ID

31183

Description

Study ID: 104505 Clinical Study ID: BEX104505 Study Title: Phase II Study of Iodine 131 Anti B1 Antibody for 1st or 2nd Relapsed Indolent B-Cell Lymphomas or B-Cell Lymphomas That Have Transformed to a More Aggressive Histology Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00950755 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin Please record all concomitant medications and transfusions from the time of study entry through the Week 13 visit. Include study-required medications (i.e. Lugol's solution or potassium iodide, paracetamol, and diphenhydramine).

Keywords

Versions (1)
  1. 7/25/18 7/25/18 -
Copyright Holder

see clinicaltrials.gov

Uploaded on

July 25, 2018

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License

Creative Commons BY 4.0
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Iodine 131 B1 Antibody for B-Cell Lymphomas NCT00950755

English

Concomitant Medications & Transfusions

1 forms  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Site Number
Description

Site number

Data type

text

Alias
UMLS CUI [1,1]
C0018704
UMLS CUI [1,2]
C0600091
Patient Number
Description

Patient Number

Data type

text

Alias
UMLS CUI [1]
C1830427
Patient Initials
Description

Patient Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Concomitant Medications; Concomitant Transfusions
Description

Concomitant Medications; Concomitant Transfusions

Alias
UMLS CUI-1
C2347852
Drug Name or Blood Product
Description

Concomitant Agent; Drug Name or Blood Product

Data type

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C2360065
UMLS CUI [1,3]
C0456388
Dose
Description

Concomitant Agent; Dose

Data type

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C3174092
Unit
Description

Concomitant Agent; Unit

Data type

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C1519795
Route
Description

Concomitant Agent; Route

Data type

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0013153
Frequency
Description

Concomitant Agent; Frequency

Data type

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C3476109
Start Date
Description

Concomitant Agent; Start Date

Data type

date

Alias
UMLS CUI [1]
C2826734
End Date
Description

Concomitant Agent; End Date

Data type

date

Alias
UMLS CUI [1]
C2826744
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Similar models

Concomitant Medications & Transfusions

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Site number
Item
Site Number
text
C0018704 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item Group
Concomitant Medications; Concomitant Transfusions
C2347852 (UMLS CUI-1)
Concomitant Agent; Drug Name or Blood Product
Item
Drug Name or Blood Product
text
C2347852 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C0456388 (UMLS CUI [1,3])
Concomitant Agent; Dose
Item
Dose
text
C2347852 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
Concomitant Agent; Unit
Item
Unit
text
C2347852 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Concomitant Agent; Route
Item
Route
text
C2347852 (UMLS CUI [1,1])
C0013153 (UMLS CUI [1,2])
Concomitant Agent; Frequency
Item
Frequency
text
C2347852 (UMLS CUI [1,1])
C3476109 (UMLS CUI [1,2])
Concomitant Agent; Start Date
Item
Start Date
date
C2826734 (UMLS CUI [1])
Concomitant Agent; End Date
Item
End Date
date
C2826744 (UMLS CUI [1])
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