ID

32567

Descrição

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

Palavras-chave

  1. 06/11/2018 06/11/2018 -
  2. 07/12/2018 07/12/2018 -
Titular dos direitos

GSK group of companies

Transferido a

6 de novembro de 2018

DOI

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Licença

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
Descrição

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

Was a pharmacokinetic blood sample obtained?
Descrição

Was a pharmacokinetic blood sample obtained?

Tipo de dados

boolean

If YES, record date sample taken
Descrição

If YES, record date sample taken

Tipo de dados

date

If YES, record time sample taken
Descrição

If YES, record time sample taken

Tipo de dados

time

Date of last investigational product dose prior to PK sample
Descrição

Date of last investigational product dose prior to PK sample

Tipo de dados

date

Time of last investigational product dose prior to PK sample
Descrição

Time of last investigational product dose prior to PK sample

Tipo de dados

time

Similar models

Pharmacokinetics (Liver PK)

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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