0 Avaliações

ID

42084

Descrição

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 end of study/ end of treatment. Complete this Form when the subject permanently stops the investigational product (IP). If the subject decided to withdraw consent and stop participation in the study, also complete the End of Study Form. If the subject decided to permanently stop the investigational product but will be followed for disease progression or survival per protocol, do not complete the End of Study Form until follow-up is complete.

Link

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

Palavras-chave

  1. 30/03/2021 30/03/2021 -
Titular dos direitos

GlaxoSmithKline

Transferido a

30 de março de 2021

DOI

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Licença

Creative Commons BY-NC 4.0

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    GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

    Investigational product discontinuation

    Administrative Data
    Descrição

    Administrative Data

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

    date of visit/assessment

    Tipo de dados

    date

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

    subject ID

    Tipo de dados

    text

    Alias
    UMLS CUI [1]
    C2348585
    Investigational Product Discontinuation
    Descrição

    Investigational Product Discontinuation

    Alias
    UMLS CUI-1
    C0304229
    UMLS CUI-2
    C0457454
    Give primary reason Investigational Product was permanently stopped
    Descrição

    Select "Adverse event", if the subject has an adverse event due to any cause other than disease progression and the investigational product is permanently stopped due to the adverse event or if the subject died due to any cause other than disease progression. Record details on the Non-Serious Adverse Events or Serious Adverse Events forms as appropriate. Select "investigator discretion" only if the subject permanently stops the IP at the investigator's discretion and none of the other primary reasons apply. Select "Decision by subject or proxy" only if the subject decided to permanently stop the IP and none of the other primary reasons apply.

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0457454
    UMLS CUI [1,3]
    C1549995
    If investigator discretion, please specify:
    Descrição

    Investigational product discontinuation, specification investigator discretion

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0457454
    UMLS CUI [1,3]
    C0008961
    UMLS CUI [1,4]
    C0022423
    If decision by subject or proxy, please specify:
    Descrição

    Investigational product discontinuation, specification decision by subject or proxy

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0457454
    UMLS CUI [1,3]
    C0679006
    UMLS CUI [1,4]
    C0681850
    UMLS CUI [2,1]
    C0304229
    UMLS CUI [2,2]
    C0457454
    UMLS CUI [2,3]
    C0679006
    UMLS CUI [2,4]
    C0600420

    Similar models

    Investigational product discontinuation

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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
    Investigational Product Discontinuation
    C0304229 (UMLS CUI-1)
    C0457454 (UMLS CUI-2)
    Item
    Give primary reason Investigational Product was permanently stopped
    integer
    C0304229 (UMLS CUI [1,1])
    C0457454 (UMLS CUI [1,2])
    C1549995 (UMLS CUI [1,3])
    Code List
    Give primary reason Investigational Product was permanently stopped
    CL Item
    disease progression (including death due to disease progression) (91)
    CL Item
    completed scheduled treatment (92)
    CL Item
    adverse event (1)
    CL Item
    protocol deviation (3)
    CL Item
    study closed/terminated  (5)
    CL Item
    lost to follow-up (6)
    CL Item
    investigator discretion (7)
    CL Item
    Decision by subject or proxy (8)
    Investigational product discontinuation, specification investigator discretion
    Item
    If investigator discretion, please specify:
    text
    C0304229 (UMLS CUI [1,1])
    C0457454 (UMLS CUI [1,2])
    C0008961 (UMLS CUI [1,3])
    C0022423 (UMLS CUI [1,4])
    Investigational product discontinuation, specification decision by subject or proxy
    Item
    If decision by subject or proxy, please specify:
    text
    C0304229 (UMLS CUI [1,1])
    C0457454 (UMLS CUI [1,2])
    C0679006 (UMLS CUI [1,3])
    C0681850 (UMLS CUI [1,4])
    C0304229 (UMLS CUI [2,1])
    C0457454 (UMLS CUI [2,2])
    C0679006 (UMLS CUI [2,3])
    C0600420 (UMLS CUI [2,4])

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