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

Hypereosinophilic Syndrome

10-07-17 10-07-17 -

Houder van rechten

GlaxoSmithKline

Geüploaded op

10 juli 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

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

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

Terug naar het begin van de pagina

Similar models

Show recommended models

Adverse Events Weeks 9- 11

StudyEvent: ODM
1. 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])

Terug naar het begin van de pagina

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.