ID

23624

Beschrijving

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.

Trefwoorden

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 Week 12 Mepolizumab HES NCT00086658

model
Details

Adverse Events Week 12

StudyEvent: ODM
1. Adverse Events Week 12

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

Yes

No

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Adverse Events Week 12

StudyEvent: ODM
1. Adverse Events Week 12

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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