ID
41166
Beschrijving
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)
Trefwoorden
Versies (1)
- 03-07-20 03-07-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
3 juli 2020
DOI
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Licentie
Creative Commons BY 4.0
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Safety, tolerability, pharmacokinetics and pharmacodynamics of GSK233705 and tiotropium bromide (103471)
Drug and Alcohol Screen; Laboratory Result Data; Urinalysis
- StudyEvent: ODM
Beschrijving
Drug and alcohol screen
Alias
- UMLS CUI-1
- C0202274
- UMLS CUI-2
- C0202304
Beschrijving
Drug and alcohol screen
Alias
- UMLS CUI-1
- C0202274
- UMLS CUI-2
- C0202304
Beschrijving
Substance
Datatype
integer
Alias
- UMLS CUI [1]
- C0439861
Beschrijving
Drug and alcohol test finding
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0202274
- UMLS CUI [1,2]
- C0202304
- UMLS CUI [1,3]
- C0587081
Beschrijving
Laboratory Result Data (Haematology)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0474523
Beschrijving
Date and time sample taken (Haematology)
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0200345
- UMLS CUI [2]
- C0018941
Beschrijving
Has the subject fasted? (Haematology)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0015663
- UMLS CUI [2]
- C0018941
Beschrijving
Laboratory Result Data (Haematology)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0474523
Beschrijving
Haematology test
Datatype
integer
Alias
- UMLS CUI [1]
- C0018941
Beschrijving
Test Result (Haematology)
Datatype
text
Alias
- UMLS CUI [1]
- C0587081
- UMLS CUI [2]
- C0018941
Beschrijving
Laboratory Result Data (Clinical Chemistry)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
- UMLS CUI-3
- C1274040
Beschrijving
Date and time sample taken (Clinical Chemistry)
Datatype
datetime
Alias
- UMLS CUI [1]
- C0008000
- UMLS CUI [2,1]
- C0200345
- UMLS CUI [2,2]
- C0011008
- UMLS CUI [2,3]
- C0040223
Beschrijving
Has the subject fasted? (Clinical Chemistry)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0015663
- UMLS CUI [2]
- C0008000
Beschrijving
Laboratory Result Data (Clinical Chemistry)
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0008000
- UMLS CUI-3
- C1274040
Beschrijving
Clinical Chemistry Test
Datatype
integer
Alias
- UMLS CUI [1]
- C0525044
Beschrijving
Test Result (Clinical Chemistry)
Datatype
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0587081
Beschrijving
Urinalysis
Alias
- UMLS CUI-1
- C0042014
Beschrijving
Urinalysis (Dipstick) Test
Alias
- UMLS CUI-1
- C0042014
- UMLS CUI-2
- C0430370
Beschrijving
Urinalysis (Dipstick) Test
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
Beschrijving
Urinalysis (Dipstick) Test Result
Datatype
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0430370
- UMLS CUI [1,3]
- C1274040
Beschrijving
Urinalysis (Microscopy) Test
Alias
- UMLS CUI-1
- C0430397
Similar models
Drug and Alcohol Screen; Laboratory Result Data; Urinalysis
- StudyEvent: ODM
C0202304 (UMLS CUI-2)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0202304 (UMLS CUI-2)
C0202304 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,3])
C0474523 (UMLS CUI-2)
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
C0018941 (UMLS CUI [2])
C0018941 (UMLS CUI [2])
C0474523 (UMLS CUI-2)
C0018941 (UMLS CUI [2])
C0008000 (UMLS CUI-2)
C1274040 (UMLS CUI-3)
C0200345 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
C0008000 (UMLS CUI [2])
C0008000 (UMLS CUI-2)
C1274040 (UMLS CUI-3)
C0587081 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0430370 (UMLS CUI-2)
C0430370 (UMLS CUI [1,2])
C0430370 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0587081 (UMLS CUI [1,2])