ID
42022
Descripción
https://clinicaltrials.gov/show/NCT00989664 Patient Withdrawal from Study, Long Term Follow-Up for Survival & Disease Status and Notification of Patient Death Study ID: 104504 Clinical Study ID: BEX104504 Study Title: Multicenter, Pivotal Phase III Study of Iodine-131 Anti-B1 Antibody (Murine) Radioimmunotherapy for Chemotherapy Refractory Low Grade B Cell Lymphomas and Low Grade Lymphomas that have Transformed to Higher Grade Histologies Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00989664 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin
Link
https://clinicaltrials.gov/show/NCT00989664
Palabras clave
Versiones (2)
- 25/5/18 25/5/18 -
- 15/3/21 15/3/21 - Dr. rer. medic Philipp Neuhaus
Titular de derechos de autor
GlaxoSmithKline (GSK)
Subido en
15 de marzo de 2021
DOI
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Licencia
Creative Commons BY-NC 3.0
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Multicenter, Pivotal Phase III Study of Iodine-131 Anti-B1 Antibody (Murine) Radioimmunotherapy NCT00989664
Patient Withdrawal from Study, Long Term Follow-Up for Survival & Disease Status and Notification of Patient Death
Descripción
Long Term Follow-Up for Survival & Disease Status
Alias
- UMLS CUI-1
- C1517942
Descripción
Date of status
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0449437
Descripción
Patient status
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0449437
Descripción
Way of contact
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1705415
- UMLS CUI [1,2]
- C0337611
Descripción
Other way of contact
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1705415
- UMLS CUI [1,2]
- C0337611
Descripción
(If yes, please complete Response Assessment Forms if applicable.)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0768182
- UMLS CUI [1,2]
- C0521982
Descripción
Since the time the last LTFU was completed, has any of the following occured: (If yes, specify below and provide applicable data)
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1706712
Descripción
Myelodysplasia
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0026985
Descripción
(complete both AE & SAE CRFs)
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0026985
Descripción
AML
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0023467
Descripción
(complete both AE & SAE CRFs)
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0023467
Descripción
Other malignancy
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0006826
- UMLS CUI [1,2]
- C0205394
Descripción
(complete both AE & SAE CRFs)
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0006826
- UMLS CUI [1,3]
- C0205394
Descripción
Type of malignancy
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0006826
- UMLS CUI [1,2]
- C0332307
Descripción
Subsequent NHL Therapy since last LTFU
Alias
- UMLS CUI-1
- C2734539
- UMLS CUI-2
- C0008972
Descripción
Subsequent NHL Therapy since last LTFU
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2734539
- UMLS CUI [1,2]
- C0008972
Descripción
Therapy Start date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3173309
Descripción
Therapy Stop Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1531784
Descripción
Total # of Cycles
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0449788
- UMLS CUI [1,2]
- C1302181
Descripción
Laboratory tests
Alias
- UMLS CUI-1
- C0022885
Descripción
TSH Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0040160
- UMLS CUI [1,2]
- C0011008
Descripción
TSH Result
Tipo de datos
float
Unidades de medida
- 𝞵IU/mL
Alias
- UMLS CUI [1,1]
- C0202230
- UMLS CUI [1,2]
- C1274040
Descripción
Thyroid replacement therapy
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2242640
Descripción
Therapy start date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3173309
Descripción
Drug Name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013227
Descripción
HAMA
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1291910
Descripción
Accession #
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1510755
- UMLS CUI [1,2]
- C2826726
Descripción
Administration
Alias
- UMLS CUI-1
- C1320722
Descripción
Notification of death
Alias
- UMLS CUI-1
- C0422202
- UMLS CUI-2
- C0007465
Descripción
If cause of death was related to complications of treatment, please describe or reference forms on which Information is recorded.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0007465
Descripción
Other Cause of Death
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C1521902
Descripción
Relationship of study drug to patient's death
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C0304229
Descripción
Source of Information concerning death of patient
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0030705
- UMLS CUI [1,2]
- C0011065
- UMLS CUI [1,3]
- C0449416
Descripción
Other Source
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0683836
- UMLS CUI [1,2]
- C0011065
- UMLS CUI [1,3]
- C0205394
Similar models
Patient Withdrawal from Study, Long Term Follow-Up for Survival & Disease Status and Notification of Patient Death
C0011008 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0681841 (UMLS CUI [1,2])
C0449437 (UMLS CUI [1,2])
C0337611 (UMLS CUI [1,2])
C0337611 (UMLS CUI [1,2])
C0521982 (UMLS CUI [1,2])
C0026985 (UMLS CUI [1,2])
C0023467 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C0008972 (UMLS CUI-2)
C0008972 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C2826726 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,3])
C0011065 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])