ID

22763

Description

Study part: Pharmacokinetics- Blood Day 1 Pre-Infusion.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

Versions (1)
  1. 6/11/17 6/11/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 11, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Pharmacokinetics- Blood Day 1 Pre-Infusion Mepolizumab HES NCT00086658

English

Pharmacokinetics- Blood Day 1 Pre-Infusion

1 forms  
PHARMACOKINETICS - BLOOD
Description

PHARMACOKINETICS - BLOOD

Alias
UMLS CUI-1
C0031327 (Drug Kinetics)
UMLS CUI-2
C0005767 (Blood)
SNOMED
87612001
LOINC
LP71680-0
Planned Relative Time
Description

Planned Relative Time

Data type

time

Alias
UMLS CUI [1]
C0439564 (Relative time)
SNOMED
118578006
LOINC
LP21276-8
Date Sample Taken
Description

Date Sample Taken

Data type

date

Alias
UMLS CUI [1]
C1302413 (Specimen collection date)
SNOMED
399445004
Actual Time
Description

Actual Time

Data type

time

Alias
UMLS CUI [1]
C0040223 (Time)
SNOMED
410670007
LOINC
LP73517-2
Sample Identifier
Description

Sample Identifier

Data type

text

Alias
UMLS CUI [1]
C4071975 (undefined)
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Similar models

Pharmacokinetics- Blood Day 1 Pre-Infusion

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
PHARMACOKINETICS - BLOOD
C0031327 (UMLS CUI-1)
C0005767 (UMLS CUI-2)
Planned Relative Time
Item
Planned Relative Time
time
C0439564 (UMLS CUI [1])
Date Sample Taken
Item
Date Sample Taken
date
C1302413 (UMLS CUI [1])
Actual Time
Item
Actual Time
time
C0040223 (UMLS CUI [1])
Sample Identifier
Item
Sample Identifier
text
C4071975 (UMLS CUI [1])
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