ID

22769

Description

Study part: Randomisation Number Day 1 Post- Infection. 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.

Keywords

Versions (1)
  1. 6/11/17 6/11/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 11, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Randomisation Number Day 1 Post- Infection Mepolizumab HES NCT00086658

English

Randomisation Number Day 1 Post- Infection

1 forms  
RANDOMISATION NUMBER
Description

RANDOMISATION NUMBER

Alias
UMLS CUI-1
C0034656
UMLS CUI-2
C0237753
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Record randomisation number.
Description

Randomisation Number

Data type

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Date of randomisation
Description

date randomisation

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0034656
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Similar models

Randomisation Number Day 1 Post- Infection

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
RANDOMISATION NUMBER
C0034656 (UMLS CUI-1)
C0237753 (UMLS CUI-2)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Randomisation Number
Item
Record randomisation number.
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
date randomisation
Item
Date of randomisation
date
C0011008 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
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