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ID

32391

Beschrijving

Safety and Efficacy of GMX1777 in the Treatment of Refractory Solid Tumors or Lymphomas; ODM derived from: https://clinicaltrials.gov/show/NCT00457574

Link

https://clinicaltrials.gov/show/NCT00457574

Trefwoorden

Versies (1)
  1. 29-10-18 29-10-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

29 oktober 2018

DOI

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Licentie

Creative Commons BY 4.0
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    Eligibility Solid Tumors and Lymphomas NCT00457574

    Engels

    Eligibility Solid Tumors and Lymphomas NCT00457574

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients must have a histologically or cytologically confirmed solid tumor or lymphoma
    Beschrijving

    Solid Neoplasm | Lymphoma

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0280100
    UMLS CUI [2]
    C0024299
    no limitations on allowable type and amount of prior therapy.
    Beschrijving

    Limitation Absent Prior Therapy

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0449295
    UMLS CUI [1,2]
    C0332197
    UMLS CUI [1,3]
    C1514463
    patients must have a life expectancy of greater than 8 weeks
    Beschrijving

    Life Expectancy

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0023671
    patients must have normal organ and marrow function
    Beschrijving

    Organ function | Bone Marrow function

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0678852
    UMLS CUI [2,1]
    C0005953
    UMLS CUI [2,2]
    C0031843
    patients must be willing to submit blood sampling for planned pk analysis
    Beschrijving

    Blood sampling Pharmacokinetic aspects

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0005834
    UMLS CUI [1,2]
    C0031328
    patients must have the ability to understand and willingness to sign a written informed consent form
    Beschrijving

    Informed Consent

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    no other agents or therapies administered with the intent to treat malignancy
    Beschrijving

    Pharmaceutical Preparations Other Cancer treatment | Cancer treatment Other

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0205394
    UMLS CUI [1,3]
    C0920425
    UMLS CUI [2,1]
    C0920425
    UMLS CUI [2,2]
    C0205394
    patients with prior exposure to gmx1777 or gmx1778
    Beschrijving

    Exposure to GMX1777 | Exposure to GMX 1778

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0332157
    UMLS CUI [1,2]
    C2346839
    UMLS CUI [2,1]
    C0332157
    UMLS CUI [2,2]
    C2713488
    uncontrolled, intercurrent illness
    Beschrijving

    Comorbidity Uncontrolled

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0009488
    UMLS CUI [1,2]
    C0205318
    pregnant women and women who are breast feeding
    Beschrijving

    Pregnancy | Breast Feeding

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    Terug naar het begin van de pagina

    Similar models

    Eligibility Solid Tumors and Lymphomas NCT00457574

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Solid Neoplasm | Lymphoma
    Item
    patients must have a histologically or cytologically confirmed solid tumor or lymphoma
    boolean
    C0280100 (UMLS CUI [1])
    C0024299 (UMLS CUI [2])
    Limitation Absent Prior Therapy
    Item
    no limitations on allowable type and amount of prior therapy.
    boolean
    C0449295 (UMLS CUI [1,1])
    C0332197 (UMLS CUI [1,2])
    C1514463 (UMLS CUI [1,3])
    Life Expectancy
    Item
    patients must have a life expectancy of greater than 8 weeks
    boolean
    C0023671 (UMLS CUI [1])
    Organ function | Bone Marrow function
    Item
    patients must have normal organ and marrow function
    boolean
    C0678852 (UMLS CUI [1])
    C0005953 (UMLS CUI [2,1])
    C0031843 (UMLS CUI [2,2])
    Blood sampling Pharmacokinetic aspects
    Item
    patients must be willing to submit blood sampling for planned pk analysis
    boolean
    C0005834 (UMLS CUI [1,1])
    C0031328 (UMLS CUI [1,2])
    Informed Consent
    Item
    patients must have the ability to understand and willingness to sign a written informed consent form
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Pharmaceutical Preparations Other Cancer treatment | Cancer treatment Other
    Item
    no other agents or therapies administered with the intent to treat malignancy
    boolean
    C0013227 (UMLS CUI [1,1])
    C0205394 (UMLS CUI [1,2])
    C0920425 (UMLS CUI [1,3])
    C0920425 (UMLS CUI [2,1])
    C0205394 (UMLS CUI [2,2])
    Exposure to GMX1777 | Exposure to GMX 1778
    Item
    patients with prior exposure to gmx1777 or gmx1778
    boolean
    C0332157 (UMLS CUI [1,1])
    C2346839 (UMLS CUI [1,2])
    C0332157 (UMLS CUI [2,1])
    C2713488 (UMLS CUI [2,2])
    Comorbidity Uncontrolled
    Item
    uncontrolled, intercurrent illness
    boolean
    C0009488 (UMLS CUI [1,1])
    C0205318 (UMLS CUI [1,2])
    Pregnancy | Breast Feeding
    Item
    pregnant women and women who are breast feeding
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Terug naar het begin van de pagina 

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