ID

28330

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

4 de janeiro de 2018

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

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
1. Start Date Investigational Product not applicable [-98]
Descrição

Start Date Investigational Product treatment period not applicable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
2. End Date Investigational Product [-99]
Descrição

End Date Investigational Product treatment period

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
2. End Date Investigational Product not applicable [-98]
Descrição

End Date Investigational Product treatment period not applicable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460
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

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
3. Start Date Investigational Product not applicable [-98]
Descrição

Start Date Investigational Product not applicable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1272460
4. End Date Investigational Product [-99]
Descrição

End Date Investigational Product

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
4. End Date Investigational Product not applicable [-98]
Descrição

End Date Investigational Product not applicable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2361259
UMLS CUI [1,3]
C1272460
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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
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product treatment period not applicable
Item
1. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product treatment period
Item
2. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product treatment period not applicable
Item
2. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
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
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date Investigational Product not applicable
Item
3. Start Date Investigational Product not applicable [-98]
boolean
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
End Date Investigational Product
Item
4. End Date Investigational Product [-99]
date
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
End Date Investigational Product not applicable
Item
4. End Date Investigational Product not applicable [-98]
boolean
C0304229 (UMLS CUI [1,1])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
Voltar ao início da página 

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