NCT03690388 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- cabozantinib (60 mg) once daily orally (qd) Cabozantinib: Tablets containing 60-mg or 20-mg cabozantinib once daily orally.
- id
- FG000
- title
- Cabozantinib
- description
- placebo once daily orally (qd) Placebo: Tablets containing placebo equivalent of 60-mg or 20-mg cabozantinib once daily orally.
- id
- FG001
- title
- Placebo
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 29
- type
- Radiographic Progression
- reasons
- group Id
- FG000
- num Subjects
- 10
- group Id
- FG001
- num Subjects
- 6
- type
- Clinical deterioration
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 125
- group Id
- FG001
- num Subjects
- 62
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 89
- group Id
- FG001
- num Subjects
- 26
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 36
- group Id
- FG001
- num Subjects
- 36
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- cabozantinib (60 mg) once daily orally (qd) Cabozantinib: Tablets containing 60-mg or 20-mg cabozantinib once daily orally.
- id
- FG000
- title
- Cabozantinib
- description
- placebo once daily orally (qd) Placebo: Tablets containing placebo equivalent of 60-mg or 20-mg cabozantinib once daily orally.
- id
- FG001
- title
- Placebo
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 29
- type
- Radiographic Progression
- reasons
- group Id
- FG000
- num Subjects
- 10
- group Id
- FG001
- num Subjects
- 6
- type
- Clinical deterioration
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 125
- group Id
- FG001
- num Subjects
- 62
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 89
- group Id
- FG001
- num Subjects
- 26
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 36
- group Id
- FG001
- num Subjects
- 36
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
Triangle