NCT01667419 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- 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
- 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
- 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
- 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
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- Reason Not Specified
- reasons
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 8
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 8
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- type
- Non-compliance
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 4
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 18
- group Id
- FG001
- num Subjects
- 33
- group Id
- FG002
- num Subjects
- 25
- group Id
- FG003
- num Subjects
- 26
- type
- Death
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 157
- group Id
- FG001
- num Subjects
- 157
- group Id
- FG002
- num Subjects
- 93
- group Id
- FG003
- num Subjects
- 91
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 110
- group Id
- FG002
- num Subjects
- 57
- group Id
- FG003
- num Subjects
- 52
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 43
- group Id
- FG001
- num Subjects
- 47
- group Id
- FG002
- num Subjects
- 36
- group Id
- FG003
- num Subjects
- 39
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- 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
- 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
- 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
- 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
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- Reason Not Specified
- reasons
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 8
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 8
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- type
- Non-compliance
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 6
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 4
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 18
- group Id
- FG001
- num Subjects
- 33
- group Id
- FG002
- num Subjects
- 25
- group Id
- FG003
- num Subjects
- 26
- type
- Death
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 157
- group Id
- FG001
- num Subjects
- 157
- group Id
- FG002
- num Subjects
- 93
- group Id
- FG003
- num Subjects
- 91
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 110
- group Id
- FG002
- num Subjects
- 57
- group Id
- FG003
- num Subjects
- 52
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 43
- group Id
- FG001
- num Subjects
- 47
- group Id
- FG002
- num Subjects
- 36
- group Id
- FG003
- num Subjects
- 39
- type
- NOT COMPLETED
- title
- Overall Study
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