ID

22955

Beschrijving

Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Trefwoorden

  1. 18-06-17 18-06-17 -
Geüploaded op

18 juni 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Investigator Comment Log - GSK Milveterol COPD 100527

Investigator Comment Log - GSK Milveterol COPD 100527

Investigator Comment Log
Beschrijving

Investigator Comment Log

Alias
UMLS CUI-1
C0008961
UMLS CUI-2
C0947611
Date of comment
Beschrijving

Date of comment

Datatype

date

Maateenheden
  • dd.mm.yyyy
Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C0011008
dd.mm.yyyy
Comment
Beschrijving

Comment

Datatype

text

Alias
UMLS CUI [1]
C0947611
CRF page number if applicable
Beschrijving

CRF page number

Datatype

integer

Alias
UMLS CUI [1,1]
C1704732
UMLS CUI [1,2]
C1516308
Investigators signature
Beschrijving

Investigators signature

Datatype

text

Alias
UMLS CUI [1]
C2346576
Investigators name
Beschrijving

Investigators name

Datatype

text

Alias
UMLS CUI [1]
C2826892
Date
Beschrijving

Date of report

Datatype

date

Maateenheden
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C1302584
dd.mm.yyyy

Similar models

Investigator Comment Log - GSK Milveterol COPD 100527

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Investigator Comment Log
C0008961 (UMLS CUI-1)
C0947611 (UMLS CUI-2)
Date of comment
Item
Date of comment
date
C0947611 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
CRF page number
Item
CRF page number if applicable
integer
C1704732 (UMLS CUI [1,1])
C1516308 (UMLS CUI [1,2])
Investigators signature
Item
Investigators signature
text
C2346576 (UMLS CUI [1])
Investigators name
Item
Investigators name
text
C2826892 (UMLS CUI [1])
Date of report
Item
Date
date
C1302584 (UMLS CUI [1])

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