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ID

31178

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

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Versions (1)
  1. 7/25/18 7/25/18 -
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see clinicaltrials.gov

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July 25, 2018

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

    English

    Patient Withdrawal from Study

    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
    Date of withdrawal from study
    Description

    Withdrawal Date

    Data type

    date

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

    Withdrawal from study

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

    Withdrawal from study; reason

    Data type

    text

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

    Withdrawal from study, explanation

    Data type

    text

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

    Patient Withdrawal from Study

    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])
    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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