ID

32740

Descrizione

Study ID: 107085 Clinical Study ID: GLP107085 Study Title: A Randomized, Double-blind, Parallel, Nested Crossover Study to Investigate the Effect of Albiglutide on Cardiac Repolarization (corrected QT Interval) Compared With Placebo in Healthy Male and Female Subjects: A Thorough ECG Study Employing Placebo, Albiglutide, and a Positive Control (Moxifloxacin) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01406262 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Keywords

  1. 14/11/2018 14/11/2018 -
Titolare del copyright

GSK group of companies

Caricato su

14 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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The Effect of Albiglutide on Cardiac Repolarisation Compared with Placebo 107085

Prior Concomitant Medications and Non-Drug Therapies

Administrative data
Descrizione

Administrative data

Study Name
Descrizione

Study Name

Tipo di dati

text

Site
Descrizione

Site

Tipo di dati

text

Subject
Descrizione

Subject

Tipo di dati

text

Visit Name
Descrizione

Visit Name

Tipo di dati

text

DCI Name/Shortname
Descrizione

DCI Name/Shortname

Tipo di dati

text

Status
Descrizione

Status

Tipo di dati

text

Doc#
Descrizione

Doc#

Tipo di dati

integer

Visit #
Descrizione

Visit #

Tipo di dati

float

Prior Medications and Therapies
Descrizione

Prior Medications and Therapies

Did the subject participate in any Non-Drug Therapies or take Concomitant medications within 30 days prior to screening and/or during the study?
Descrizione

Did the subject participate in any Non-Drug Therapies or take Concomitant medications within 30 days prior to screening and/or during the study?

Tipo di dati

boolean

If Yes, add details on next page (includes over-the counter and prescription drugs) below
Descrizione

If Yes, add details on next page (includes over-the counter and prescription drugs) below

Drug Name
Descrizione

Trade name peferred

Tipo di dati

text

Unit Dose
Descrizione

Unit Dose

Tipo di dati

float

Unit
Descrizione

Unit

Tipo di dati

text

Frequency
Descrizione

Frequency

Tipo di dati

text

Route
Descrizione

Route

Tipo di dati

text

Reason for medication
Descrizione

if SAE/AE enter Event Term

Tipo di dati

text

AE/SAE Event Number
Descrizione

If applicable

Tipo di dati

integer

Start date
Descrizione

Start date

Tipo di dati

date

Stop Date
Descrizione

Stop Date

Tipo di dati

date

Mark if continuing
Descrizione

Mark if continuing

Tipo di dati

text

Taken prior to study
Descrizione

Taken prior to study

Tipo di dati

boolean

Similar models

Prior Concomitant Medications and Non-Drug Therapies

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
Study Name
Item
Study Name
text
Site
Item
Site
text
Subject
Item
Subject
text
Visit Name
Item
Visit Name
text
DCI Name/Shortname
Item
DCI Name/Shortname
text
Status
Item
Status
text
Doc#
Item
Doc#
integer
Visit #
Item
Visit #
float
Item Group
Prior Medications and Therapies
Did the subject participate in any Non-Drug Therapies or take Concomitant medications within 30 days prior to screening and/or during the study?
Item
Did the subject participate in any Non-Drug Therapies or take Concomitant medications within 30 days prior to screening and/or during the study?
boolean
Item Group
If Yes, add details on next page (includes over-the counter and prescription drugs) below
Drug Name
Item
Drug Name
text
Unit Dose
Item
Unit Dose
float
Unit
Item
Unit
text
Frequency
Item
Frequency
text
Route
Item
Route
text
Reason for medication
Item
Reason for medication
text
AE/SAE Event Number
Item
AE/SAE Event Number
integer
Start date
Item
Start date
date
Stop Date
Item
Stop Date
date
Item
Mark if continuing
text
Code List
Mark if continuing
CL Item
Yes (1)
Taken prior to study
Item
Taken prior to study
boolean

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