ID
39862
Description
Study ID: 110852 Clinical Study ID: 110852 Study Title: MD7110852, A Phase 2b Dose-Ranging Study of Pazopanib Eye Drops versus Ranibizumab Intravitreal Injections for the Treatment of Neovascular Age-Related Macular Degeneration Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01134055 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: pazopanib eye drops, ranibizumab intravitreal injection, placebo Trade Name: pazopanib, ranibizumab Study Indication: Macular Degeneration
Keywords
Versions (1)
- 2/24/20 2/24/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
February 24, 2020
DOI
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License
Creative Commons BY-NC 4.0
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Pazopanib Eye Drops versus Ranibizumab Intravitreal Injections for the Treatment of Neovascular Age-Related Macular Degeneration NCT01134055
Subject Logs - Medical/ Surgical Procedures; Expanded/ Additional Pharmacogenetic Research Consent and Withdrawal
Description
Expanded/ Additional Pharmacogenetic Research Consent
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C2347500
- UMLS CUI-3
- C1524062
Description
Has informed consent been obtained for expanded/additional PGx research?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1524062
Description
Date informed consent obtained for expanded/additional PGx research
Data type
date
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1524062
- UMLS CUI [2]
- C0011008
Description
Has sample been collected for expanded/additional PGx research?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Description
Record date sample taken
Data type
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0011008
Description
If informed consent has not been obtained for expanded/additional PGx research, check reason
Data type
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1524062
- UMLS CUI [1,4]
- C0392360
Description
If other reason informed consent has not been obtained for expanded/additional PGx research, specify
Data type
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1524062
- UMLS CUI [1,4]
- C0392360
- UMLS CUI [2]
- C0205394
- UMLS CUI [3]
- C2348235
Description
Sample Type
Data type
text
Alias
- UMLS CUI [1]
- C2347029
Description
Expanded/ Additional Pharmacogenetic Research Withdrawal
Alias
- UMLS CUI-1
- C2349954
- UMLS CUI-2
- C2347500
- UMLS CUI-3
- C1524062
Description
Has subject withdrawn consent for expanded/additional PGx research?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1524062
Description
Date informed consent withdrawn
Data type
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Description
Has a request been made for sample destruction?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Description
Check reason for request for sample destruction?
Data type
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [2]
- C0392360
Description
Sample type
Data type
text
Alias
- UMLS CUI [1]
- C2347029
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C1524062 (UMLS CUI [1,3])
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C2347500 (UMLS CUI-2)
C1524062 (UMLS CUI-3)
C2347500 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
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