ID

32567

Descrizione

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

Keywords

  1. 06/11/18 06/11/18 -
  2. 07/12/18 07/12/18 -
Titolare del copyright

GSK group of companies

Caricato su

6 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Pharmacokinetics (Liver PK)

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

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

Was a pharmacokinetic blood sample obtained?
Descrizione

Was a pharmacokinetic blood sample obtained?

Tipo di dati

boolean

If YES, record date sample taken
Descrizione

If YES, record date sample taken

Tipo di dati

date

If YES, record time sample taken
Descrizione

If YES, record time sample taken

Tipo di dati

time

Date of last investigational product dose prior to PK sample
Descrizione

Date of last investigational product dose prior to PK sample

Tipo di dati

date

Time of last investigational product dose prior to PK sample
Descrizione

Time of last investigational product dose prior to PK sample

Tipo di dati

time

Similar models

Pharmacokinetics (Liver PK)

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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