ID
34362
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. This form contains information about concomitant medications and should be completed only in case of concomitant medication.
Nyckelord
Versioner (2)
- 2019-01-16 2019-01-16 -
- 2019-01-16 2019-01-16 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
16 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)
Concomitant Medications
- StudyEvent: ODM
Beskrivning
Concomitant Medications
Alias
- UMLS CUI-1
- C1704627
Beskrivning
concomitant medications during study
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1707479
Beskrivning
If medication is given to treat an adverse event, then the ADVERSE EVENT must be recorded on the NON-SERIOUS ADVERSE EVENT or SERIOUS ADVERSE EVENT page(s).
Datatyp
text
Alias
- UMLS CUI [1]
- C2347852
Beskrivning
Dose
Datatyp
float
Alias
- UMLS CUI [1]
- C2826638
Beskrivning
Unit
Datatyp
text
Alias
- UMLS CUI [1]
- C2826646
Beskrivning
Frequency
Datatyp
text
Alias
- UMLS CUI [1]
- C2826654
Beskrivning
Route
Datatyp
text
Alias
- UMLS CUI [1]
- C2826730
Beskrivning
Start Date
Datatyp
date
Måttenheter
- dd.mm.yyyy
Alias
- UMLS CUI [1]
- C2826734
Beskrivning
Started pre-study
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2981448
Beskrivning
Start time
Datatyp
time
Måttenheter
- hh:mm
Alias
- UMLS CUI [1]
- C2826740
Beskrivning
Stop Date
Datatyp
date
Måttenheter
- dd.mm.yyyy
Alias
- UMLS CUI [1]
- C2826744
Beskrivning
Ongoing Medication
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
Stop time
Datatyp
time
Måttenheter
- hh:mm
Alias
- UMLS CUI [1]
- C2826659
Beskrivning
Reason for Medication
Datatyp
text
Alias
- UMLS CUI [1]
- C2826696
Beskrivning
drug administered for an adverse event
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2826696
- UMLS CUI [1,2]
- C0877248
Similar models
Concomitant Medications
- StudyEvent: ODM
C0877248 (UMLS CUI [1,2])