ID

32706

Beschreibung

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

Stichworte

Versionen (1)
  1. 13.11.18 13.11.18 -
Rechteinhaber

GSK group of companies

Hochgeladen am

13. November 2018

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY-NC 3.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Estimation of Dose Proportionality of Darapladib - 107038

Englisch

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 Formulare  
Date of Visit/Assessment
Beschreibung

Date of Visit/Assessment

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

Date below is the start of the study for this subject

Datentyp

date

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

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

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

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

Datentyp

boolean

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

Did the subject experience any adverse events during the study?

Datentyp

boolean

Were any repeat ECGs performed?
Beschreibung

Were any repeat ECGs performed?

Datentyp

boolean

Were any repeat/unscheduled PK samples taken?
Beschreibung

Were any repeat/unscheduled PK samples taken?

Datentyp

boolean

Were any repeat/unscheduled PD samples taken?
Beschreibung

Were any repeat/unscheduled PD samples taken?

Datentyp

boolean

Zum Seitenanfang zurückkehren

Ähnliche Modelle

Logs and Repeats: General Adverse Event and Concomitant Medication Questions

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video