ID
35567
Description
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
Mots-clés
Versions (1)
- 10/03/2019 10/03/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
10 mars 2019
DOI
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Licence
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
SRT501 + Bortezomib Cycle __ Day 8 (Post Dose) - Vital Signs; SRT501 Administration; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment
Description
Vital Signs
Alias
- UMLS CUI-1
- C0518766
Description
If Yes, complete below
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C1516048
Description
Date of assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
Check one box only
Type de données
integer
Alias
- UMLS CUI [1]
- C1262869
Description
Systolic BP
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Diastolic BP
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Heart Rate
Type de données
integer
Unités de mesure
- beats/min
Alias
- UMLS CUI [1]
- C0018810
Description
Respiration Rate
Type de données
integer
Unités de mesure
- breaths/min
Alias
- UMLS CUI [1]
- C0231832
Description
Temperature
Type de données
float
Alias
- UMLS CUI [1]
- C0005903
Description
Check one box only
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C1519795
Description
Weight
Type de données
float
Alias
- UMLS CUI [1]
- C0005910
Description
Check one box only
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C0439148
Description
SRT501 Administration
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1320722
Description
Was SRT501 administered at this visit?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1320722
Description
Date administered
Type de données
date
Alias
- UMLS CUI [1,1]
- C1521801
- UMLS CUI [1,2]
- C0011008
Description
Kit #
Type de données
integer
Alias
- UMLS CUI [1]
- C2981406
Description
Time Administered
Type de données
time
Alias
- UMLS CUI [1,1]
- C1521801
- UMLS CUI [1,2]
- C0040223
Description
Study Treatment Compliance (Return)
Alias
- UMLS CUI-1
- C1321605
- UMLS CUI-2
- C0332156
Description
If No, please complete the comments page or the protocol deviations page.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C3890583
- UMLS CUI [1,2]
- C0332156
Description
If No, please complete the comments page or the protocol deviations page. If No, please provide the number of missed doses and the dates that the doses were missed
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0178602
Description
No. of missed dates:
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1705492
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0237753
Description
Dates dose missed:
Type de données
text
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1705492
- UMLS CUI [1,3]
- C0178602
Description
New Adverse Events and Concomitant Treatment
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2347852
Description
If Yes, please record details on Adverse Events page.
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
If Yes, please record details on Concomitant Treatment page.
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2,1]
- C0678766
- UMLS CUI [2,2]
- C0205217
- UMLS CUI [3,1]
- C0678766
- UMLS CUI [3,2]
- C0205216
- UMLS CUI [4,1]
- C0439603
- UMLS CUI [4,2]
- C0205217
- UMLS CUI [5,1]
- C0439603
- UMLS CUI [5,2]
- C0205216
Similar models
SRT501 + Bortezomib Cycle __ Day 8 (Post Dose) - Vital Signs; SRT501 Administration; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment
C1516048 (UMLS CUI [1,2])
C1320722 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0332156 (UMLS CUI-2)
C0332156 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C1705492 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C2347852 (UMLS CUI-2)
C0678766 (UMLS CUI [2,1])
C0205217 (UMLS CUI [2,2])
C0678766 (UMLS CUI [3,1])
C0205216 (UMLS CUI [3,2])
C0439603 (UMLS CUI [4,1])
C0205217 (UMLS CUI [4,2])
C0439603 (UMLS CUI [5,1])
C0205216 (UMLS CUI [5,2])