ID

33406

Descripción

Study ID: 106837 Clinical Study ID: HZA106837 Study Title: A Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects with Asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01086384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Relvar Study Indication: Asthma

Palabras clave

Versiones (2)
  1. 6/11/18 6/11/18 -
  2. 7/12/18 7/12/18 -
Titular de derechos de autor

GSK group of companies

Subido en

7 de diciembre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Inglés

Pharmacokinetics (Liver PK)

1 formularios  
An unscheduled PK sample must be obtained within 24 hours of last dose
Descripción

An unscheduled PK sample must be obtained within 24 hours of last dose

Alias
UMLS CUI-1
C0201734
UMLS CUI-2
C0370003
Was a pharmacokinetic blood sample obtained?
Descripción

Was a pharmacokinetic blood sample obtained?

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
If YES, record date sample taken
Descripción

If YES, record date sample taken

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0011008
If YES, record time sample taken
Descripción

If YES, record time sample taken

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0201734
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0040223
Date of last investigational product dose prior to PK sample
Descripción

Date of last investigational product dose prior to PK sample

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C1762893
UMLS CUI [2,1]
C0201734
UMLS CUI [2,2]
C0370003
Time of last investigational product dose prior to PK sample
Descripción

Time of last investigational product dose prior to PK sample

Tipo de datos

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0946444
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Similar models

Pharmacokinetics (Liver PK)

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
An unscheduled PK sample must be obtained within 24 hours of last dose
C0201734 (UMLS CUI-1)
C0370003 (UMLS CUI-2)
Was a pharmacokinetic blood sample obtained?
Item
Was a pharmacokinetic blood sample obtained?
boolean
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
If YES, record date sample taken
Item
If YES, record date sample taken
date
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
If YES, record time sample taken
Item
If YES, record time sample taken
time
C0201734 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Date of last investigational product dose prior to PK sample
Item
Date of last investigational product dose prior to PK sample
date
C0304229 (UMLS CUI [1,1])
C1762893 (UMLS CUI [1,2])
C0201734 (UMLS CUI [2,1])
C0370003 (UMLS CUI [2,2])
Time of last investigational product dose prior to PK sample
Item
Time of last investigational product dose prior to PK sample
time
C0304229 (UMLS CUI [1,1])
C0946444 (UMLS CUI [1,2])
Volver a la parte superior de la página 

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