ID

32706

Descrizione

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. 13/11/18 13/11/18 -
Titolare del copyright

GSK group of companies

Caricato su

13 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Estimation of Dose Proportionality of Darapladib - 107038

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

Date of Visit/Assessment
Descrizione

Date of Visit/Assessment

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

Date below is the start of the study for this subject

Tipo di dati

date

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

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

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

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

Tipo di dati

boolean

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

Did the subject experience any adverse events during the study?

Tipo di dati

boolean

Were any repeat ECGs performed?
Descrizione

Were any repeat ECGs performed?

Tipo di dati

boolean

Were any repeat/unscheduled PK samples taken?
Descrizione

Were any repeat/unscheduled PK samples taken?

Tipo di dati

boolean

Were any repeat/unscheduled PD samples taken?
Descrizione

Were any repeat/unscheduled PD samples taken?

Tipo di dati

boolean

Similar models

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial