ID

32117

Description

Study ID: 106218 Clinical Study ID: TDC106218 Study Title: Study On Bioavailability And Pharmacokinetics Of Various Doses Of Testosterone Administered With And Without Dutasteride  Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: testosterone Trade Name: Andropatch,Androderm Study Indication: Hypogonadism, Male

Keywords

Versions (2)
  1. 10/19/18 10/19/18 -
  2. 12/18/18 12/18/18 -
Copyright Holder

GSK group of companies

Uploaded on

October 19, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

English

Pharmacogenetic Research Results (PGx)

1 forms  
Administrative data
Description

Administrative data

Subject Identifier
Description

Subject Identifier

Data type

integer

PGx-Pharmacogenetic Research
Description

PGx-Pharmacogenetic Research

Consent for PGx-Pharmacogenetic Research (DNA)
Description

Consent for PGx-Pharmacogenetic Research (DNA)

Data type

text

Has informed consent been obtained for PGx-Pharmacigenetic research?
Description

Has informed consent been obtained for PGx-Pharmacigenetic research?

Data type

boolean

If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
Description

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

Data type

date

If NO, mark one reason:
Description

If NO, mark one reason:

Data type

text

Blood Sample Collection (DNA)
Description

Blood Sample Collection (DNA)

Has a blood sample been collected for PGx-Pharmacocinetic research?
Description

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

Data type

boolean

If YES, record the date sample taken
Description

If YES, record the date sample taken

Data type

date

Withdrawal of Consent
Description

Withdrawal of Consent

Has subject withdrawn consent for PGx-Pharmacogenetic research?
Description

Has subject withdrawn consent for PGx-Pharmacogenetic research?

Data type

boolean

Blood Sample Destruction
Description

Blood Sample Destruction

Has a request been made for blood sample destruction?
Description

Has a request been made for blood sample destruction?

Data type

boolean

If YES, mark one reason:
Description

If YES, mark one reason:

Data type

text

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Similar models

Pharmacogenetic Research Results (PGx)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
PGx-Pharmacogenetic Research
Consent for PGx-Pharmacogenetic Research (DNA)
Item
Consent for PGx-Pharmacogenetic Research (DNA)
text
Has informed consent been obtained for PGx-Pharmacigenetic research?
Item
Has informed consent been obtained for PGx-Pharmacigenetic research?
boolean
If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
Item
If YES, record the date informed consent obtained for PGx-Pharmacogenetic research
date
Item
If NO, mark one reason:
text
If NO, mark one reason:
Code List
If NO, mark one reason:
CL Item
[1] Subject declined (1)
CL Item
[2] Subject not asked by Investigator (2)
CL Item
[Z] Other, specify__________________________ (3)
Item Group
Blood Sample Collection (DNA)
Has a blood sample been collected for PGx-Pharmacocinetic research?
Item
Has a blood sample been collected for PGx-Pharmacocinetic research?
boolean
If YES, record the date sample taken
Item
If YES, record the date sample taken
date
Item Group
Withdrawal of Consent
Has subject withdrawn consent for PGx-Pharmacogenetic research?
Item
Has subject withdrawn consent for PGx-Pharmacogenetic research?
boolean
Item Group
Blood Sample Destruction
Has a request been made for blood sample destruction?
Item
Has a request been made for blood sample destruction?
boolean
Item
If YES, mark one reason:
text
If YES, mark one reason:
Code List
If YES, mark one reason:
CL Item
[1] Subject requested (1)
CL Item
[2] Screen failure (2)
CL Item
[Z] Other, specify________________________ (3)
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