ID
44365
Beschreibung
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
Stichworte
Versionen (4)
- 06.08.18 06.08.18 -
- 06.08.18 06.08.18 -
- 18.08.18 18.08.18 -
- 20.09.21 20.09.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
20. September 2021
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593
Central Pathology Assessment and Description
- StudyEvent: ODM
Beschreibung
Biopsy 2
Alias
- UMLS CUI-1
- C0005558
Beschreibung
Biopsy Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0005558
- UMLS CUI [1,2]
- C0011008
Beschreibung
Biopsy Site
Datentyp
text
Alias
- UMLS CUI [1]
- C1301128
Beschreibung
Accession Number (identifier)
Datentyp
integer
Alias
- UMLS CUI [1]
- C1510755
Beschreibung
Slide (glass microscope); Count
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1705201
- UMLS CUI [1,2]
- C0750480
Beschreibung
Anatomic Site; Original; Name | Anatomic Site; Original; Location
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1515974
- UMLS CUI [1,2]
- C0205313
- UMLS CUI [1,3]
- C0027365
- UMLS CUI [2,1]
- C1515974
- UMLS CUI [2,2]
- C0205313
- UMLS CUI [2,3]
- C0450429
Beschreibung
Working Formulation Classification
Alias
- UMLS CUI-1
- C0024305
- UMLS CUI-2
- C0008902
Beschreibung
Lymphoma, Non-Hodgkin | Classification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0024305
- UMLS CUI [1,2]
- C0008902
Beschreibung
Classification; Other; Specification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0008902
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C2348235
Beschreibung
Histology
Datentyp
text
Alias
- UMLS CUI [1]
- C0019638
Beschreibung
Central Pathologist Assessment
Alias
- UMLS CUI-1
- C1294089
- UMLS CUI-2
- C0205099
Beschreibung
Basis of Assessment
Alias
- UMLS CUI-1
- C0220825
- UMLS CUI-2
- C1874451
Beschreibung
Central Pathologist Assessment Description
Alias
- UMLS CUI-1
- C1294089
- UMLS CUI-2
- C0205099
- UMLS CUI-3
- C0678257
Beschreibung
Description
Datentyp
text
Alias
- UMLS CUI [1]
- C0678257
Beschreibung
Diagnosis; Pathology; Central
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0011900
- UMLS CUI [1,2]
- C0030664
- UMLS CUI [1,3]
- C0205099
Beschreibung
Pathology report; Original; Agreement
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0807321
- UMLS CUI [1,2]
- C0205313
- UMLS CUI [1,3]
- C0680240
Beschreibung
Pathology report; Study Site; Agreement
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0807321
- UMLS CUI [1,2]
- C2825164
- UMLS CUI [1,3]
- C0680240
Beschreibung
Administrative
Alias
- UMLS CUI-1
- C1320722
Ähnliche Modelle
Central Pathology Assessment and Description
- StudyEvent: ODM
C0011008 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C0205313 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
C1515974 (UMLS CUI [2,1])
C0205313 (UMLS CUI [2,2])
C0450429 (UMLS CUI [2,3])
C0011008 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C0205313 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
C1515974 (UMLS CUI [2,1])
C0205313 (UMLS CUI [2,2])
C0450429 (UMLS CUI [2,3])
C0008902 (UMLS CUI-2)
C0008902 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0205099 (UMLS CUI-2)
C0205099 (UMLS CUI [1,2])
C1874451 (UMLS CUI [1,2])
C0205099 (UMLS CUI-2)
C0678257 (UMLS CUI-3)
C0030664 (UMLS CUI [1,2])
C0205099 (UMLS CUI [1,3])
C0205313 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,3])
C2825164 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,3])