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NCT01908426 · FLOW

Participant flow

Study of Cabozantinib (XL184) vs Placebo in Subjects With Hepatocellular Carcinoma Who Have Received Prior Sorafenib · Source last updated 2021-05-06

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

groups
  1. description
    Cabozantinib (XL184) 60 mg tablet once daily Cabozantinib tablets
    id
    FG000
    title
    Cabozantinib (XL184)
  2. description
    Oral cabozantinib-matched placebo tablet once daily Placebo tablets
    id
    FG001
    title
    Placebo
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        98
      2. group Id
        FG001
        num Subjects
        11
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        72
      2. group Id
        FG001
        num Subjects
        38
      type
      Clinical Deterioration
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        1
      type
      Lost to Follow-up
    5. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        3
      type
      Physician Decision
    6. reasons
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        6
      type
      Withdrawal by Subject
    7. reasons
      1. group Id
        FG000
        num Subjects
        206
      2. group Id
        FG001
        num Subjects
        152
      type
      Progressive Disease
    8. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Protocol Violation
    9. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      No Study Treatment Given
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        470
      2. group Id
        FG001
        num Subjects
        237
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        73
      2. group Id
        FG001
        num Subjects
        26
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        397
      2. group Id
        FG001
        num Subjects
        211
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
First patient enrolled: 26 September 2013, Data cut-off date: 01 June 2017
Complete source fields
groups
  1. description
    Cabozantinib (XL184) 60 mg tablet once daily Cabozantinib tablets
    id
    FG000
    title
    Cabozantinib (XL184)
  2. description
    Oral cabozantinib-matched placebo tablet once daily Placebo tablets
    id
    FG001
    title
    Placebo
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        98
      2. group Id
        FG001
        num Subjects
        11
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        72
      2. group Id
        FG001
        num Subjects
        38
      type
      Clinical Deterioration
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        1
      type
      Lost to Follow-up
    5. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        3
      type
      Physician Decision
    6. reasons
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        6
      type
      Withdrawal by Subject
    7. reasons
      1. group Id
        FG000
        num Subjects
        206
      2. group Id
        FG001
        num Subjects
        152
      type
      Progressive Disease
    8. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Protocol Violation
    9. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      No Study Treatment Given
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        470
      2. group Id
        FG001
        num Subjects
        237
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        73
      2. group Id
        FG001
        num Subjects
        26
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        397
      2. group Id
        FG001
        num Subjects
        211
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
First patient enrolled: 26 September 2013, Data cut-off date: 01 June 2017

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Preserved source evidence · Not medical advice