ID
36583
Beschreibung
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
Stichworte
Versionen (1)
- 23.05.19 23.05.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
23. Mai 2019
DOI
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Lizenz
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
Beschreibung
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschreibung
Date of subject completion or date of subject withdrawal
Datentyp
date
Alias
- UMLS CUI [1]
- C2983670
- UMLS CUI [2,1]
- C1710677
- UMLS CUI [2,2]
- C0011008
Beschreibung
Was the subject withdrawn from the study?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschreibung
If subject was withdrawn from study, select primary reson for withdrawal
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
Beschreibung
If other reason for withdrawal, please specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschreibung
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.
Datentyp
integer
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Beschreibung
Has subject withdrawn consent for PGx research?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Beschreibung
If subject has withdrawn consent for PGx research, enter date informed consent withdrawn.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
- UMLS CUI [1,3]
- C0011008
Beschreibung
Has a request been made for blood sample destruction?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Beschreibung
If a request has been made for blood sample destruction, check reason
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
Beschreibung
If other reason for request for blood sample destruction, please specify
Datentyp
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
Beschreibung
Sample type
Datentyp
text
Alias
- UMLS CUI [1]
- C2347029
Beschreibung
Genetics Type
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0017399
- UMLS CUI [1,2]
- C0332307
Beschreibung
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Beschreibung
Investigational Product Discontinuation
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0457454
Beschreibung
Give primary reason Investigational Product was discontinued permanently
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
Beschreibung
If other primary reason Investigational Product was discontinued permanently, please specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C4288399
- UMLS CUI [1,2]
- C1549995
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschreibung
Investigational Product Compliance
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Beschreibung
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Beschreibung
Did the subject experience any non-serious adverse events during the study?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1518404
Beschreibung
Were any concomitant medications taken by the subject during the study?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2347852
Beschreibung
Did the subject experience a serious adverse event during the study?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschreibung
Any blood products taken?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0456388
Beschreibung
Has subject had surgery/procedure?
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0543467
- UMLS CUI [2]
- C0199171
Ähnliche Modelle
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])