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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

Palavras-chave

19/10/2018 19/10/2018 -
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

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Detalhes

Study Conclusion Form

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Was the subject withdrawn from the study?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Was the subject withdrawn from the study?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

Yes

No

If YES, mark the primary reason for withdrawal:

Descrição

If YES, mark the primary reason for withdrawal:

Tipo de dados

text

[1] Adverse event -> Record details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate. (1)

[2] Lost to follow-up (2)

[3] Protocol violation (3)

[4] Subject decided to withdraw from the study (4)

[6] Sponsor terminated study (5)

[Z] Other, specify______________________________ (6)

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Study Conclusion Form

StudyEvent: ODM
1. Study Conclusion Form

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Administrative data

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Was the subject withdrawn from the study?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Was the subject withdrawn from the study?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

If YES, mark the primary reason for withdrawal:

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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