ID
35310
Descripción
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
Palabras clave
Versiones (1)
- 27/2/19 27/2/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
27 de febrero de 2019
DOI
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Licencia
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
Descripción
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
Descripción
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)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C2826293
- UMLS CUI [1,3]
- C0489540
- UMLS CUI [1,4]
- C2826293
Descripción
Medical and Surgical History
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0489540
Descripción
Seq #
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0237753
Descripción
Description of medical condition or abnormality
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0678257
- UMLS CUI [2,1]
- C1704258
- UMLS CUI [2,2]
- C0678257
Descripción
Year of first diagnosis
Tipo de datos
partialDate
Alias
- UMLS CUI [1,1]
- C0439234
- UMLS CUI [1,2]
- C0011900
Descripción
Ongoing
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0549178
Descripción
Currently being treated with Concomitant Medication?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2347852
Descripción
Disease Stage at Study Entry
Alias
- UMLS CUI-1
- C0699749
- UMLS CUI-2
- C0008976
- UMLS CUI-3
- C1301880
Descripción
Classification of Disease at Study Entry
Alias
- UMLS CUI-1
- C0683326
- UMLS CUI-2
- C0008976
- UMLS CUI-3
- C1301880
Descripción
Did the subject have previous cancer related surgical history?
Alias
- UMLS CUI-1
- C0489540
- UMLS CUI-2
- C2826292
Descripción
Cancer related Surgical History
Alias
- UMLS CUI-1
- C0489540
- UMLS CUI-2
- C2826292
Descripción
Seq #
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0237753
Descripción
Surgery Description (ex. Mastectomy, right breast)
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0678257
- UMLS CUI [2]
- C0024881
Descripción
Surgery Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1628561
Descripción
Previous Anti-Neoplastic Therapy
Alias
- UMLS CUI-1
- C0003392
- UMLS CUI-2
- C1514463
Descripción
If Yes, complete below
Tipo de datos
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
Descripción
Last Previous Anti-Neoplastic Therapy page
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0003392
- UMLS CUI [1,2]
- C1514463
- UMLS CUI [2,1]
- C1704732
- UMLS CUI [2,2]
- C1517741
Descripción
Previous Anti-Neoplastic Therapy
Alias
- UMLS CUI-1
- C0003392
- UMLS CUI-2
- C1514463
Descripción
Seq #
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0237753
Descripción
Type of Therapy
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0087111
Descripción
If other Type of Therapy, please specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Treatment
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0087111
Descripción
Indication
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3146298
Descripción
Date First Dose
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3173309
Descripción
Date Last Dose
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1762893
Descripción
Best Response
Tipo de datos
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])