ID

22717

Descripción

Study part: Adverse Events Screening 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

  1. 11/6/17 11/6/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

11 de junio de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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Adverse Events Screening Visit Mepolizumab HES NCT00086658

Adverse Events Screening Visit

ADVERSE EVENTS
Descripción

ADVERSE EVENTS

Alias
UMLS CUI-1
C0877248
AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?
Descripción

Adverse Events

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0877248

Similar models

Adverse Events Screening Visit

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Adverse Events
Item
AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?
boolean
C0877248 (UMLS CUI [1])

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