ID

32706

Descripción

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

Palabras clave

Versiones (1)
  1. 13/11/18 13/11/18 -
Titular de derechos de autor

GSK group of companies

Subido en

13 de noviembre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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Estimation of Dose Proportionality of Darapladib - 107038

Inglés

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 formularios  
Date of Visit/Assessment
Descripción

Date of Visit/Assessment

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

Date below is the start of the study for this subject

Tipo de datos

date

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

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

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

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

Tipo de datos

boolean

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

Did the subject experience any adverse events during the study?

Tipo de datos

boolean

Were any repeat ECGs performed?
Descripción

Were any repeat ECGs performed?

Tipo de datos

boolean

Were any repeat/unscheduled PK samples taken?
Descripción

Were any repeat/unscheduled PK samples taken?

Tipo de datos

boolean

Were any repeat/unscheduled PD samples taken?
Descripción

Were any repeat/unscheduled PD samples taken?

Tipo de datos

boolean

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Similar models

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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