ID
35310
Beschrijving
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma
Trefwoorden
Versies (1)
- 27-02-19 27-02-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
27 februari 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556
Screening - Medical and Surgical History; Disease Stage at Study Entry; Classification of Disease at Study Entry; Cancer related Surgical History; Previous Anti-Neoplastic Therapy
Beschrijving
Does the subject have any clinically significant medical or surgical history?
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C2826293
- UMLS CUI-3
- C0489540
- UMLS CUI-4
- C2826293
Beschrijving
If yes, please record details below (please record any new medical conditions occurring after the signing of the Informed Consent Form on the Adverse Events page)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C2826293
- UMLS CUI [1,3]
- C0489540
- UMLS CUI [1,4]
- C2826293
Beschrijving
Medical and Surgical History
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0489540
Beschrijving
Seq #
Datatype
integer
Alias
- UMLS CUI [1]
- C0237753
Beschrijving
Description of medical condition or abnormality
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0678257
- UMLS CUI [2,1]
- C1704258
- UMLS CUI [2,2]
- C0678257
Beschrijving
Year of first diagnosis
Datatype
partialDate
Alias
- UMLS CUI [1,1]
- C0439234
- UMLS CUI [1,2]
- C0011900
Beschrijving
Ongoing
Datatype
boolean
Alias
- UMLS CUI [1]
- C0549178
Beschrijving
Currently being treated with Concomitant Medication?
Datatype
boolean
Alias
- UMLS CUI [1]
- C2347852
Beschrijving
Disease Stage at Study Entry
Alias
- UMLS CUI-1
- C0699749
- UMLS CUI-2
- C0008976
- UMLS CUI-3
- C1301880
Beschrijving
Classification of Disease at Study Entry
Alias
- UMLS CUI-1
- C0683326
- UMLS CUI-2
- C0008976
- UMLS CUI-3
- C1301880
Beschrijving
Did the subject have previous cancer related surgical history?
Alias
- UMLS CUI-1
- C0489540
- UMLS CUI-2
- C2826292
Beschrijving
Cancer related Surgical History
Alias
- UMLS CUI-1
- C0489540
- UMLS CUI-2
- C2826292
Beschrijving
Seq #
Datatype
integer
Alias
- UMLS CUI [1]
- C0237753
Beschrijving
Surgery Description (ex. Mastectomy, right breast)
Datatype
text
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0678257
- UMLS CUI [2]
- C0024881
Beschrijving
Surgery Date
Datatype
date
Alias
- UMLS CUI [1]
- C1628561
Beschrijving
Previous Anti-Neoplastic Therapy
Alias
- UMLS CUI-1
- C0003392
- UMLS CUI-2
- C1514463
Beschrijving
If Yes, complete below
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C1514463
- UMLS CUI [2,1]
- C0279025
- UMLS CUI [2,2]
- C1514463
- UMLS CUI [3,1]
- C0021083
- UMLS CUI [3,2]
- C1514463
- UMLS CUI [4,1]
- C0281176
- UMLS CUI [4,2]
- C1514463
- UMLS CUI [5,1]
- C0017296
- UMLS CUI [5,2]
- C1514463
- UMLS CUI [6,1]
- C1515119
- UMLS CUI [6,2]
- C0026764
- UMLS CUI [6,3]
- C1514463
- UMLS CUI [7,1]
- C1515119
- UMLS CUI [7,2]
- C0006826
- UMLS CUI [7,3]
- C1514463
Beschrijving
Last Previous Anti-Neoplastic Therapy page
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0003392
- UMLS CUI [1,2]
- C1514463
- UMLS CUI [2,1]
- C1704732
- UMLS CUI [2,2]
- C1517741
Beschrijving
Previous Anti-Neoplastic Therapy
Alias
- UMLS CUI-1
- C0003392
- UMLS CUI-2
- C1514463
Beschrijving
Seq #
Datatype
integer
Alias
- UMLS CUI [1]
- C0237753
Beschrijving
Type of Therapy
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0087111
Beschrijving
If other Type of Therapy, please specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschrijving
Treatment
Datatype
text
Alias
- UMLS CUI [1]
- C0087111
Beschrijving
Indication
Datatype
text
Alias
- UMLS CUI [1]
- C3146298
Beschrijving
Date First Dose
Datatype
date
Alias
- UMLS CUI [1]
- C3173309
Beschrijving
Date Last Dose
Datatype
date
Alias
- UMLS CUI [1]
- C1762893
Beschrijving
Best Response
Datatype
integer
Alias
- UMLS CUI [1]
- C2986560
Similar models
Screening - Medical and Surgical History; Disease Stage at Study Entry; Classification of Disease at Study Entry; Cancer related Surgical History; Previous Anti-Neoplastic Therapy
C2826293 (UMLS CUI-2)
C0489540 (UMLS CUI-3)
C2826293 (UMLS CUI-4)
C2826293 (UMLS CUI [1,2])
C0489540 (UMLS CUI [1,3])
C2826293 (UMLS CUI [1,4])
C0489540 (UMLS CUI-2)
C0678257 (UMLS CUI [1,2])
C1704258 (UMLS CUI [2,1])
C0678257 (UMLS CUI [2,2])
C0011900 (UMLS CUI [1,2])
C0008976 (UMLS CUI-2)
C1301880 (UMLS CUI-3)
C0008976 (UMLS CUI-2)
C1301880 (UMLS CUI-3)
C2826292 (UMLS CUI-2)
C2826292 (UMLS CUI [1,2])
C2826292 (UMLS CUI-2)
C0678257 (UMLS CUI [1,2])
C0024881 (UMLS CUI [2])
C1514463 (UMLS CUI-2)
C1514463 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2,1])
C1514463 (UMLS CUI [2,2])
C0021083 (UMLS CUI [3,1])
C1514463 (UMLS CUI [3,2])
C0281176 (UMLS CUI [4,1])
C1514463 (UMLS CUI [4,2])
C0017296 (UMLS CUI [5,1])
C1514463 (UMLS CUI [5,2])
C1515119 (UMLS CUI [6,1])
C0026764 (UMLS CUI [6,2])
C1514463 (UMLS CUI [6,3])
C1515119 (UMLS CUI [7,1])
C0006826 (UMLS CUI [7,2])
C1514463 (UMLS CUI [7,3])
C1514463 (UMLS CUI [1,2])
C1704732 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1514463 (UMLS CUI-2)
C0087111 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])