ID
37662
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 Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GW786034 Trade Name: Drug: Pazopanib Study Indication: Lung Cancer, Non-Small Cell
Trefwoorden
Versies (4)
- 08-05-19 08-05-19 -
- 14-08-19 14-08-19 -
- 14-08-19 14-08-19 -
- 15-03-21 15-03-21 - Dr. rer. medic Philipp Neuhaus
Houder van rechten
GlaxoSmithKline
Geüploaded op
14 augustus 2019
DOI
Voor een aanvraag inloggen.
Licentie
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
Screening - Subject Identification; Demography; Disease Characteristics; Status at Screening; Anti-Cancer Therapy; Anti-Cancer Radiotherapy; Medical Conditions
Beschrijving
Subject number
Alias
- UMLS CUI-1
- C2348585
Beschrijving
Date of Visit/ Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Beschrijving
Local Laboratories
Alias
- UMLS CUI-1
- C0022877
- UMLS CUI-2
- C0205276
Beschrijving
If another local laboratory is used after you have already selected a response and submitted fjjjl Th the form, change your response and an additional local laboratory form will be created.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0022877
- UMLS CUI [1,2]
- C0205276
- UMLS CUI [1,3]
- C0237753
Beschrijving
Laboratory Name
Datatype
text
Alias
- UMLS CUI [1]
- C3258037
Beschrijving
Laboratory Address
Datatype
text
Alias
- UMLS CUI [1,1]
- C1442065
- UMLS CUI [1,2]
- C0022877
Beschrijving
Laboratory ID
Datatype
text
Alias
- UMLS CUI [1]
- C2986056
Beschrijving
Subject identification
Alias
- UMLS CUI-1
- C2348585
Beschrijving
Demography
Alias
- UMLS CUI-1
- C0011298
Beschrijving
Date of birth
Datatype
date
Alias
- UMLS CUI [1]
- C0421451
Beschrijving
Sex
Datatype
text
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Ethnicity
Datatype
integer
Alias
- UMLS CUI [1]
- C0015031
Beschrijving
Check all that apply
Datatype
integer
Alias
- UMLS CUI [1]
- C3841890
Beschrijving
Disease Characteristics
Alias
- UMLS CUI-1
- C1705348
Beschrijving
Primary Tumour Type at Initial Diagnosis
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0677930
- UMLS CUI [1,2]
- C0332307
- UMLS CUI [1,3]
- C4071762
Beschrijving
Date of Initial Diagnosis
Datatype
date
Alias
- UMLS CUI [1]
- C2316983
Beschrijving
Stage at Initial Diagnosis
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1300072
- UMLS CUI [1,2]
- C0011900
- UMLS CUI [1,3]
- C0205265
Beschrijving
Histology at Initial Diagnosis
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0019638
- UMLS CUI [1,2]
- C0011900
- UMLS CUI [1,3]
- C0205265
Beschrijving
Date of Last Progression
Datatype
date
Alias
- UMLS CUI [1,1]
- C0242656
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
Beschrijving
Date of Staging at Screening
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0027646
- UMLS CUI [2]
- C1710477
Beschrijving
Stage at Screening
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1300072
- UMLS CUI [1,2]
- C0220908
Beschrijving
Lines of Therapy Completed at Screening
Datatype
integer
Alias
- UMLS CUI [1]
- C1514463
Beschrijving
Metastatic Disease
Alias
- UMLS CUI-1
- C0027627
Beschrijving
Did the subject have metastatic disease at screening?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0027627
- UMLS CUI [1,2]
- C0220908
Beschrijving
If subject had metastatic disease at screening, complete date metastatic disease was first diagnosed
Datatype
date
Alias
- UMLS CUI [1,1]
- C0027627
- UMLS CUI [1,2]
- C0220908
- UMLS CUI [1,3]
- C0011008
Beschrijving
Status at Screening
Alias
- UMLS CUI-1
- C0220908
- UMLS CUI-2
- C0449438
Beschrijving
Did the subject receive prior chemo, immuno, hormonal or biologic therapies for the cancer under study?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C0920425
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [2,1]
- C0279025
- UMLS CUI [2,2]
- C0920425
- UMLS CUI [2,3]
- C0332152
- UMLS CUI [3,1]
- C1531518
- UMLS CUI [3,2]
- C0920425
- UMLS CUI [3,3]
- C0332152
- UMLS CUI [4,1]
- C0021083
- UMLS CUI [4,2]
- C0920425
- UMLS CUI [4,3]
- C0332152
Beschrijving
Did the subject receive prior radiotherapy for the cancer under study?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C0920425
- UMLS CUI [1,3]
- C0332152
Beschrijving
Has subject had prior surgery/ procedure?
Datatype
boolean
Alias
- UMLS CUI [1]
- C0744961
Beschrijving
Were any concomitant medications taken by the subject prior to screening?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C0220908
Beschrijving
Anti-Cancer Therapy
Alias
- UMLS CUI-1
- C0920425
Beschrijving
Sequence Number
Datatype
integer
Alias
- UMLS CUI [1]
- C2348184
Beschrijving
(Trade Name preferred)
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
Modified reported term
Datatype
text
Alias
- UMLS CUI [1]
- C2826302
Beschrijving
GSK Drug synonym
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0871468
Beschrijving
GSR Drug Collection code
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1516698
- UMLS CUI [1,3]
- C0805701
Beschrijving
Failed coding
Datatype
text
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Beschrijving
Regimen Sequence
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1276413
- UMLS CUI [1,2]
- C2348184
Beschrijving
Therapy Type
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0087111
Beschrijving
Number of Cycles/Doses
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0750480
Beschrijving
Units
Datatype
integer
Alias
- UMLS CUI [1]
- C1519795
Beschrijving
Intent
Datatype
integer
Alias
- UMLS CUI [1]
- C1283828
Beschrijving
Therapy Start Date
Datatype
date
Alias
- UMLS CUI [1]
- C1531783
Beschrijving
Therapy Stop Date
Datatype
date
Alias
- UMLS CUI [1]
- C1531784
Beschrijving
Best Response
Datatype
integer
Alias
- UMLS CUI [1]
- C2986560
Beschrijving
Duration of Response
Datatype
durationDatetime
Maateenheden
- Weeks
Alias
- UMLS CUI [1]
- C0237585
Beschrijving
Anti-Cancer Therapy
Alias
- UMLS CUI-1
- C0920425
Beschrijving
Sequence Number
Datatype
integer
Alias
- UMLS CUI [1]
- C2348184
Beschrijving
Site
Datatype
text
Alias
- UMLS CUI [1]
- C2825164
Beschrijving
Cumulative Dose
Datatype
float
Alias
- UMLS CUI [1]
- C2986497
Beschrijving
Units
Datatype
integer
Alias
- UMLS CUI [1]
- C1519795
Beschrijving
Intent
Datatype
integer
Alias
- UMLS CUI [1]
- C1283828
Beschrijving
Radiotherapy Start Date
Datatype
date
Alias
- UMLS CUI [1]
- C0436382
Beschrijving
Radiotherapy Stop Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C0806020
Beschrijving
Best Response
Datatype
integer
Alias
- UMLS CUI [1]
- C2986560
Beschrijving
Duration of Response
Datatype
durationDatetime
Maateenheden
- Weeks
Alias
- UMLS CUI [1]
- C0237585
Beschrijving
Medical Conditions
Alias
- UMLS CUI-1
- C0012634
Beschrijving
Sequence Number
Datatype
integer
Alias
- UMLS CUI [1]
- C2348184
Beschrijving
Specific Condition
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C2348235
Beschrijving
Modified Term
Datatype
text
Alias
- UMLS CUI [1]
- C2826302
Beschrijving
MedDRA Synonym
Datatype
text
Alias
- UMLS CUI [1]
- C1140263
Beschrijving
MedDRA lower level term code
Datatype
text
Alias
- UMLS CUI [1]
- C3898442
Beschrijving
Failed coding
Datatype
text
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Beschrijving
NCI CTCAE v.3 Grade
Datatype
integer
Alias
- UMLS CUI [1]
- C3887242
Beschrijving
Status
Datatype
integer
Alias
- UMLS CUI [1]
- C0449438
Beschrijving
Classification
Datatype
integer
Alias
- UMLS CUI [1]
- C0008902
Similar models
Screening - Subject Identification; Demography; Disease Characteristics; Status at Screening; Anti-Cancer Therapy; Anti-Cancer Radiotherapy; Medical Conditions
C2986440 (UMLS CUI [1,2])
C0543488 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C0543488 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [1,2])
C0205276 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C0022877 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C0027646 (UMLS CUI [1,2])
C1710477 (UMLS CUI [2])
C0220908 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0279025 (UMLS CUI [2,1])
C0920425 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C1531518 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0332152 (UMLS CUI [3,3])
C0021083 (UMLS CUI [4,1])
C0920425 (UMLS CUI [4,2])
C0332152 (UMLS CUI [4,3])
C0920425 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,3])
C0871468 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])