ID

32058

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

  1. 16/10/2018 16/10/2018 -
  2. 30/01/2019 30/01/2019 -
  3. 04/03/2019 04/03/2019 -
Titular dos direitos

GSK group of companies

Transferido a

16 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

Confirmation Form

  1. StudyEvent: ODM
    1. Confirmation Form
Investigational Product
Descrição

Investigational Product

Name of Investigational Product
Descrição

e.g., Dutasteride

Tipo de dados

text

Date of Dose
Descrição

Date of Dose

Tipo de dados

date

Time of Dose
Descrição

Time of Dose

Tipo de dados

time

Treatment Confirmation
Descrição

Treatment Confirmation

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Descrição

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?

Tipo de dados

boolean

If NO, record reason(s)
Descrição

If NO, record reason(s)

Tipo de dados

text

Similar models

Confirmation Form

  1. StudyEvent: ODM
    1. Confirmation Form
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Investigational Product
Name of Investigational Product
Item
Name of Investigational Product
text
Date of Dose
Item
Date of Dose
date
Time of Dose
Item
Time of Dose
time
Item Group
Treatment Confirmation
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
boolean
If NO, record reason(s)
Item
If NO, record reason(s)
text

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