ID

23618

Beschrijving

Study part: Adverse Events Weeks 9- 11. 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.

Trefwoorden

  1. 10-07-17 10-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

10 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Adverse Events Weeks 9- 11 Mepolizumab HES NCT00086658

Adverse Events Weeks 9- 11

ADVERSE EVENTS
Beschrijving

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?
Beschrijving

Adverse Events

Datatype

boolean

Alias
UMLS CUI [1]
C0877248

Similar models

Adverse Events Weeks 9- 11

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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