ID

23842

Descripción

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.

Palabras clave

Versiones (1)
  1. 15/7/17 15/7/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

15 de julio de 2017

DOI

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Licencia

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

Inglés

Exploratory Biomarker Research Week 38

1 formularios  
EXPLORATORY BIOMARKER RESEARCH
Descripción

EXPLORATORY BIOMARKER RESEARCH

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

informed consent biomarker

Tipo de datos

boolean

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

Date of Assessment

Tipo de datos

date

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

Date of Assessment Skin Biopsy

Tipo de datos

date

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

Date of Assessment GI Biopsy

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C0005558
UMLS CUI [1,3]
C0017189
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Similar models

Exploratory Biomarker Research Week 38

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página 

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