ID
36583
Descripción
Study ID: 109609 Clinical Study ID: 109609 Study Title: A Phase II, Non-randomized, Multi-center Study to Evaluate the Efficacy and Safety of Pazopanib (GW786034) in Subjects With Advanced Non-Small Cell Lung Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00549328 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GW786034 Trade Name: Drug: Pazopanib Study Indication: Lung Cancer, Non-Small Cell
Palabras clave
Versiones (1)
- 23/5/19 23/5/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
23 de mayo de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Efficacy and Safety of Pazopanib (GW786034) in Subjects With Advanced Non-Small Cell Lung Cancer NCT00549328
Death; Study Conclusion; Pharmacogenetic Research Withdrawal of Consent; Pregnancy Information; Investigatoinal Product Discontinuation; Investigational Product Compliance - Pazopanib; Log Status
Descripción
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Descripción
Date of subject completion or date of subject withdrawal
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2983670
- UMLS CUI [2,1]
- C1710677
- UMLS CUI [2,2]
- C0011008
Descripción
Was the subject withdrawn from the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0422727
Descripción
If subject was withdrawn from study, select primary reson for withdrawal
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
Descripción
If other reason for withdrawal, please specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
For Data Managers or Monitors only By ticking or unticking this box you are evoking a change to this form that will invalidate the original signature and will revert the form back to an unsigned state. This should be done when significant changes (e.g. those that require medical opinion or other significant situations) occur after the original signature. If the box is already ticked upon arrival on this form, unticking and submitting it accomplishes the same task as ticking and submitting it; that is, the signature will be in validated in both instances.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C2346576
Descripción
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Descripción
Has subject withdrawn consent for PGx research?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Descripción
If subject has withdrawn consent for PGx research, enter date informed consent withdrawn.
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
- UMLS CUI [1,3]
- C0011008
Descripción
Has a request been made for blood sample destruction?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Descripción
If a request has been made for blood sample destruction, check reason
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
Descripción
If other reason for request for blood sample destruction, please specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
- UMLS CUI [1,5]
- C0205394
- UMLS CUI [1,6]
- C2348235
Descripción
Sample type
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2347029
Descripción
Genetics Type
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0017399
- UMLS CUI [1,2]
- C0332307
Descripción
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descripción
Investigational Product Discontinuation
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0457454
Descripción
Give primary reason Investigational Product was discontinued permanently
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
Descripción
If other primary reason Investigational Product was discontinued permanently, please specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Investigational Product Compliance
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Descripción
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Descripción
Did the subject experience any non-serious adverse events during the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1518404
Descripción
Were any concomitant medications taken by the subject during the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2347852
Descripción
Did the subject experience a serious adverse event during the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1519255
Descripción
Any blood products taken?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0456388
Descripción
Has subject had surgery/procedure?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0543467
- UMLS CUI [2]
- C0199171
Similar models
Death; Study Conclusion; Pharmacogenetic Research Withdrawal of Consent; Pregnancy Information; Investigatoinal Product Discontinuation; Investigational Product Compliance - Pazopanib; Log Status
C2348568 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C1710677 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C1549995 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0031325 (UMLS CUI-2)
C0031325 (UMLS CUI [1,2])
C0031325 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C0205394 (UMLS CUI [1,5])
C2348235 (UMLS CUI [1,6])
C0332307 (UMLS CUI [1,2])
C0457454 (UMLS CUI-2)
C1549995 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C1321605 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0332156 (UMLS CUI [1,3])
C0039225 (UMLS CUI [1,2])
C0199171 (UMLS CUI [2])