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NCT01667419 · FLOW

Participant flow

A Study of Vemurafenib Adjuvant Therapy in Participants With Surgically Resected Cutaneous BRAF-Mutant Melanoma · Source last updated 2019-07-23

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

groups
  1. description
    Participants with completely resected Stage IIC, IIIA, or IIIB cutaneous melanoma) received vemurafenib, 960 milligrams (mg) twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG000
    title
    Cohort 1 Vemurafenib
  2. description
    Participants with completely resected Stage IIC, IIIA, or IIIB cutaneous melanoma) received vemurafenib-matching placebo twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG001
    title
    Cohort 1 Placebo
  3. description
    Participants with Stage IIIC cutaneous melanoma received vemurafenib, 960 mg twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG002
    title
    Cohort 2 Vemurafenib
  4. description
    Participants with Stage IIIC cutaneous melanoma received vemurafenib-matching placebo twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG003
    title
    Cohort 2 Placebo
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      Reason Not Specified
    2. reasons
      1. group Id
        FG000
        num Subjects
        16
      2. group Id
        FG001
        num Subjects
        8
      3. group Id
        FG002
        num Subjects
        9
      4. group Id
        FG003
        num Subjects
        8
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      Non-compliance
    4. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      Protocol Violation
    5. reasons
      1. group Id
        FG000
        num Subjects
        7
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        2
      4. group Id
        FG003
        num Subjects
        4
      type
      Lost to Follow-up
    6. reasons
      1. group Id
        FG000
        num Subjects
        18
      2. group Id
        FG001
        num Subjects
        33
      3. group Id
        FG002
        num Subjects
        25
      4. group Id
        FG003
        num Subjects
        26
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        157
      2. group Id
        FG001
        num Subjects
        157
      3. group Id
        FG002
        num Subjects
        93
      4. group Id
        FG003
        num Subjects
        91
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        110
      3. group Id
        FG002
        num Subjects
        57
      4. group Id
        FG003
        num Subjects
        52
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        43
      2. group Id
        FG001
        num Subjects
        47
      3. group Id
        FG002
        num Subjects
        36
      4. group Id
        FG003
        num Subjects
        39
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Participants with completely resected Stage IIC, IIIA, or IIIB cutaneous melanoma) received vemurafenib, 960 milligrams (mg) twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG000
    title
    Cohort 1 Vemurafenib
  2. description
    Participants with completely resected Stage IIC, IIIA, or IIIB cutaneous melanoma) received vemurafenib-matching placebo twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG001
    title
    Cohort 1 Placebo
  3. description
    Participants with Stage IIIC cutaneous melanoma received vemurafenib, 960 mg twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG002
    title
    Cohort 2 Vemurafenib
  4. description
    Participants with Stage IIIC cutaneous melanoma received vemurafenib-matching placebo twice daily, in 28-day cycles, for up to 52 weeks
    id
    FG003
    title
    Cohort 2 Placebo
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      Reason Not Specified
    2. reasons
      1. group Id
        FG000
        num Subjects
        16
      2. group Id
        FG001
        num Subjects
        8
      3. group Id
        FG002
        num Subjects
        9
      4. group Id
        FG003
        num Subjects
        8
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        1
      type
      Non-compliance
    4. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      Protocol Violation
    5. reasons
      1. group Id
        FG000
        num Subjects
        7
      2. group Id
        FG001
        num Subjects
        6
      3. group Id
        FG002
        num Subjects
        2
      4. group Id
        FG003
        num Subjects
        4
      type
      Lost to Follow-up
    6. reasons
      1. group Id
        FG000
        num Subjects
        18
      2. group Id
        FG001
        num Subjects
        33
      3. group Id
        FG002
        num Subjects
        25
      4. group Id
        FG003
        num Subjects
        26
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        157
      2. group Id
        FG001
        num Subjects
        157
      3. group Id
        FG002
        num Subjects
        93
      4. group Id
        FG003
        num Subjects
        91
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        110
      3. group Id
        FG002
        num Subjects
        57
      4. group Id
        FG003
        num Subjects
        52
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        43
      2. group Id
        FG001
        num Subjects
        47
      3. group Id
        FG002
        num Subjects
        36
      4. group Id
        FG003
        num Subjects
        39
      type
      NOT COMPLETED
    title
    Overall Study

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice