ID

31372

Description

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

Keywords

Versions (3)
  1. 7/23/18 7/23/18 -
  2. 8/18/18 8/18/18 -
  3. 3/15/21 3/15/21 - Dr. rer. medic Philipp Neuhaus
Copyright Holder

GlaxoSmithKline

Uploaded on

August 18, 2018

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

English

Concomitant Medications and Transfusions and Adverse Experiences

1 forms  
Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Series Page
Description

Series Page

Data type

text

Alias
UMLS CUI [1,1]
C0205549
UMLS CUI [1,2]
C1704732
Last Page
Description

Last Page

Data type

boolean

Alias
UMLS CUI [1,1]
C1704732
UMLS CUI [1,2]
C1517741
Concomitant Medications and Transfusions
Description

Concomitant Medications and Transfusions

Alias
UMLS CUI-1
C4284232
UMLS CUI-2
C0521115
UMLS CUI-3
C1879316
UMLS CUI-4
C0521115
Drug or Blood Product
Description

Drug or Blood Product

Data type

text

Alias
UMLS CUI [1]
C0013227
UMLS CUI [2]
C0456388
Drug or Blood Product Dose
Description

Drug or Blood Product Dose

Data type

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0456388
UMLS CUI [2,2]
C0178602
Drug or Blood Product Dose Unit
Description

Drug or Blood Product Dose Unit

Data type

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
Route of drug administration
Description

Route of drug administration

Data type

text

Alias
UMLS CUI [1]
C0013153
Medication and Transfusion frequency
Description

Medication frequency | Transfusion (procedure); Frequencies (time pattern)

Data type

text

Alias
UMLS CUI [1]
C3476109
UMLS CUI [2,1]
C1879316
UMLS CUI [2,2]
C0439603
Treatment Start Date (mm/dd/yy)
Description

Date treatment started

Data type

date

Alias
UMLS CUI [1]
C1531783
Treatment Stop Date (mm/dd/yy)
Description

Date treatment stopped

Data type

date

Alias
UMLS CUI [1]
C1531784
If treatment is continuing, please check
Description

continuing therapy

Data type

text

Alias
UMLS CUI [1]
C1553904
Back to the top of the page

Similar models

Concomitant Medications and Transfusions and Adverse Experiences

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Series Page
Item
Series Page
text
C0205549 (UMLS CUI [1,1])
C1704732 (UMLS CUI [1,2])
Last Page
Item
Last Page
boolean
C1704732 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
Item Group
Concomitant Medications and Transfusions
C4284232 (UMLS CUI-1)
C0521115 (UMLS CUI-2)
C1879316 (UMLS CUI-3)
C0521115 (UMLS CUI-4)
Drug or Blood Product
Item
Drug or Blood Product
text
C0013227 (UMLS CUI [1])
C0456388 (UMLS CUI [2])
Drug or Blood Product Dose
Item
Drug or Blood Product Dose
text
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Drug or Blood Product Dose Unit
Item
Drug or Blood Product Dose Unit
text
C0013227 (UMLS CUI [1,1])
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])
Route of drug administration
Item
Route of drug administration
text
C0013153 (UMLS CUI [1])
Medication frequency | Transfusion (procedure); Frequencies (time pattern)
Item
Medication and Transfusion frequency
text
C3476109 (UMLS CUI [1])
C1879316 (UMLS CUI [2,1])
C0439603 (UMLS CUI [2,2])
Date treatment started
Item
Treatment Start Date (mm/dd/yy)
date
C1531783 (UMLS CUI [1])
Date treatment stopped
Item
Treatment Stop Date (mm/dd/yy)
date
C1531784 (UMLS CUI [1])
Item
If treatment is continuing, please check
text
C1553904 (UMLS CUI [1])
continuing therapy
Code List
If treatment is continuing, please check
CL Item
continuing therapy (C)
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial