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ID

42085

Description

Study ID: 110921 Clinical Study ID: 110921 Study Title: A Phase II Trial of Ofatumumab in Subjects with Waldenstrom's Macroglobulinemia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00811733 Clinicaltrials.gov Link: https://clinicaltrials.gov/ct2/show/NCT00811733 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Ofatumumab Trade Name: N/A Study Indication: Waldenstrom Macroglobulinaemia The primary objective of this open-label, multi-center, Phase II study was to evaluate the safety and efficacy of Ofatumumab in subjects diagnosed with Waldenstrom Macroglobulinaemia. For the study, eligible subjects were enrolled to receive up to 3 cycles of treatment with Ofatumumab. The first cycle consisted of a single dose of 300 mg followed by 3 weekly doses of 1000 mg (Treatment Group A) or 4 weekly doses of 2000 mg (Treatment Group B) of Ofatumumab, with response assessment beginning at Week 12. Based on the Week 12-16 response, eligible subjects could receive up to 2 additional cycles of treatment. This form is for logging, if any concomitant medication, (non-)serious adverse events, blood (supportive care) products or additional scans occurred during the study.

Link

https://clinicaltrials.gov/ct2/show/NCT00811733

Keywords

  1. 3/30/21 3/30/21 -
  2. 4/7/21 4/7/21 -
Copyright Holder

GlaxoSmithKline

Uploaded on

March 30, 2021

DOI

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License

Creative Commons BY-NC 4.0

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    GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

    Log Status

    1. StudyEvent: ODM
      1. Log Status
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    date of visit/assessment
    Description

    date of visit/assessment

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303
    UMLS CUI [2]
    C2985720
    subject number
    Description

    subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Log Status
    Description

    Log Status

    Alias
    UMLS CUI-1
    C1708728
    UMLS CUI-2
    C0449438
    Were any concomitant medications taken by the subject prior to screening and/or during the study?
    Description

    Concomitant medication taken prior to screening and/or during study

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0332152
    UMLS CUI [1,3]
    C0220908
    UMLS CUI [2,1]
    C2347852
    UMLS CUI [2,2]
    C0347984
    UMLS CUI [2,3]
    C2347804
    Did the subject experience any non-serious adverse events during the study?
    Description

    Non-serious adverse events during study

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1518404
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C2347804
    Did the subject experience a serious adverse event during the study?
    Description

    Serious adverse event during study

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1519255
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C2347804
    Were any blood products / blood supportive care products taken by the subject during the study?
    Description

    Blood products / blood supportive care products taken during study

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0456388
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C2347804
    UMLS CUI [2,1]
    C0018938
    UMLS CUI [2,2]
    C0347984
    UMLS CUI [2,3]
    C2347804
    Were any other/additional scans performed
    Description

    Other/additional scans performed

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C0011923
    UMLS CUI [2,1]
    C1524062
    UMLS CUI [2,2]
    C0011923

    Similar models

    Log Status

    1. StudyEvent: ODM
      1. Log Status
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    date of visit/assessment
    Item
    date of visit/assessment
    date
    C1320303 (UMLS CUI [1])
    C2985720 (UMLS CUI [2])
    subject ID
    Item
    subject number
    text
    C2348585 (UMLS CUI [1])
    Item Group
    Log Status
    C1708728 (UMLS CUI-1)
    C0449438 (UMLS CUI-2)
    Item
    Were any concomitant medications taken by the subject prior to screening and/or during the study?
    text
    C2347852 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    C0220908 (UMLS CUI [1,3])
    C2347852 (UMLS CUI [2,1])
    C0347984 (UMLS CUI [2,2])
    C2347804 (UMLS CUI [2,3])
    Code List
    Were any concomitant medications taken by the subject prior to screening and/or during the study?
    CL Item
    yes (y)
    CL Item
    no (n)
    Item
    Did the subject experience any non-serious adverse events during the study?
    text
    C1518404 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C2347804 (UMLS CUI [1,3])
    Code List
    Did the subject experience any non-serious adverse events during the study?
    CL Item
    yes (y)
    CL Item
    no (n)
    Item
    Did the subject experience a serious adverse event during the study?
    text
    C1519255 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C2347804 (UMLS CUI [1,3])
    Code List
    Did the subject experience a serious adverse event during the study?
    CL Item
    yes (y)
    CL Item
    no (n)
    Item
    Were any blood products / blood supportive care products taken by the subject during the study?
    text
    C0456388 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C2347804 (UMLS CUI [1,3])
    C0018938 (UMLS CUI [2,1])
    C0347984 (UMLS CUI [2,2])
    C2347804 (UMLS CUI [2,3])
    Code List
    Were any blood products / blood supportive care products taken by the subject during the study?
    CL Item
    yes (y)
    CL Item
    no (n)
    Item
    Were any other/additional scans performed
    text
    C0205394 (UMLS CUI [1,1])
    C0011923 (UMLS CUI [1,2])
    C1524062 (UMLS CUI [2,1])
    C0011923 (UMLS CUI [2,2])
    Code List
    Were any other/additional scans performed
    CL Item
    yes (y)
    CL Item
    no (n)

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