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ID

41956

Beschreibung

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 observation visits for the cycles of treatment and possible unscheduled visits.

Link

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

Stichworte

  1. 22.02.21 22.02.21 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

22. Februar 2021

DOI

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Lizenz

Creative Commons BY-NC 4.0

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    GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

    New Lymph Node Assessment

    Administrative Data
    Beschreibung

    Administrative Data

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

    date of visit/assessment

    Datentyp

    date

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

    subject ID

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C2348585
    visit type
    Beschreibung

    visit type

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0545082
    UMLS CUI [1,2]
    C0332307
    New Lymph Node Assessment Details
    Beschreibung

    New Lymph Node Assessment Details

    Alias
    UMLS CUI-1
    C0205314
    UMLS CUI-2
    C0024204
    UMLS CUI-3
    C1516048
    UMLS CUI-4
    C1522508
    Lymph node number
    Beschreibung

    [hidden]

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0024204
    UMLS CUI [1,2]
    C0237753
    Lymph node
    Beschreibung

    Lymph node

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0024204
    UMLS CUI [1,2]
    C0450429
    Lymph node location
    Beschreibung

    Lymph node location

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0024204
    UMLS CUI [1,2]
    C0450429
    Method
    Beschreibung

    Lymph node evaluation method

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C2911685
    UMLS CUI [1,2]
    C0024204
    If other, please specify
    Beschreibung

    Other lymph node evaluation method

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0024204
    UMLS CUI [1,2]
    C2911685
    UMLS CUI [1,3]
    C0205394
    Date
    Beschreibung

    Lymph node, date of assessment

    Datentyp

    date

    Alias
    UMLS CUI [1,1]
    C0024204
    UMLS CUI [1,2]
    C2985720
    Longest diameter
    Beschreibung

    Lymph node, longest diameter

    Datentyp

    integer

    Maßeinheiten
    • cm
    Alias
    UMLS CUI [1,1]
    C1301886
    UMLS CUI [1,2]
    C1522425
    UMLS CUI [1,3]
    C0024204
    cm
    Shortest diameter
    Beschreibung

    Lymph node, shortest diameter

    Datentyp

    integer

    Maßeinheiten
    • cm
    Alias
    UMLS CUI [1,1]
    C1301886
    UMLS CUI [1,2]
    C1806781
    UMLS CUI [1,3]
    C0024204
    cm

    Ähnliche Modelle

    New Lymph Node Assessment

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    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
    integer
    C0545082 (UMLS CUI [1,1])
    C0332307 (UMLS CUI [1,2])
    Code List
    visit type
    CL Item
    Cycle 1 Observation visit (1)
    CL Item
    Cycle 2 Observation visit (2)
    CL Item
    Unscheduled visit (3)
    Item Group
    New Lymph Node Assessment Details
    C0205314 (UMLS CUI-1)
    C0024204 (UMLS CUI-2)
    C1516048 (UMLS CUI-3)
    C1522508 (UMLS CUI-4)
    Lymph node number
    Item
    Lymph node number
    text
    C0024204 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Item
    Lymph node
    text
    C0024204 (UMLS CUI [1,1])
    C0450429 (UMLS CUI [1,2])
    Code List
    Lymph node
    CL Item
    cervical right (1)
    CL Item
    femoral right (10)
    CL Item
    celiac (11)
    CL Item
    hilar left (12)
    CL Item
    hilar right (13)
    CL Item
    iliac-common (14)
    CL Item
    iliac-internal (15)
    CL Item
    iliac-external (16)
    CL Item
    infraclavicular left (17)
    CL Item
    infraclavicular right (18)
    CL Item
    mediastinal (19)
    CL Item
    cervical left (2)
    CL Item
    paraaortic (21)
    CL Item
    parapharyngeal  (22)
    CL Item
    paratracheal (23)
    CL Item
    periportal (24)
    CL Item
    portal (25)
    CL Item
    retrocrural (26)
    CL Item
    retroperitoneal (27)
    CL Item
    splenic (hepatic) hilar (28)
    CL Item
    supraclavicular right (3)
    CL Item
    supraclavicular left  (4)
    CL Item
    axillary left (5)
    CL Item
    axillary right (6)
    CL Item
    inguinal left (7)
    CL Item
    inguinal right (8)
    CL Item
    femoral left (9)
    CL Item
    other (OT)
    Lymph node location
    Item
    Lymph node location
    text
    C0024204 (UMLS CUI [1,1])
    C0450429 (UMLS CUI [1,2])
    Item
    Method
    text
    C2911685 (UMLS CUI [1,1])
    C0024204 (UMLS CUI [1,2])
    CL Item
    Conventional CT scan (C)
    CL Item
    Direct measure by physical exam  (D)
    CL Item
    Endoscopy (E)
    CL Item
    High-resolution CT scan (HC)
    CL Item
    Lymphangiogram (L)
    CL Item
    MRI (M)
    CL Item
    Mammography (MA)
    CL Item
    Nuclear scan (NS)
    CL Item
    Medical photography (P)
    CL Item
    PET/CT scan (PC)
    CL Item
    Panendoscopy (PE)
    CL Item
    Spiral CT scan (SC)
    CL Item
    X-ray (XR)
    CL Item
    Total body X-ray (TX)
    CL Item
    Ultrasound (UL)
    CL Item
    Other (OT)
    Other lymph node evaluation method
    Item
    If other, please specify
    text
    C0024204 (UMLS CUI [1,1])
    C2911685 (UMLS CUI [1,2])
    C0205394 (UMLS CUI [1,3])
    Lymph node, date of assessment
    Item
    Date
    date
    C0024204 (UMLS CUI [1,1])
    C2985720 (UMLS CUI [1,2])
    Lymph node, longest diameter
    Item
    Longest diameter
    integer
    C1301886 (UMLS CUI [1,1])
    C1522425 (UMLS CUI [1,2])
    C0024204 (UMLS CUI [1,3])
    Lymph node, shortest diameter
    Item
    Shortest diameter
    integer
    C1301886 (UMLS CUI [1,1])
    C1806781 (UMLS CUI [1,2])
    C0024204 (UMLS CUI [1,3])

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