ID

23618

Description

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.

Keywords

Hypereosinophilic Syndrome

7/10/17 7/10/17 -

Copyright Holder

GlaxoSmithKline

Uploaded on

July 10, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Adverse Events Weeks 9- 11 Mepolizumab HES NCT00086658

model
Details

Adverse Events Weeks 9- 11

StudyEvent: ODM
1. Adverse Events Weeks 9- 11

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

Yes

No

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Adverse Events Weeks 9- 11

StudyEvent: ODM
1. Adverse Events Weeks 9- 11

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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