ID

22721

Description

Study part: Prednisone Stabilisation Dose Run-In Visits.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

  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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Prednisone Stabilisation Dose Run-In Visits Mepolizumab HES NCT00086658

Prednisone Stabilisation Dose Run-In Visits

PREDNISONE STABILISATION DOSE
Description

PREDNISONE STABILISATION DOSE

Alias
UMLS CUI-1
C3174092
UMLS CUI-2
C0032952
Prednisone stabilisation dose in the Screening Corticosteriod Medition section recorded?
Description

dose prednisone

Data type

boolean

Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C0032952

Similar models

Prednisone Stabilisation Dose Run-In Visits

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
PREDNISONE STABILISATION DOSE
C3174092 (UMLS CUI-1)
C0032952 (UMLS CUI-2)
dose prednisone
Item
Prednisone stabilisation dose in the Screening Corticosteriod Medition section recorded?
boolean
C3174092 (UMLS CUI [1,1])
C0032952 (UMLS CUI [1,2])

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