ID

23752

Beskrivning

Study part: Adverse Events Week 20. 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.

Nyckelord

Versioner (1)
  1. 2017-07-12 2017-07-12 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

12 juli 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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Adverse Events Week 20 Mepolizumab HES NCT00086658

Engelsk

Adverse Events Week 20

1 Formulär  
  1. StudyEvent: ODM
    1. Adverse Events Week 20
ADVERSE EVENTS
Beskrivning

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?
Beskrivning

Adverse Events

Datatyp

boolean

Alias
UMLS CUI [1]
C0877248
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Similar models

Adverse Events Week 20

1 Formulär
  1. StudyEvent: ODM
    1. Adverse Events Week 20
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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