ID
41302
Description
Study ID: 103471 Clinical Study ID: 103471 Study Title: A randomised, double blind, placebo-controlled, double dummy, five-way cross over dose-escalation study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single inhaled doses of GSK233705 (20-500µg via DPI), and, tiotropium bromide (18µg via DPI) in healthy male subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Darotropium Bromide Trade Name: Darotropium Bromide Study Indication: Chronic Obstructive Pulmonary Disease (COPD)
Keywords
Versions (1)
- 8/12/20 8/12/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
August 12, 2020
DOI
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License
Creative Commons BY 4.0
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Safety, tolerability, pharmacokinetics and pharmacodynamics of GSK233705 and tiotropium bromide (103471)
Laboratory Result Data; Urinalysis
- StudyEvent: ODM
Description
Laboratory Result data (Haematology) - 12 Hrs Post-Dose (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0474523
- UMLS CUI-3
- C0439568
Description
Date and time sample taken (Haematology)
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [1,4]
- C0018941
Description
Has the subject fasted?
Data type
boolean
Alias
- UMLS CUI [1]
- C0015663
Description
Haematology Test (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0018941
Description
Haematology Test
Data type
integer
Alias
- UMLS CUI [1]
- C0018941
Description
Haematology Test Result
Data type
text
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2]
- C0587081
Description
Urinalysis - 12 hrs Post-Dose (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0439568
Description
Urinalysis (Dipstick) Test - 12 hrs (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0430370
Description
Urinalysis (Dipstick) Test
Data type
integer
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
Description
Urinalysis (Dipstick) Test Result
Data type
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
- UMLS CUI [2]
- C0587081
Description
Urinalysis (Microscopy) Test
Data type
integer
Alias
- UMLS CUI [1]
- C0430397
Description
Urinalysis (Microscopy) Test Result
Data type
text
Alias
- UMLS CUI [1]
- C0430397
- UMLS CUI [2]
- C0587081
Description
Laboratory Result Data (Haematology) - 24 hrs Post-Dose (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0474523
- UMLS CUI-3
- C0439568
Description
Date and time sample taken (Haematology)
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [1,4]
- C0018941
Description
Has the subject fasted?
Data type
boolean
Alias
- UMLS CUI [1]
- C0015663
Description
Haematology Test - 24 hrs Post-Dose (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0018941
Description
Haematology Test
Data type
integer
Alias
- UMLS CUI [1]
- C0018941
Description
Haematology Test Result
Data type
text
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2]
- C0587081
Description
Urinalysis - 24 hrs Post-Dose (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0439568
Description
Urinalysis (Dipstick) Test - 24 hrs (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0430370
Description
Urinalysis (Dipstick) Test
Data type
integer
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
Description
Urinalysis (Dipstick) Test - 24 hrs (Treatment Period 1, 2, 3, 4, 5)
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0430370
Description
Urinalysis (Dipstick) Test
Data type
integer
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
Description
Urinalysis (Dipstick) Test Result
Data type
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
- UMLS CUI [2]
- C0587081
Description
Urinalysis (Microscopy) Test
Data type
integer
Alias
- UMLS CUI [1]
- C0430397
Description
Urinalysis (Microscopy) Test Result
Data type
text
Alias
- UMLS CUI [1]
- C0430397
- UMLS CUI [2]
- C0587081
Similar models
Laboratory Result Data; Urinalysis
- StudyEvent: ODM
C0474523 (UMLS CUI-2)
C0439568 (UMLS CUI-3)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0018941 (UMLS CUI [1,4])
C0587081 (UMLS CUI [2])
C0439568 (UMLS CUI-2)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0042014 (UMLS CUI [2])
C0430370 (UMLS CUI-2)
C0430370 (UMLS CUI [1,2])
C0430370 (UMLS CUI [1,2])
C0587081 (UMLS CUI [2])
C0587081 (UMLS CUI [2])
C0474523 (UMLS CUI-2)
C0439568 (UMLS CUI-3)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0018941 (UMLS CUI [1,4])
C0587081 (UMLS CUI [2])
C0439568 (UMLS CUI-2)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0042014 (UMLS CUI [2])
C0430370 (UMLS CUI-2)
C0430370 (UMLS CUI [1,2])
C0430370 (UMLS CUI-2)
C0430370 (UMLS CUI [1,2])
C0430370 (UMLS CUI [1,2])
C0587081 (UMLS CUI [2])
C0587081 (UMLS CUI [2])
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