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ID

32121

Descrição

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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Versões (2)
  1. 19/10/2018 19/10/2018 -
  2. 16/11/2018 16/11/2018 -
Titular dos direitos

GSK group of companies

Transferido a

19 de outubro de 2018

DOI

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Licença

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

    Inglês

    Study Conclusion Form

    1 Formulários  
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Administrative data
    Descrição

    Administrative data

    Subject Identifier
    Descrição

    Subject Identifier

    Tipo de dados

    integer

    Study Conclusion
    Descrição

    Study Conclusion

    Tipo de dados

    text

    Date of subject completion or withdrawal
    Descrição

    Date of subject completion or withdrawal

    Tipo de dados

    date

    Was the subject withdrawn from the study?
    Descrição

    Was the subject withdrawn from the study?

    Tipo de dados

    boolean

    If YES, mark the primary reason for withdrawal:
    Descrição

    If YES, mark the primary reason for withdrawal:

    Tipo de dados

    text

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    Similar models

    Study Conclusion Form

    1 Formulários
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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    Was the subject withdrawn from the study?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    Was the subject withdrawn from the study?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)
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