ID

38719

Descripción

Study ID: 109035 Clinical Study ID: 109035 Study Title: A Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of GSK163090 in Subjects With Major Depressive Disorder Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00896363 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK163090 1 mg, GSK163090 Placebo, GSK163090 3 mg Trade Name: Study Indication: Depressive Disorder

Palabras clave

Versiones (1)
  1. 30/10/19 30/10/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

30 de octubre de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

Inglés

Pharmacokinetics Blood

1 formularios  
  1. StudyEvent: ODM
    1. Pharmacokinetics Blood
Dosing Date and Time
Descripción

Dosing Date and Time

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
UMLS CUI-3
C0011008
UMLS CUI-4
C0040223
Dosing date/time
Descripción

Experimental drug, Dosage, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Pre AM Dose
Descripción

Pre AM Dose

Alias
UMLS CUI-1
C0031328
UMLS CUI-2
C0439565
UMLS CUI-3
C0332170
Actual date/time
Descripción

Pharmacokinetics aspects, Pre-dose, Morning, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0439565
UMLS CUI [1,3]
C0332170
UMLS CUI [1,4]
C0011008
UMLS CUI [1,5]
C0040223
Sample identifier
Descripción

Pharmacokinetics aspects, Pre-dose, Morning, Sample identification number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0439565
UMLS CUI [1,3]
C0332170
UMLS CUI [1,4]
C1299222
4-6 H Post AM Dose
Descripción

4-6 H Post AM Dose

Alias
UMLS CUI-1
C0031328
UMLS CUI-2
C0439568
UMLS CUI-3
C0332170
Actual date/time
Descripción

Pharmacokinetics aspects, Post-dose, Morning, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0439568
UMLS CUI [1,3]
C0332170
UMLS CUI [1,4]
C0011008
UMLS CUI [1,5]
C0040223
Sample identifier
Descripción

Pharmacokinetics aspects, Post-dose, Morning, Sample identification number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0439568
UMLS CUI [1,3]
C0332170
UMLS CUI [1,4]
C1299222
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Similar models

Pharmacokinetics Blood

1 formularios
  1. StudyEvent: ODM
    1. Pharmacokinetics Blood
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Dosing Date and Time
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C0011008 (UMLS CUI-3)
C0040223 (UMLS CUI-4)
Experimental drug, Dosage, Date in time, Time
Item
Dosing date/time
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item Group
Pre AM Dose
C0031328 (UMLS CUI-1)
C0439565 (UMLS CUI-2)
C0332170 (UMLS CUI-3)
Pharmacokinetics aspects, Pre-dose, Morning, Date in time, Time
Item
Actual date/time
datetime
C0031328 (UMLS CUI [1,1])
C0439565 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Pharmacokinetics aspects, Pre-dose, Morning, Sample identification number
Item
Sample identifier
integer
C0031328 (UMLS CUI [1,1])
C0439565 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C1299222 (UMLS CUI [1,4])
Item Group
4-6 H Post AM Dose
C0031328 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
C0332170 (UMLS CUI-3)
Pharmacokinetics aspects, Post-dose, Morning, Date in time, Time
Item
Actual date/time
datetime
C0031328 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Pharmacokinetics aspects, Post-dose, Morning, Sample identification number
Item
Sample identifier
integer
C0031328 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C1299222 (UMLS CUI [1,4])
Volver a la parte superior de la página 

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