ID

23612

Beschrijving

Study part: Investigational Product – IV Dosing Week 8. A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Trefwoorden

Versies (1)
  1. 09-07-17 09-07-17 -
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GlaxoSmithKline

Geüploaded op

9 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Investigational Product – IV Dosing Week 8 Mepolizumab HES NCT00086658

Engels

Investigational Product – IV Dosing Week 8

1 Formulieren  
INVESTIGATIONAL PRODUCT - IV DOSING
Beschrijving

INVESTIGATIONAL PRODUCT - IV DOSING

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0678766
UMLS CUI-3
C0348016
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Infusion Start Date
Beschrijving

Infusion Start Date

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0574032
UMLS CUI [1,3]
C0439659
Infusion Start Time
Beschrijving

Infusion Start Time

Datatype

time

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C0439659
UMLS CUI [1,3]
C0040223
Infusion Stop Date
Beschrijving

Stop Date Infusion

Datatype

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0574032
Infusion Stop Time
Beschrijving

Stop Time Infusion

Datatype

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0574032
Dose
Beschrijving

Dose

Datatype

integer

Alias
UMLS CUI [1]
C3174092
Units
Beschrijving

Units

Datatype

text

Alias
UMLS CUI [1]
C1519795
Terug naar het begin van de pagina

Similar models

Investigational Product – IV Dosing Week 8

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
INVESTIGATIONAL PRODUCT - IV DOSING
C0304229 (UMLS CUI-1)
C0678766 (UMLS CUI-2)
C0348016 (UMLS CUI-3)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Infusion Start Date
Item
Infusion Start Date
date
C0011008 (UMLS CUI [1,1])
C0574032 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
Infusion Start Time
Item
Infusion Start Time
time
C0574032 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Stop Date Infusion
Item
Infusion Stop Date
date
C0806020 (UMLS CUI [1,1])
C0574032 (UMLS CUI [1,2])
Stop Time Infusion
Item
Infusion Stop Time
time
C1522314 (UMLS CUI [1,1])
C0574032 (UMLS CUI [1,2])
Dose
Item
Dose
integer
C3174092 (UMLS CUI [1])
Units
Item
Units
text
C1519795 (UMLS CUI [1])
Terug naar het begin van de pagina 

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