ID
41999
Descripción
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
Palabras clave
Versiones (3)
- 23/7/18 23/7/18 -
- 18/8/18 18/8/18 -
- 15/3/21 15/3/21 - Dr. rer. medic Philipp Neuhaus
Titular de derechos de autor
GlaxoSmithKline
Subido en
15 de marzo de 2021
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593
Concomitant Medications and Transfusions and Adverse Experiences
- StudyEvent: ODM
Descripción
Concomitant Medications and Transfusions
Alias
- UMLS CUI-1
- C4284232
- UMLS CUI-2
- C0521115
- UMLS CUI-3
- C1879316
- UMLS CUI-4
- C0521115
Descripción
Drug or Blood Product
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013227
- UMLS CUI [2]
- C0456388
Descripción
Drug or Blood Product Dose
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0178602
Descripción
Drug or Blood Product Dose Unit
Tipo de datos
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
Descripción
Route of drug administration
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013153
Descripción
Medication frequency | Transfusion (procedure); Frequencies (time pattern)
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3476109
- UMLS CUI [2,1]
- C1879316
- UMLS CUI [2,2]
- C0439603
Descripción
Date treatment started
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3173309
Descripción
Date treatment stopped
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1531784
Descripción
continuing therapy
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1553904
Descripción
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Descripción
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Descripción
adverse event; Numbers
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0237753
Descripción
Adverse event
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0877248
Descripción
Adverse Event Grade Code
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2985911
Descripción
Serious: Fatal or immediately life- threatening, permanently disabling, requires of prolongs hospitalization, or congenital anomaly.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1519255
Descripción
Adverse Event Onset Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2985916
Descripción
Adverse event; End Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0806020
Descripción
Adverse event; Continuous
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0549178
Descripción
Adverse event; Frequencies (time pattern)
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439603
Descripción
Pharmaceutical Preparations; Therapeutic procedure; Measures
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0079809
Descripción
Record all that apply
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
Descripción
Therapeutic procedure; Measures; Other; Specification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Adverse Event Outcome
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1705586
Descripción
Adverse event; Pharmaceutical Preparations; Relationships
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439849
Descripción
Adverse event; Disease; Relationships
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0439849
Descripción
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])