ID

26349

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: Investigational product (Liver)

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. 04/01/18 04/01/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

16 ottobre 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
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Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

Inglese

Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli  
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Descrizione

If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.

1. Start Date Investigational Product [-99]
Descrizione

Start Date Investigational Product treatment period

Tipo di dati

date

1. Start Date Investigational Product not applicable [-98]
Descrizione

Start Date Investigational Product treatment period not applicable

Tipo di dati

boolean

2. End Date Investigational Product [-99]
Descrizione

End Date Investigational Product treatment period

Tipo di dati

date

2. End Date Investigational Product not applicable [-98]
Descrizione

End Date Investigational Product treatment period not applicable

Tipo di dati

boolean

If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Descrizione

If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.

3. Start Date Investigational Product [-99]
Descrizione

Start Date Investigational Product

Tipo di dati

date

3. Start Date Investigational Product not applicable [-98]
Descrizione

Start Date Investigational Product not applicable

Tipo di dati

boolean

4. End Date Investigational Product [-99]
Descrizione

End Date Investigational Product

Tipo di dati

date

4. End Date Investigational Product not applicable [-98]
Descrizione

End Date Investigational Product not applicable

Tipo di dati

boolean

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Similar models

Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period.
Start Date Investigational Product treatment period
Item
1. Start Date Investigational Product [-99]
date
Start Date Investigational Product treatment period not applicable
Item
1. Start Date Investigational Product not applicable [-98]
boolean
End Date Investigational Product treatment period
Item
2. End Date Investigational Product [-99]
date
End Date Investigational Product treatment period not applicable
Item
2. End Date Investigational Product not applicable [-98]
boolean
Item Group
If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event.
Start Date Investigational Product
Item
3. Start Date Investigational Product [-99]
date
Start Date Investigational Product not applicable
Item
3. Start Date Investigational Product not applicable [-98]
boolean
End Date Investigational Product
Item
4. End Date Investigational Product [-99]
date
End Date Investigational Product not applicable
Item
4. End Date Investigational Product not applicable [-98]
boolean
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