ID

23841

Beschrijving

Study part: Central Laboratory –Blood and Urine 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.

Trefwoorden

  1. 15-07-17 15-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

15 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Central Laboratory –Blood and Urine Week 38 Mepolizumab HES NCT00086658

Central Laboratory –Blood and Urine Week 38

CENTRAL LABORATORY - BLOOD AND URINE
Beschrijving

CENTRAL LABORATORY - BLOOD AND URINE

Alias
UMLS CUI-1
C1880016
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Date sample taken
Beschrijving

Date sample taken

Datatype

date

Alias
UMLS CUI [1]
C1302413

Similar models

Central Laboratory –Blood and Urine Week 38

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
CENTRAL LABORATORY - BLOOD AND URINE
C1880016 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Date sample taken
Item
Date sample taken
date
C1302413 (UMLS CUI [1])

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