ID

23831

Description

Study part: Adverse Events 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.

Keywords

  1. 7/15/17 7/15/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 15, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Adverse Events Week 38 Mepolizumab HES NCT00086658

Adverse Events Week 38

  1. StudyEvent: ODM
    1. Adverse Events Week 38
ADVERSE EVENTS
Description

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?
Description

Adverse Events

Data type

boolean

Alias
UMLS CUI [1]
C0877248

Similar models

Adverse Events Week 38

  1. StudyEvent: ODM
    1. Adverse Events Week 38
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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