ID
28330
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)
Keywords
Versions (5)
- 10/11/17 10/11/17 -
- 10/16/17 10/16/17 -
- 10/16/17 10/16/17 -
- 10/23/17 10/23/17 -
- 1/4/18 1/4/18 -
Copyright Holder
GlaxoSmithKline
Uploaded on
January 4, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903
Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903
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.
Description
Start Date Investigational Product
Data type
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0304229
Description
Start Date Investigational Product not applicable
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1272460
Description
End Date Investigational Product
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2361259
Description
End Date Investigational Product not applicable
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2361259
- UMLS CUI [1,3]
- C1272460
Similar models
Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
C2361259 (UMLS CUI [1,2])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
C2361259 (UMLS CUI [1,2])
C2361259 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])