ID
41973
Description
Study ID: 110159 Clinical Study ID: 110159 Study Title: A Randomised, Double-Blind, Placebo-Controlled, 3-Period Crossover Study to Assess the Efficacy and Safety of Single Dose Intranasal GSK1004723 Compared With Placebo in an Allergen Challenge Chamber in Male Subjects With Seasonal Allergic Rhinitis Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00824356 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Placebo, GSK1004723 (200mg), GSK1004723 (1000mg) Study Indication: Allergic Rhinitis
Keywords
Versions (1)
- 3/2/21 3/2/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
March 2, 2021
DOI
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License
Creative Commons BY 4.0
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Efficacy and Safety of Single Dose Intranasal GSK1004723 in an Allergen Challenge Chamber NCT00824356
Follow-Up - Pregnancy Information; Status of Treatment Blind, Study Conclusion
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, record date/time blind broken
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C1264639
Description
Reason blind broken
Data type
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
Date of subject completion or withdrawal
Data type
date
Alias
- UMLS CUI [1]
- C2983670
Description
Was the subject withdrawn from the study?
Data type
text
Alias
- UMLS CUI [1]
- C0422727
Description
Primary reason for withdrawal
Data type
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Description
Specify Investigator discretion
Data type
text
Alias
- UMLS CUI [1,1]
- C2348235
- UMLS CUI [1,2]
- C0008961
- UMLS CUI [1,3]
- C0022423
Description
Case book ready for signature
Data type
text
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C1519316
Similar models
Follow-Up - Pregnancy Information; Status of Treatment Blind, Study Conclusion
C2347038 (UMLS CUI-2)
C1264639 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,3])
C1519316 (UMLS CUI [1,2])