ID

23842

Beskrivning

Study part: Exploratory Biomarker Research Week 38 / Early Withdrawal visit.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.

Nyckelord

Versioner (1)
  1. 2017-07-15 2017-07-15 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

15 juli 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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Exploratory Biomarker Research Week 38 Mepolizumab HES NCT00086658

Engelsk

Exploratory Biomarker Research Week 38

1 Formulär  
EXPLORATORY BIOMARKER RESEARCH
Beskrivning

EXPLORATORY BIOMARKER RESEARCH

Alias
UMLS CUI-1
C0005516
Has the subject provided written consent for exploratory biomarker research?
Beskrivning

informed consent biomarker

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0005516
Date of Assessment
Beskrivning

Date of Assessment

Datatyp

date

Alias
UMLS CUI [1]
C2985720
Date of Assessment Skin Biopsy
Beskrivning

Date of Assessment Skin Biopsy

Datatyp

date

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C0150866
Date of Assessment GI Biopsy
Beskrivning

Date of Assessment GI Biopsy

Datatyp

date

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C0005558
UMLS CUI [1,3]
C0017189
Tillbaka till toppen

Similar models

Exploratory Biomarker Research Week 38

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
EXPLORATORY BIOMARKER RESEARCH
C0005516 (UMLS CUI-1)
informed consent biomarker
Item
Has the subject provided written consent for exploratory biomarker research?
boolean
C0021430 (UMLS CUI [1,1])
C0005516 (UMLS CUI [1,2])
Date of Assessment
Item
Date of Assessment
date
C2985720 (UMLS CUI [1])
Date of Assessment Skin Biopsy
Item
Date of Assessment Skin Biopsy
date
C2985720 (UMLS CUI [1,1])
C0150866 (UMLS CUI [1,2])
Date of Assessment GI Biopsy
Item
Date of Assessment GI Biopsy
date
C2985720 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0017189 (UMLS CUI [1,3])
Tillbaka till toppen 

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