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ID

41889

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 has to be filled out at the screening visit, the weekly visits during the cycles of treatment, the cycle observation visits, unscheduled visits, withdrawal visits and visits at the end of study/ treatment.

Link

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

Keywords

  1. 2/9/21 2/9/21 -
Copyright Holder

GlaxoSmithKline

Uploaded on

February 9, 2021

DOI

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License

Creative Commons BY-NC 4.0

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    GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

    Constitutional Symptoms and ECOG

    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    date of visit/assessment
    Description

    date of visit/assessment

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303 (Date of visit)
    SNOMED
    406543005
    UMLS CUI [2]
    C2985720 (Assessment Date)
    subject number
    Description

    subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    visit type
    Description

    visit type

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0545082 (Visit)
    UMLS CUI [1,2]
    C0332307 (Type - attribute)
    SNOMED
    261664005
    Constitutional Symptoms
    Description

    Constitutional Symptoms

    Alias
    UMLS CUI-1
    C0009812 (Constitutional Symptom)
    Night sweats without signs of infection
    Description

    Night sweats without signs of infection

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0028081 (Night sweats)
    SNOMED
    42984000
    LOINC
    LP75171-6
    UMLS CUI [1,2]
    C0009450 (Communicable Diseases)
    SNOMED
    189822004
    UMLS CUI [1,3]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    Unintentional weight loss >= 10% within the previous 6 months
    Description

    Recent unintentional weight loss

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0332185 (Recent)
    SNOMED
    6493001
    UMLS CUI [1,2]
    C2363736 (Unintentional weight loss)
    SNOMED
    448765001
    Recurrent, unexplained fever of greater than 100°F for 2 weeks without signs of infection
    Description

    Recurrent, unexplained fever

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C2945760 (Recurrent)
    SNOMED
    255227004
    UMLS CUI [1,2]
    C1844662 (Unexplained fevers)
    Extreme fatigue
    Description

    Extreme fatigue

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0205403 (Extreme)
    SNOMED
    12565001
    LOINC
    LA14868-6
    UMLS CUI [1,2]
    C0015672 (Fatigue)
    SNOMED
    248274002
    LOINC
    MTHU013358
    ECOG Performance Status Scale
    Description

    ECOG Performance Status Scale

    Alias
    UMLS CUI-1
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    Total Score
    Description

    ECOG Performance status, total score

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    UMLS CUI [1,2]
    C2964552 (Total score)
    LOINC
    LP101867-2

    Similar models

    Constitutional Symptoms and ECOG

    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
    visit type
    text
    C0545082 (UMLS CUI [1,1])
    C0332307 (UMLS CUI [1,2])
    Code List
    visit type
    CL Item
    Screening visit (A)
    CL Item
    Cycle 1 week 1 (B)
    CL Item
    Cycle 1 week 2 (C)
    CL Item
    Cycle 1 week 3  (D)
    CL Item
    Cycle 1 week 4 (E)
    CL Item
    Cycle 1 Observation  (F)
    CL Item
    unscheduled visit (G)
    CL Item
    Withdrawal visit (H)
    CL Item
    End of Study / Treatment (I)
    CL Item
    Cycle 2 Week 1 (J)
    CL Item
    Cycle 2 Week 2 (K)
    CL Item
    Cycle 2 Week 3 (L)
    CL Item
    Cycle 2 Week 4 (M)
    CL Item
    Cycle 2 Observation (N)
    Item Group
    Constitutional Symptoms
    C0009812 (UMLS CUI-1)
    Night sweats without signs of infection
    Item
    Night sweats without signs of infection
    boolean
    C0028081 (UMLS CUI [1,1])
    C0009450 (UMLS CUI [1,2])
    C0332197 (UMLS CUI [1,3])
    Recent unintentional weight loss
    Item
    Unintentional weight loss >= 10% within the previous 6 months
    boolean
    C0332185 (UMLS CUI [1,1])
    C2363736 (UMLS CUI [1,2])
    Recurrent, unexplained fever
    Item
    Recurrent, unexplained fever of greater than 100°F for 2 weeks without signs of infection
    boolean
    C2945760 (UMLS CUI [1,1])
    C1844662 (UMLS CUI [1,2])
    Extreme fatigue
    Item
    Extreme fatigue
    boolean
    C0205403 (UMLS CUI [1,1])
    C0015672 (UMLS CUI [1,2])
    Item Group
    ECOG Performance Status Scale
    C1520224 (UMLS CUI-1)
    ECOG Performance status, total score
    Item
    Total Score
    text
    C1520224 (UMLS CUI [1,1])
    C2964552 (UMLS CUI [1,2])

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