ID
28330
Beschrijving
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)
Trefwoorden
Versies (5)
- 11-10-17 11-10-17 -
- 16-10-17 16-10-17 -
- 16-10-17 16-10-17 -
- 23-10-17 23-10-17 -
- 04-01-18 04-01-18 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
4 januari 2018
DOI
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Licentie
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
Beschrijving
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.
Beschrijving
Start Date Investigational Product
Datatype
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0304229
Beschrijving
Start Date Investigational Product not applicable
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1272460
Beschrijving
End Date Investigational Product
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2361259
Beschrijving
End Date Investigational Product not applicable
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2361259
- UMLS CUI [1,3]
- C1272460
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Investigational product (Liver) GSK study Chronic Coronary Heart Disease NCT00799903
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C0304229 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
C2361259 (UMLS CUI [1,2])
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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])