ID

31178

Beschrijving

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

Trefwoorden

Versies (1)
  1. 25-07-18 25-07-18 -
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see clinicaltrials.gov

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25 juli 2018

DOI

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Licentie

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

Engels

Patient Withdrawal from Study

1 Formulieren  
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Site Number
Beschrijving

Site number

Datatype

text

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

Patient Number

Datatype

text

Alias
UMLS CUI [1]
C1830427
Patient Initials
Beschrijving

Patient Initials

Datatype

text

Alias
UMLS CUI [1]
C2986440
Date of withdrawal from study
Beschrijving

Withdrawal Date

Datatype

date

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0011008
Withdrawal from study
Beschrijving

Withdrawal from study

Alias
UMLS CUI-1
C0422727
Reason for withdrawal from study (check primary reason only)
Beschrijving

Withdrawal from study; reason

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0085978
Explanation of withdrawal
Beschrijving

Withdrawal from study, explanation

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0681841
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Similar models

Patient Withdrawal from Study

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Withdrawal Date
Item
Date of withdrawal from study
date
C2349954 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Withdrawal from study
C0422727 (UMLS CUI-1)
Item
Reason for withdrawal from study (check primary reason only)
text
C0422727 (UMLS CUI [1,1])
C0085978 (UMLS CUI [1,2])
Withdrawal from study; reason
Code List
Reason for withdrawal from study (check primary reason only)
CL Item
Patient was lost to follow up (Date of last contact and explain below). (Patient was lost to follow up (Date of last contact and explain below).)
CL Item
Patient wished to withdraw from study (explain below). (Patient wished to withdraw from study (explain below).)
CL Item
Patient received an alternate therapy (explain below). (Patient received an alternate therapy (explain below).)
CL Item
Patient had progressive disease. (Patient had progressive disease.)
CL Item
Patient died. (Patient died.)
CL Item
Other (specify) (Other (specify))
Withdrawal from study, explanation
Item
Explanation of withdrawal
text
C0422727 (UMLS CUI [1,1])
C0681841 (UMLS CUI [1,2])
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