ID

32567

Beschrijving

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

Trefwoorden

Versies (2)
  1. 06-11-18 06-11-18 -
  2. 07-12-18 07-12-18 -
Houder van rechten

GSK group of companies

Geüploaded op

6 november 2018

DOI

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Licentie

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

Engels

Pharmacokinetics (Liver PK)

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

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

Was a pharmacokinetic blood sample obtained?
Beschrijving

Was a pharmacokinetic blood sample obtained?

Datatype

boolean

If YES, record date sample taken
Beschrijving

If YES, record date sample taken

Datatype

date

If YES, record time sample taken
Beschrijving

If YES, record time sample taken

Datatype

time

Date of last investigational product dose prior to PK sample
Beschrijving

Date of last investigational product dose prior to PK sample

Datatype

date

Time of last investigational product dose prior to PK sample
Beschrijving

Time of last investigational product dose prior to PK sample

Datatype

time

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Similar models

Pharmacokinetics (Liver PK)

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
An unscheduled PK sample must be obtained within 24 hours of last dose
Was a pharmacokinetic blood sample obtained?
Item
Was a pharmacokinetic blood sample obtained?
boolean
If YES, record date sample taken
Item
If YES, record date sample taken
date
If YES, record time sample taken
Item
If YES, record time sample taken
time
Date of last investigational product dose prior to PK sample
Item
Date of last investigational product dose prior to PK sample
date
Time of last investigational product dose prior to PK sample
Item
Time of last investigational product dose prior to PK sample
time
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