ID

26198

Description

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)

Mots-clés

Versions (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 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

11 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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

Anglais

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

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

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]
Description

Start Date Investigational Product treatment period

Type de données

date

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

Start Date Investigational Product treatment period not applicable

Type de données

boolean

2. End Date Investigational Product [-99]
Description

End Date Investigational Product treatment period

Type de données

date

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

End Date Investigational Product treatment period not applicable

Type de données

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.
Description

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]
Description

Start Date Investigational Product

Type de données

date

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

Start Date Investigational Product not applicable

Type de données

boolean

4. End Date Investigational Product [-99]
Description

End Date Investigational Product

Type de données

date

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

End Date Investigational Product not applicable

Type de données

boolean

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Similar models

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

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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