACOGENETIC RESEARCH CONSENT (PGx Consent)
Description

PGx-PHARMACOGENETIC RESEARCH CONSENT (PGx Consent)

Alias
UMLS CUI-1
C0031325
UMLS CUI-3
C1511481
Has informed consent been obtained for PGx-Pharmacogenetic research?
Description

informed consent; Pharmacogenetic

Data type

text

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0031325
When informed consent been obtained, date informed consent obtained for PGx-Pharmacogenetic research
Description

date informed consent; Pharmacogenetic

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0021430
UMLS CUI [2]
C0031325
Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
Description

blood sample

Data type

text

Alias
UMLS CUI [1]
C0005834
Yes, record date sample taken
Description

date sample taken

Data type

date

Alias
UMLS CUI [1]
C1302413
No, check reason
Description

reason

Data type

text

Alias
UMLS CUI [1]
C0566251
Other, specify
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394
PGx-PHARMACOGENETIC RESEARCH WITHDRAWAL OF CONSENT (PGx Withdraw)
Description

PGx-PHARMACOGENETIC RESEARCH WITHDRAWAL OF CONSENT (PGx Withdraw)

Alias
UMLS CUI-1
C1707492
Has subject withdrawn consent for PGx-Pharmacogenetic research?
Description

Consent Withdrawn

Data type

text

Alias
UMLS CUI [1]
C1707492
Has a request been made for sample destruction?
Description

sample destruction

Data type

text

Alias
UMLS CUI [1,1]
C0370003
UMLS CUI [1,2]
C1948029
When yes
Description

reason

Data type

text

Alias
UMLS CUI [1]
C0566251
Other, specify
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394

Similar models

PGx- Pharmacogenetic

  1. StudyEvent: ODM
    1. PGx- Pharmacogenetic
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
PGx-PHARMACOGENETIC RESEARCH CONSENT (PGx Consent)
C0031325 (UMLS CUI-1)
C1511481 (UMLS CUI-3)
Item
Has informed consent been obtained for PGx-Pharmacogenetic research?
text
C0021430 (UMLS CUI [1])
C0031325 (UMLS CUI [2])
Code List
Has informed consent been obtained for PGx-Pharmacogenetic research?
CL Item
Yes (Y)
CL Item
No (N)
date informed consent; Pharmacogenetic
Item
When informed consent been obtained, date informed consent obtained for PGx-Pharmacogenetic research
date
C0011008 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0031325 (UMLS CUI [2])
Item
Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
text
C0005834 (UMLS CUI [1])
Code List
Has a blood sample been collected for PGx-pharmacogenetic (DNA) research?
CL Item
Yes (Y)
CL Item
No (N)
date sample taken
Item
Yes, record date sample taken
date
C1302413 (UMLS CUI [1])
Item
No, check reason
text
C0566251 (UMLS CUI [1])
Code List
No, check reason
CL Item
Subject declined  (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other (Z)
Other
Item
Other, specify
text
C0205394 (UMLS CUI [1])
Item Group
PGx-PHARMACOGENETIC RESEARCH WITHDRAWAL OF CONSENT (PGx Withdraw)
C1707492 (UMLS CUI-1)
Item
Has subject withdrawn consent for PGx-Pharmacogenetic research?
text
C1707492 (UMLS CUI [1])
Code List
Has subject withdrawn consent for PGx-Pharmacogenetic research?
CL Item
Yes (Y)
CL Item
No (N)
Item
Has a request been made for sample destruction?
text
C0370003 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
Code List
Has a request been made for sample destruction?
CL Item
Yes (Y)
CL Item
No (N)
Item
When yes
text
C0566251 (UMLS CUI [1])
Code List
When yes
CL Item
Subject requested  (1)
CL Item
Screen failure  (2)
CL Item
Other (Z)
Other
Item
Other, specify
text
C0205394 (UMLS CUI [1])

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