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NCT00940225 · FLOW

Participant flow

Study of Cabozantinib (XL184) in Adults With Advanced Malignancies · Source last updated 2024-04-25

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups
  1. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG000
    title
    RDT Cohort - Castration-Resistant Prostate Cancer (CRPC)
  2. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG001
    title
    RDT Cohort - Melanoma
  3. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG002
    title
    RDT Cohort - Non-Small Cell Lung Cancer (NSCLC)
  4. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG003
    title
    RDT Cohort - Pancreatic Cancer
  5. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG004
    title
    RDT Cohort - Gastric/Gastroesophageal Junction Cancer (GEJ)
  6. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG005
    title
    RDT Cohort - Hepatocellular Carcinoma (HCC)
  7. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG006
    title
    RDT Cohort - Small Cell Lung Cancer (SCLC)
  8. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG007
    title
    RDT Cohort - Ovarian Cancer
  9. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG008
    title
    RDT Cohort - Metastatic Breast Cancer (MBC)
  10. description
    Subjects received a single oral daily dose of cabozantinib at 100 mg.
    id
    FG009
    title
    NRE Cohort - CRPC 100 mg
  11. description
    Subjects received a single oral daily dose of cabozantinib at 39.4 mg.
    id
    FG010
    title
    NRE Cohort - CRPC 39.4 mg
  12. description
    Subjects received a single oral daily dose of cabozantinib at 100 mg.
    id
    FG011
    title
    NRE Cohort - Ovarian Cancer 100mg
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        171
      2. group Id
        FG001
        num Subjects
        77
      3. group Id
        FG002
        num Subjects
        60
      4. group Id
        FG003
        num Subjects
        20
      5. group Id
        FG004
        num Subjects
        21
      6. group Id
        FG005
        num Subjects
        41
      7. group Id
        FG006
        num Subjects
        21
      8. group Id
        FG007
        num Subjects
        70
      9. group Id
        FG008
        num Subjects
        45
      10. group Id
        FG009
        num Subjects
        93
      11. group Id
        FG010
        num Subjects
        51
      12. group Id
        FG011
        num Subjects
        60
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        66
      3. group Id
        FG002
        num Subjects
        47
      4. group Id
        FG003
        num Subjects
        16
      5. group Id
        FG004
        num Subjects
        19
      6. group Id
        FG005
        num Subjects
        36
      7. group Id
        FG006
        num Subjects
        20
      8. group Id
        FG007
        num Subjects
        60
      9. group Id
        FG008
        num Subjects
        41
      10. group Id
        FG009
        num Subjects
        87
      11. group Id
        FG010
        num Subjects
        48
      12. group Id
        FG011
        num Subjects
        54
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        15
      2. group Id
        FG001
        num Subjects
        11
      3. group Id
        FG002
        num Subjects
        13
      4. group Id
        FG003
        num Subjects
        4
      5. group Id
        FG004
        num Subjects
        2
      6. group Id
        FG005
        num Subjects
        5
      7. group Id
        FG006
        num Subjects
        1
      8. group Id
        FG007
        num Subjects
        10
      9. group Id
        FG008
        num Subjects
        4
      10. group Id
        FG009
        num Subjects
        6
      11. group Id
        FG010
        num Subjects
        3
      12. group Id
        FG011
        num Subjects
        6
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG000
    title
    RDT Cohort - Castration-Resistant Prostate Cancer (CRPC)
  2. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG001
    title
    RDT Cohort - Melanoma
  3. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG002
    title
    RDT Cohort - Non-Small Cell Lung Cancer (NSCLC)
  4. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG003
    title
    RDT Cohort - Pancreatic Cancer
  5. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG004
    title
    RDT Cohort - Gastric/Gastroesophageal Junction Cancer (GEJ)
  6. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG005
    title
    RDT Cohort - Hepatocellular Carcinoma (HCC)
  7. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG006
    title
    RDT Cohort - Small Cell Lung Cancer (SCLC)
  8. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG007
    title
    RDT Cohort - Ovarian Cancer
  9. description
    Eligible subjects with advanced solid tumors received open-label cabozantinib at a starting daily dose of 100 mg (freebase weight).
    id
    FG008
    title
    RDT Cohort - Metastatic Breast Cancer (MBC)
  10. description
    Subjects received a single oral daily dose of cabozantinib at 100 mg.
    id
    FG009
    title
    NRE Cohort - CRPC 100 mg
  11. description
    Subjects received a single oral daily dose of cabozantinib at 39.4 mg.
    id
    FG010
    title
    NRE Cohort - CRPC 39.4 mg
  12. description
    Subjects received a single oral daily dose of cabozantinib at 100 mg.
    id
    FG011
    title
    NRE Cohort - Ovarian Cancer 100mg
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        171
      2. group Id
        FG001
        num Subjects
        77
      3. group Id
        FG002
        num Subjects
        60
      4. group Id
        FG003
        num Subjects
        20
      5. group Id
        FG004
        num Subjects
        21
      6. group Id
        FG005
        num Subjects
        41
      7. group Id
        FG006
        num Subjects
        21
      8. group Id
        FG007
        num Subjects
        70
      9. group Id
        FG008
        num Subjects
        45
      10. group Id
        FG009
        num Subjects
        93
      11. group Id
        FG010
        num Subjects
        51
      12. group Id
        FG011
        num Subjects
        60
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        66
      3. group Id
        FG002
        num Subjects
        47
      4. group Id
        FG003
        num Subjects
        16
      5. group Id
        FG004
        num Subjects
        19
      6. group Id
        FG005
        num Subjects
        36
      7. group Id
        FG006
        num Subjects
        20
      8. group Id
        FG007
        num Subjects
        60
      9. group Id
        FG008
        num Subjects
        41
      10. group Id
        FG009
        num Subjects
        87
      11. group Id
        FG010
        num Subjects
        48
      12. group Id
        FG011
        num Subjects
        54
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        15
      2. group Id
        FG001
        num Subjects
        11
      3. group Id
        FG002
        num Subjects
        13
      4. group Id
        FG003
        num Subjects
        4
      5. group Id
        FG004
        num Subjects
        2
      6. group Id
        FG005
        num Subjects
        5
      7. group Id
        FG006
        num Subjects
        1
      8. group Id
        FG007
        num Subjects
        10
      9. group Id
        FG008
        num Subjects
        4
      10. group Id
        FG009
        num Subjects
        6
      11. group Id
        FG010
        num Subjects
        3
      12. group Id
        FG011
        num Subjects
        6
      type
      NOT COMPLETED
    title
    Overall Study

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Preserved source evidence · Not medical advice