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ID

14058

Beschrijving

This is an open-label (all people know the identity of the intervention), multicenter study in genotype 1 chronic HCV infected liver transplant patients who will be treated for 12 weeks with telaprevir 750 mg every 8 hours given in combination with Peg-IFN-alfa-2a and ribavirin followed by 36 weeks of treatment with Peg-IFN-alfa-2a and ribavirin alone. The total treatment duration will be 48 weeks. Safety will be evaluated throughout the study and will include evaluations of adverse events, clinical laboratory tests, electrocardiogram, vital signs, and physical examination. NCT01571583

Trefwoorden

  1. 23-03-16 23-03-16 -
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CC BY-NC 3.0

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23 maart 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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    VX-950HPC3006 NCT01571583 Roll Out

    VX-950HPC3006 NCT01571583 Roll Out

    TMC114
    Beschrijving

    TMC114

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5
    TMC125
    Beschrijving

    TMC125

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5
    TMC278
    Beschrijving

    TMC278

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5
    TMC207
    Beschrijving

    TMC207

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5
    VX950
    Beschrijving

    VX950

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5
    TMC 435
    Beschrijving

    TMC 435

    CRF ID
    Beschrijving

    CRF ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    In case subject participates in a non clinial trial please provide date of first dosing
    Beschrijving

    Date of first dose

    Datatype

    date

    Alias
    UMLS CUI [1]
    C3173309 (Date treatment or therapy started)
    LOINC
    LP262646-5

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    VX-950HPC3006 NCT01571583 Roll Out

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    TMC114
    CRF ID
    Item
    CRF ID
    text
    C2348585 (UMLS CUI [1])
    Date of first dose
    Item
    In case subject participates in a non clinial trial please provide date of first dosing
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    In case subject participates in a non clinial trial please provide date of first dosing
    date
    C3173309 (UMLS CUI [1])
    Item Group
    TMC278
    CRF ID
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    CRF ID
    text
    C2348585 (UMLS CUI [1])
    Date of first dose
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    In case subject participates in a non clinial trial please provide date of first dosing
    date
    C3173309 (UMLS CUI [1])
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    TMC207
    CRF ID
    Item
    CRF ID
    text
    C2348585 (UMLS CUI [1])
    Date of first dose
    Item
    In case subject participates in a non clinial trial please provide date of first dosing
    date
    C3173309 (UMLS CUI [1])
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    VX950
    CRF ID
    Item
    CRF ID
    text
    C2348585 (UMLS CUI [1])
    Date of first dose
    Item
    In case subject participates in a non clinial trial please provide date of first dosing
    date
    C3173309 (UMLS CUI [1])
    Item Group
    TMC 435
    CRF ID
    Item
    CRF ID
    text
    C2348585 (UMLS CUI [1])
    Date of first dose
    Item
    In case subject participates in a non clinial trial please provide date of first dosing
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