ID
34380
Descripción
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.
Palabras clave
Versiones (1)
- 17/1/19 17/1/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
17 de enero de 2019
DOI
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Licencia
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
Descripción
Status of treatment blind
Alias
- UMLS CUI-1
- C0749659
- UMLS CUI-2
- C2347038
Descripción
If YES, complete the following.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3897431
Descripción
Date of subject unblinding event
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
Descripción
Time of subject unblinding event
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0040223
Descripción
Reason of subject unblinding event
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0566251
Descripción
Specify 'Other' reason for subject unblinding event
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205394
Descripción
End of Study Record
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C0444930
Descripción
Date of subject completion or discontinuation from the study
Tipo de datos
date
Unidades de medida
- dd.mm.yyyy
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C0011008
Descripción
Time of subject completion or discontinuation from the study
Tipo de datos
time
Unidades de medida
- hh:mm
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C0040223
Descripción
premature discontinuation of study
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2348577
- UMLS CUI [1,2]
- C1279919
Descripción
Record details on NON-SERIOUS ADVERSE EVENTS or SERIOUS ADVERSE EVENT page as appropriate.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C2348577
- UMLS CUI [1,3]
- C1279919
Descripción
Specification reason for discontinuation
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C2348577
- UMLS CUI [1,4]
- C1279919
Descripción
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Descripción
Date of comment
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0947611
- UMLS CUI [1,2]
- C0011008
Descripción
CRF page number
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1704732
- UMLS CUI [1,2]
- C1516308
Descripción
Comment
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0947611
Descripción
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
Descripción
Date of Investigator's signature
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Descripción
Investigator's signature
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator's name - print
Tipo de datos
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])