ID
36583
Beschrijving
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
Trefwoorden
Versies (1)
- 23-05-19 23-05-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
23 mei 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 3.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
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
Beschrijving
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschrijving
Date of subject completion or date of subject withdrawal
Datatype
date
Alias
- UMLS CUI [1]
- C2983670
- UMLS CUI [2,1]
- C1710677
- UMLS CUI [2,2]
- C0011008
Beschrijving
Was the subject withdrawn from the study?
Datatype
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschrijving
If subject was withdrawn from study, select primary reson for withdrawal
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
Beschrijving
If other reason for withdrawal, please specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschrijving
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.
Datatype
integer
Alias
- UMLS CUI [1]
- C2346576
Beschrijving
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Beschrijving
Has subject withdrawn consent for PGx research?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Beschrijving
If subject has withdrawn consent for PGx research, enter date informed consent withdrawn.
Datatype
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
- UMLS CUI [1,3]
- C0011008
Beschrijving
Has a request been made for blood sample destruction?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Beschrijving
If a request has been made for blood sample destruction, check reason
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
Beschrijving
If other reason for request for blood sample destruction, please specify
Datatype
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
Beschrijving
Sample type
Datatype
text
Alias
- UMLS CUI [1]
- C2347029
Beschrijving
Genetics Type
Datatype
text
Alias
- UMLS CUI [1,1]
- C0017399
- UMLS CUI [1,2]
- C0332307
Beschrijving
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Beschrijving
Investigational Product Discontinuation
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0457454
Beschrijving
Give primary reason Investigational Product was discontinued permanently
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
Beschrijving
If other primary reason Investigational Product was discontinued permanently, please specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschrijving
Investigational Product Compliance
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Beschrijving
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Beschrijving
Did the subject experience any non-serious adverse events during the study?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1518404
Beschrijving
Were any concomitant medications taken by the subject during the study?
Datatype
boolean
Alias
- UMLS CUI [1]
- C2347852
Beschrijving
Did the subject experience a serious adverse event during the study?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
Any blood products taken?
Datatype
boolean
Alias
- UMLS CUI [1]
- C0456388
Beschrijving
Has subject had surgery/procedure?
Datatype
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])