ID

23624

Descrição

Study part: Adverse Events Week 12. 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.

Palavras-chave

  1. 10/07/2017 10/07/2017 -
Titular dos direitos

GlaxoSmithKline

Transferido a

10 de julho de 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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Adverse Events Week 12 Mepolizumab HES NCT00086658

Adverse Events Week 12

  1. StudyEvent: ODM
    1. Adverse Events Week 12
ADVERSE EVENTS
Descrição

ADVERSE EVENTS

Alias
UMLS CUI-1
C0877248
Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
Descrição

Adverse Events

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0877248

Similar models

Adverse Events Week 12

  1. StudyEvent: ODM
    1. Adverse Events Week 12
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Adverse Events
Item
Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
boolean
C0877248 (UMLS CUI [1])

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