ID

26355

Descrição

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)

Palavras-chave

Versões (5)
  1. 11/10/2017 11/10/2017 -
  2. 16/10/2017 16/10/2017 -
  3. 16/10/2017 16/10/2017 -
  4. 23/10/2017 23/10/2017 -
  5. 04/01/2018 04/01/2018 -
Titular dos direitos

GlaxoSmithKline

Transferido a

16 de outubro de 2017

DOI

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Licença

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

Inglês

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

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

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]
Descrição

Start Date Investigational Product treatment period

Tipo de dados

date

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

Start Date Investigational Product treatment period not applicable

Tipo de dados

boolean

2. End Date Investigational Product [-99]
Descrição

End Date Investigational Product treatment period

Tipo de dados

date

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

End Date Investigational Product treatment period not applicable

Tipo de dados

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.
Descrição

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]
Descrição

Start Date Investigational Product

Tipo de dados

date

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

Start Date Investigational Product not applicable

Tipo de dados

boolean

4. End Date Investigational Product [-99]
Descrição

End Date Investigational Product

Tipo de dados

date

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

End Date Investigational Product not applicable

Tipo de dados

boolean

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Similar models

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

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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
Voltar ao início da página 

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