ID
41999
Beschrijving
Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin
Trefwoorden
Versies (3)
- 23-07-18 23-07-18 -
- 18-08-18 18-08-18 -
- 15-03-21 15-03-21 - Dr. rer. medic Philipp Neuhaus
Houder van rechten
GlaxoSmithKline
Geüploaded op
15 maart 2021
DOI
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Licentie
Creative Commons BY-NC 3.0
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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593
Concomitant Medications and Transfusions and Adverse Experiences
- StudyEvent: ODM
Beschrijving
Concomitant Medications and Transfusions
Alias
- UMLS CUI-1
- C4284232
- UMLS CUI-2
- C0521115
- UMLS CUI-3
- C1879316
- UMLS CUI-4
- C0521115
Beschrijving
Drug or Blood Product
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
- UMLS CUI [2]
- C0456388
Beschrijving
Drug or Blood Product Dose
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0178602
Beschrijving
Drug or Blood Product Dose Unit
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C0439148
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0178602
- UMLS CUI [2,3]
- C0439148
Beschrijving
Route of drug administration
Datatype
text
Alias
- UMLS CUI [1]
- C0013153
Beschrijving
Medication frequency | Transfusion (procedure); Frequencies (time pattern)
Datatype
text
Alias
- UMLS CUI [1]
- C3476109
- UMLS CUI [2,1]
- C1879316
- UMLS CUI [2,2]
- C0439603
Beschrijving
Date treatment started
Datatype
date
Alias
- UMLS CUI [1]
- C3173309
Beschrijving
Date treatment stopped
Datatype
date
Alias
- UMLS CUI [1]
- C1531784
Beschrijving
continuing therapy
Datatype
text
Alias
- UMLS CUI [1]
- C1553904
Beschrijving
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Beschrijving
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Beschrijving
adverse event; Numbers
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0237753
Beschrijving
Adverse event
Datatype
text
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
Adverse Event Grade Code
Datatype
text
Alias
- UMLS CUI [1]
- C2985911
Beschrijving
Serious: Fatal or immediately life- threatening, permanently disabling, requires of prolongs hospitalization, or congenital anomaly.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
Adverse Event Onset Date
Datatype
date
Alias
- UMLS CUI [1]
- C2985916
Beschrijving
Adverse event; End Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0806020
Beschrijving
Adverse event; Continuous
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0549178
Beschrijving
Adverse event; Frequencies (time pattern)
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439603
Beschrijving
Pharmaceutical Preparations; Therapeutic procedure; Measures
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0079809
Beschrijving
Record all that apply
Datatype
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
Beschrijving
Therapeutic procedure; Measures; Other; Specification
Datatype
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beschrijving
Adverse Event Outcome
Datatype
text
Alias
- UMLS CUI [1]
- C1705586
Beschrijving
Adverse event; Pharmaceutical Preparations; Relationships
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439849
Beschrijving
Adverse event; Disease; Relationships
Datatype
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0439849
Beschrijving
Investigator Signature
Alias
- UMLS CUI-1
- C2346576
Similar models
Concomitant Medications and Transfusions and Adverse Experiences
- StudyEvent: ODM
C1704732 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,2])
C0521115 (UMLS CUI-2)
C1879316 (UMLS CUI-3)
C0521115 (UMLS CUI-4)
C0456388 (UMLS CUI [2])
C0178602 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0178602 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C0456388 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0439148 (UMLS CUI [2,3])
C1879316 (UMLS CUI [2,1])
C0439603 (UMLS CUI [2,2])
C0237753 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0079809 (UMLS CUI [1,3])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0013227 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])