ID
38620
Description
Study ID: 111610 Clinical Study ID: 111610 Study Title: A randomised, double-blind, placebo-controlled study in healthy volunteers to examine the safety, tolerability and pharmacokinetics of a) single, ascending and b) twice-daily repeat doses of intranasal SB-705498. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00907933 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: SB705498, Placebo Study Indication: Rhinitis
Keywords
Versions (1)
- 10/28/19 10/28/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 28, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Safety, tolerability and pharmacokinetics of single, ascending and twice-daily repeat doses of intranasal SB-705498 NCT00907933
Follow-Up - Dateof Visit; Status of Treatment Blind; Study Conclusion; Pregnancy Information
Description
Status of Treatment Blind
Alias
- UMLS CUI-1
- C0749659
- UMLS CUI-2
- C2347038
Description
If yes, complete the Adverse Event form and/or Investigational Product forms as appropriate.
Data type
boolean
Alias
- UMLS CUI [1]
- C3897431
Description
If treatment blind was broken during the study, enter date/ time blind broken.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C3897431
- UMLS CUI [2,2]
- C0040223
Description
Reason blind broken
Data type
integer
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
Description
If other reason blind broken, please specify
Data type
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
Date of last contact
Data type
date
Alias
- UMLS CUI [1]
- C0805839
Description
Was the subject withdrawn from the study?
Data type
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
If subject was withdrawn from study, please record date of decision to withdraw
Data type
date
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
- UMLS CUI [1,3]
- C0011008
Description
Primary reason for withdrawal
Data type
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Description
If investigator discretion, please specify
Data type
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0022423
- UMLS CUI [1,3]
- C2348235
Description
Pregnancy Information (Preg F)
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Description
Pregnancy Information (Preg M)
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Similar models
Follow-Up - Dateof Visit; Status of Treatment Blind; Study Conclusion; Pregnancy Information
C2985720 (UMLS CUI [1,2])
C2347038 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C3897431 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C1533716 (UMLS CUI-2)
C1533716 (UMLS CUI-2)