ID

32058

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

Mots-clés

  1. 16/10/2018 16/10/2018 -
  2. 30/01/2019 30/01/2019 -
  3. 04/03/2019 04/03/2019 -
Détendeur de droits

GSK group of companies

Téléchargé le

16 octobre 2018

DOI

Pour une demande vous connecter.

Licence

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
Description

Investigational Product

Name of Investigational Product
Description

e.g., Dutasteride

Type de données

text

Date of Dose
Description

Date of Dose

Type de données

date

Time of Dose
Description

Time of Dose

Type de données

time

Treatment Confirmation
Description

Treatment Confirmation

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

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

Type de données

boolean

If NO, record reason(s)
Description

If NO, record reason(s)

Type de données

text

Similar models

Confirmation Form

  1. StudyEvent: ODM
    1. Confirmation Form
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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