ID
34380
Beskrivning
Study ID: 101682 Clinical Study ID: B2E101682 Study Title: A randomised, double-blind, placebo-controlled, parallel group study to examine the safety, tolerability, and pharmacokinetics of repeat inhaled doses of GSK159797 in healthy subjects. Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: milveterol Study Indication: Pulmonary Disease, Chronic Obstructive.
Nyckelord
Versioner (1)
- 2019-01-17 2019-01-17 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
17 januari 2019
DOI
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Licens
Creative Commons BY-NC 3.0
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Safety, tolerability and pharmacokinetics of repeat inhaled doses of milveterol in healthy subjects (Study ID: 101682)
End of Study Record
- StudyEvent: ODM
Beskrivning
Status of treatment blind
Alias
- UMLS CUI-1
- C0749659
- UMLS CUI-2
- C2347038
Beskrivning
If YES, complete the following.
Datatyp
boolean
Alias
- UMLS CUI [1]
- C3897431
Beskrivning
Date of subject unblinding event
Datatyp
date
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
Beskrivning
Time of subject unblinding event
Datatyp
time
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0040223
Beskrivning
Reason of subject unblinding event
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0566251
Beskrivning
Specify 'Other' reason for subject unblinding event
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205394
Beskrivning
End of Study Record
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C0444930
Beskrivning
Date of subject completion or discontinuation from the study
Datatyp
date
Måttenheter
- dd.mm.yyyy
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C0011008
Beskrivning
Time of subject completion or discontinuation from the study
Datatyp
time
Måttenheter
- hh:mm
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C0040223
Beskrivning
premature discontinuation of study
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C1279919
Beskrivning
Record details on NON-SERIOUS ADVERSE EVENTS or SERIOUS ADVERSE EVENT page as appropriate.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C2348577
- UMLS CUI [1,3]
- C1279919
Beskrivning
Specification reason for discontinuation
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C2348577
- UMLS CUI [1,4]
- C1279919
Beskrivning
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Beskrivning
Date of comment
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0947611
- UMLS CUI [1,2]
- C0011008
Beskrivning
CRF page number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1704732
- UMLS CUI [1,2]
- C1516308
Beskrivning
Comment
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0947611
Beskrivning
Investigator's statement: I confirm that I have carefully examined all entries on the Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, correct as of the date below.
Alias
- UMLS CUI-1
- C1516308
- UMLS CUI-2
- C1955348
- UMLS CUI-3
- C4288115
- UMLS CUI-4
- C2349182
Beskrivning
Date of Investigator's signature
Datatyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beskrivning
Investigator's signature
Datatyp
text
Alias
- UMLS CUI [1]
- C2346576
Beskrivning
Investigator's name - print
Datatyp
text
Alias
- UMLS CUI [1]
- C2826892
Similar models
End of Study Record
- StudyEvent: ODM
C2347038 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C1279919 (UMLS CUI [1,2])
C2348577 (UMLS CUI [1,2])
C1279919 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C2348577 (UMLS CUI [1,3])
C1279919 (UMLS CUI [1,4])
C0947611 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C1516308 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C1955348 (UMLS CUI-2)
C4288115 (UMLS CUI-3)
C2349182 (UMLS CUI-4)
C0011008 (UMLS CUI [1,2])