ID

22955

Description

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

Keywords

  1. 6/18/17 6/18/17 -
Uploaded on

June 18, 2017

DOI

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License

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
Description

Investigator Comment Log

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

Date of comment

Data type

date

Measurement units
  • dd.mm.yyyy
Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C0011008
dd.mm.yyyy
Comment
Description

Comment

Data type

text

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

CRF page number

Data type

integer

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

Investigators signature

Data type

text

Alias
UMLS CUI [1]
C2346576
Investigators name
Description

Investigators name

Data type

text

Alias
UMLS CUI [1]
C2826892
Date
Description

Date of report

Data type

date

Measurement units
  • 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)
Data type
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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