ID

32706

Description

Study ID: 107038 Clinical Study ID: LPL107038 Study Title: Study to Estimate the Dose Proportionality of the Enteric-Coated Freebase Formulation of SB-480848 Patient Level Data:  Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: Tyrisa ,US Study Indication: Atherosclerosis

Keywords

  1. 11/13/18 11/13/18 -
Copyright Holder

GSK group of companies

Uploaded on

November 13, 2018

DOI

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License

Creative Commons BY-NC 3.0

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Estimation of Dose Proportionality of Darapladib - 107038

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

Date of Visit/Assessment
Description

Date of Visit/Assessment

Date below is the start of the study for this subject
Description

Date below is the start of the study for this subject

Data type

date

Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)
Description

Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)

Were any concomitant medications taken by the subject during the study?
Description

Were any concomitant medications taken by the subject during the study?

Data type

boolean

Did the subject experience any adverse events during the study?
Description

Did the subject experience any adverse events during the study?

Data type

boolean

Were any repeat ECGs performed?
Description

Were any repeat ECGs performed?

Data type

boolean

Were any repeat/unscheduled PK samples taken?
Description

Were any repeat/unscheduled PK samples taken?

Data type

boolean

Were any repeat/unscheduled PD samples taken?
Description

Were any repeat/unscheduled PD samples taken?

Data type

boolean

Similar models

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Date of Visit/Assessment
Date below is the start of the study for this subject
Item
Date below is the start of the study for this subject
date
Item Group
Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)
Were any concomitant medications taken by the subject during the study?
Item
Were any concomitant medications taken by the subject during the study?
boolean
Did the subject experience any adverse events during the study?
Item
Did the subject experience any adverse events during the study?
boolean
Were any repeat ECGs performed?
Item
Were any repeat ECGs performed?
boolean
Were any repeat/unscheduled PK samples taken?
Item
Were any repeat/unscheduled PK samples taken?
boolean
Were any repeat/unscheduled PD samples taken?
Item
Were any repeat/unscheduled PD samples taken?
boolean

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