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ID

32121

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

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Versions (2)
  1. 10/19/18 10/19/18 -
  2. 11/16/18 11/16/18 -
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

    Study Conclusion Form

    1 forms  
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Administrative data
    Description

    Administrative data

    Subject Identifier
    Description

    Subject Identifier

    Data type

    integer

    Study Conclusion
    Description

    Study Conclusion

    Data type

    text

    Date of subject completion or withdrawal
    Description

    Date of subject completion or withdrawal

    Data type

    date

    Was the subject withdrawn from the study?
    Description

    Was the subject withdrawn from the study?

    Data type

    boolean

    If YES, mark the primary reason for withdrawal:
    Description

    If YES, mark the primary reason for withdrawal:

    Data type

    text

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    Similar models

    Study Conclusion Form

    1 forms
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative data
    Subject Identifier
    Item
    Subject Identifier
    integer
    Study Conclusion
    Item
    Study Conclusion
    text
    Date of subject completion or withdrawal
    Item
    Date of subject completion or withdrawal
    date
    Was the subject withdrawn from the study?
    Item
    Was the subject withdrawn from the study?
    boolean
    Item
    If YES, mark the primary reason for withdrawal:
    text
    If YES, mark the primary reason for withdrawal:
    Code List
    If YES, mark the primary reason for withdrawal:
    CL Item
    [1] Adverse event -> Record details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate. (1)
    CL Item
    [2] Lost to follow-up (2)
    CL Item
    [3] Protocol violation (3)
    CL Item
    [4] Subject decided to withdraw from the study (4)
    CL Item
    [6] Sponsor terminated study (5)
    CL Item
    [Z] Other, specify______________________________ (6)
    Back to the top of the page 

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