ID

26202

Descrizione

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Pharmacokinetics (Liver PK)

Keywords

versioni (5)
  1. 11/10/17 11/10/17 -
  2. 16/10/17 16/10/17 -
  3. 16/10/17 16/10/17 -
  4. 23/10/17 23/10/17 -
  5. 11/01/18 11/01/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

11 ottobre 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
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Pharmacokinetics Liver GSK study Chronic Coronary Heart Disease NCT00799903

Inglese

Pharmacokinetics Liver GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli  
An unscheduled PK blood sample must be obtained within 72 hours of last dose.
Descrizione

An unscheduled PK blood sample must be obtained within 72 hours of last dose.

1. Was a pharmacokinetic blood sample obtained?
Descrizione

pharmacokinetic blood sample

Tipo di dati

boolean

If yes, date sample taken
Descrizione

date blood sample taken

Tipo di dati

date

If yes, time sample taken
Descrizione

time blood sample taken

Tipo di dati

time

If Yes, date of last investigational product dose prior to PK sample
Descrizione

date last investigational product dose prior to PK sample

Tipo di dati

date

If Yes, time of last investigational product dose prior to PK sample
Descrizione

time last investigational product dose prior to PK sample

Tipo di dati

time

Sample Identifier/Sample Number
Descrizione

Sample Identifier and Sample Number are conditional. The study team must choose one for inclusion on the eCRF form.

Tipo di dati

text

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Similar models

Pharmacokinetics Liver GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
An unscheduled PK blood sample must be obtained within 72 hours of last dose.
pharmacokinetic blood sample
Item
1. Was a pharmacokinetic blood sample obtained?
boolean
date blood sample taken
Item
If yes, date sample taken
date
time blood sample taken
Item
If yes, time sample taken
time
date last investigational product dose prior to PK sample
Item
If Yes, date of last investigational product dose prior to PK sample
date
time last investigational product dose prior to PK sample
Item
If Yes, time of last investigational product dose prior to PK sample
time
Sample Identifier/Sample Number
Item
Sample Identifier/Sample Number
text
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