ID

23765

Description

Study part: Exploratory Biomarker Research Week 24.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.

Mots-clés

  1. 12/07/2017 12/07/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

12 juillet 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Exploratory Biomarker Research Week 24 Mepolizumab HES NCT00086658

Exploratory Biomarker Research Week 24

EXPLORATORY BIOMARKER RESEARCH
Description

EXPLORATORY BIOMARKER RESEARCH

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

informed consent biomarker

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0005516
Date of Assessment Serum Biomarkers
Description

Date of Assessment Serum Biomarkers

Type de données

date

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C0229671
UMLS CUI [1,3]
C0005516

Similar models

Exploratory Biomarker Research Week 24

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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 Serum Biomarkers
Item
Date of Assessment Serum Biomarkers
date
C2985720 (UMLS CUI [1,1])
C0229671 (UMLS CUI [1,2])
C0005516 (UMLS CUI [1,3])

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