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

Mots-clés

Versions (1)
  1. 13/11/2018 13/11/2018 -
Détendeur de droits

GSK group of companies

Téléchargé le

13 novembre 2018

DOI

Pour une demande vous connecter.

Licence

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

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Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 Formulaires  
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

Type de données

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?

Type de données

boolean

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

Did the subject experience any adverse events during the study?

Type de données

boolean

Were any repeat ECGs performed?
Description

Were any repeat ECGs performed?

Type de données

boolean

Were any repeat/unscheduled PK samples taken?
Description

Were any repeat/unscheduled PK samples taken?

Type de données

boolean

Were any repeat/unscheduled PD samples taken?
Description

Were any repeat/unscheduled PD samples taken?

Type de données

boolean

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Similar models

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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
Retour au début de la page 

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