0 Evaluaciones

ID

31269

Descripción

Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Palabras clave

  1. 6/8/18 6/8/18 -
  2. 18/8/18 18/8/18 -
Titular de derechos de autor

see clinicaltrials.gov

Subido en

6 de agosto de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0

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    Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

    Independent Response Evaluation Oncologist's Assessment and Consensus Criteria

    Response
    Descripción

    Response

    Alias
    UMLS CUI-1
    C0521982
    Date of Response
    Descripción

    Date of Response

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0521982
    UMLS CUI [1,2]
    C0011008
    Response
    Descripción

    Response

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0521982
    Comments
    Descripción

    Comments

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0947611
    Consensus Criteria
    Descripción

    Consensus Criteria

    Alias
    UMLS CUI-1
    C0376298
    UMLS CUI-2
    C0243161
    Response Date (mm/dd/yyyy)
    Descripción

    Response to treatment; Date in time

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0521982
    UMLS CUI [1,2]
    C0011008
    Consensus Response
    Descripción

    Consensus; Response to treatment

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0376298
    UMLS CUI [1,2]
    C0521982
    Comments
    Descripción

    Comments

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0947611
    Administrative
    Descripción

    Administrative

    Alias
    UMLS CUI-1
    C1320722
    Oncologist's Signature
    Descripción

    oncologist; Signature

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0259990
    UMLS CUI [1,2]
    C1519316
    Date of evaluation
    Descripción

    Assessment Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C2985720

    Similar models

    Independent Response Evaluation Oncologist's Assessment and Consensus Criteria

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Response
    C0521982 (UMLS CUI-1)
    Date of Response
    Item
    Date of Response
    date
    C0521982 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Response
    text
    C0521982 (UMLS CUI [1])
    Code List
    Response
    CL Item
    CR (5)
    CL Item
    CCR (4)
    CL Item
    PR (3)
    CL Item
    SD (2)
    CL Item
    PD (1)
    CL Item
    NA / (baseline) (N)
    Comments
    Item
    Comments
    text
    C0947611 (UMLS CUI [1])
    Item Group
    Consensus Criteria
    C0376298 (UMLS CUI-1)
    C0243161 (UMLS CUI-2)
    Response to treatment; Date in time
    Item
    Response Date (mm/dd/yyyy)
    date
    C0521982 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Consensus Response
    text
    C0376298 (UMLS CUI [1,1])
    C0521982 (UMLS CUI [1,2])
    Code List
    Consensus Response
    CL Item
    CR (5)
    CL Item
    CRu (4)
    CL Item
    PR (3)
    CL Item
    SD (2)
    CL Item
    PD (1)
    CL Item
    NA (N)
    Comments
    Item
    Comments
    text
    C0947611 (UMLS CUI [1])
    Item Group
    Administrative
    C1320722 (UMLS CUI-1)
    oncologist; Signature
    Item
    Oncologist's Signature
    text
    C0259990 (UMLS CUI [1,1])
    C1519316 (UMLS CUI [1,2])
    Assessment Date
    Item
    Date of evaluation
    date
    C2985720 (UMLS CUI [1])

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