ID

32185

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. 10/23/18 10/23/18 -
  2. 2/25/19 2/25/19 -
Copyright Holder

GSK group of companies

Uploaded on

October 23, 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

Part 2 - Screening Visit - Regimen Form

1 forms  
Administrative data
Description

Administrative data

Subject Identifier
Description

Subject Identifier

Data type

integer

Randomisation Number
Description

Randomisation Number

Record randomisation number
Description

Record randomisation number

Data type

integer

Regimen
Description

Regimen

Complete only for subjects participating in PART 1 of the study.
Description

Record below the treatment assignment for the subject participating in Part 1 of the study Mark one

Data type

text

Complete only for subjects participating in PART 2 of the study
Description

Record below the treatment assignment for the subject participating in Part 2 of the study mark one.

Data type

text

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Similar models

Part 2 - Screening Visit - Regimen Form

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
Randomisation Number
Record randomisation number
Item
Record randomisation number
integer
Item Group
Regimen
Item
Complete only for subjects participating in PART 1 of the study.
text
Record below the treatment assignment for the subject participating in Part 1 of the study.
Code List
Complete only for subjects participating in PART 1 of the study.
CL Item
Part 1 Treatment Sequence 1 ([25])
CL Item
Part 1 Treatment Sequence 2 ([26])
CL Item
Part 1 Treatment Sequence 3 ([27])
CL Item
Part 1 Treatment Sequence 4 ([28])
CL Item
Part 1 Treatment Sequence 5 ([29])
CL Item
Part 1 Treatment Sequence 6 ([30])
Item
Complete only for subjects participating in PART 2 of the study
text
Complete only for subjects participating in PART 2 of the study
Code List
Complete only for subjects participating in PART 2 of the study
CL Item
Treatment D ([20])
CL Item
Treatment E ([21])
CL Item
Treatment F ([22])
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