ID
28319
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: Other endpoints - Repeating form (Scheduled visits)
Trefwoorden
Versies (3)
- 09-10-17 09-10-17 -
- 23-10-17 23-10-17 -
- 03-01-18 03-01-18 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
3 januari 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Other endpoints GSK study Chronic Coronary Heart Disease NCT00799903
Other endpoints GSK study Chronic Coronary Heart Disease NCT00799903
Beschrijving
CEC Status
Beschrijving
[hidden] Item is not required
Datatype
text
Alias
- UMLS CUI [1]
- C2826275
Beschrijving
Use SAE Sequence number from the corresponding SAE form (the last item on the form, in the "Non-Clinical" section) [hidden]. Item is not required.
Datatype
text
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
Copy Serious Adverse Event term from corresponding SAE form [hidden]. Item is not required.
Datatype
text
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C2826934
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