ID

23752

Descrizione

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.

Keywords

12/07/17 12/07/17 -

Titolare del copyright

GlaxoSmithKline

Caricato su

12 luglio 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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Adverse Events Week 20 Mepolizumab HES NCT00086658

model
Dettagli

Adverse Events Week 20

StudyEvent: ODM
1. Adverse Events Week 20

ADVERSE EVENTS

Descrizione

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?

Descrizione

Adverse Events

Tipo di dati

boolean

Alias

UMLS CUI [1]: C0877248

Yes

No

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Adverse Events Week 20

StudyEvent: ODM
1. Adverse Events Week 20

Name

genere

Description | Question | Decode (Coded Value)

Tipo di dati

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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