ID

23829

Beschrijving

Study part: Concomitant Medications Week 38/ Early Withdrawal visit. 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

  1. 7/14/17 7/14/17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

July 14, 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Concomitant Medications Week 38 Mepolizumab HES NCT00086658

Concomitant Medications Week 38

CONCOMITANT MEDICATIONS
Beschrijving

CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
Are changes to the subject’s concomitant medications or any new medications taken since the last visit in the appropriate Concomitant Medications recorded?
Beschrijving

Concomitant Medications

Datatype

boolean

Alias
UMLS CUI [1]
C2347852

Similar models

Concomitant Medications Week 38

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
Concomitant Medications
Item
Are changes to the subject’s concomitant medications or any new medications taken since the last visit in the appropriate Concomitant Medications recorded?
boolean
C2347852 (UMLS CUI [1])

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