0 Beoordelingen

ID

22722

Beschrijving

Study part: Adverse Events Run-In Visits. 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

11-06-17 11-06-17 -

Houder van rechten

GlaxoSmithKline

Geüploaded op

11 juni 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Adverse Events Run-In Visits Mepolizumab HES NCT00086658

model
Details

Adverse Events Run-In Visits

StudyEvent: ODM
1. Adverse Events Run-In Visits

ADVERSE EVENTS

Beschrijving

ADVERSE EVENTS

Alias

UMLS CUI-1: C0877248 (Adverse event)
LOINC: MTHU014542

AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?

Beschrijving

Adverse Events

Datatype

boolean

Alias

UMLS CUI [1]: C0877248 (Adverse event)
LOINC: MTHU014542

Yes

No

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Adverse Events Run-In Visits

StudyEvent: ODM
1. Adverse Events Run-In Visits

Name

Type

Description | Question | Decode (Coded Value)

Datatype

Alias

Item Group

ADVERSE EVENTS

C0877248 (UMLS CUI-1)

Adverse Events

Item

AE's and SAE's related to study participation during the screening and Prednisone stabilization period reported?

boolean

C0877248 (UMLS CUI [1])

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