ID
34362
Beschrijving
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.
Trefwoorden
Versies (2)
- 16-01-19 16-01-19 -
- 16-01-19 16-01-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
16 januari 2019
DOI
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Licentie
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
Beschrijving
Concomitant Medications
Alias
- UMLS CUI-1
- C1704627
Beschrijving
concomitant medications during study
Datatype
boolean
Alias
- UMLS CUI [1]
- C1707479
Beschrijving
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).
Datatype
text
Alias
- UMLS CUI [1]
- C2347852
Beschrijving
Dose
Datatype
float
Alias
- UMLS CUI [1]
- C2826638
Beschrijving
Unit
Datatype
text
Alias
- UMLS CUI [1]
- C2826646
Beschrijving
Frequency
Datatype
text
Alias
- UMLS CUI [1]
- C2826654
Beschrijving
Route
Datatype
text
Alias
- UMLS CUI [1]
- C2826730
Beschrijving
Start Date
Datatype
date
Maateenheden
- dd.mm.yyyy
Alias
- UMLS CUI [1]
- C2826734
Beschrijving
Started pre-study
Datatype
boolean
Alias
- UMLS CUI [1]
- C2981448
Beschrijving
Start time
Datatype
time
Maateenheden
- hh:mm
Alias
- UMLS CUI [1]
- C2826740
Beschrijving
Stop Date
Datatype
date
Maateenheden
- dd.mm.yyyy
Alias
- UMLS CUI [1]
- C2826744
Beschrijving
Ongoing Medication
Datatype
boolean
Alias
- UMLS CUI [1]
- C2826666
Beschrijving
Stop time
Datatype
time
Maateenheden
- hh:mm
Alias
- UMLS CUI [1]
- C2826659
Beschrijving
Reason for Medication
Datatype
text
Alias
- UMLS CUI [1]
- C2826696
Beschrijving
drug administered for an adverse event
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2826696
- UMLS CUI [1,2]
- C0877248
Similar models
Concomitant Medications
- StudyEvent: ODM
C0877248 (UMLS CUI [1,2])