NCT03465722 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- 300 mg PO QD avapritinib: Avapritinib tablets for oral administration. Avapritinib will be dosed at 300 mg once daily, continuously.
- id
- FG000
- title
- Avapritinib
- description
- 160 mg PO QD regorafenib: Regorafenib tablets for oral administration. Regorafenib will be dosed at 160 mg once daily for 3 weeks out of every 4 weeks (ie. 3 weeks on/1 week off).
- id
- FG001
- title
- Regorafinib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 21
- group Id
- FG001
- num Subjects
- 14
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 89
- group Id
- FG001
- num Subjects
- 87
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 3
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 33
- group Id
- FG001
- num Subjects
- 32
- type
- Administrative/Other
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 2
- type
- Not treated
- reasons
- group Id
- FG000
- num Subjects
- 91
- group Id
- FG001
- num Subjects
- 98
- type
- Sponsor decision
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 240
- group Id
- FG001
- num Subjects
- 236
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 240
- group Id
- FG001
- num Subjects
- 236
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- 300 mg PO QD avapritinib: Avapritinib tablets for oral administration. Avapritinib will be dosed at 300 mg once daily, continuously.
- id
- FG000
- title
- Avapritinib
- description
- 160 mg PO QD regorafenib: Regorafenib tablets for oral administration. Regorafenib will be dosed at 160 mg once daily for 3 weeks out of every 4 weeks (ie. 3 weeks on/1 week off).
- id
- FG001
- title
- Regorafinib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 21
- group Id
- FG001
- num Subjects
- 14
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 89
- group Id
- FG001
- num Subjects
- 87
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 3
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 33
- group Id
- FG001
- num Subjects
- 32
- type
- Administrative/Other
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 2
- type
- Not treated
- reasons
- group Id
- FG000
- num Subjects
- 91
- group Id
- FG001
- num Subjects
- 98
- type
- Sponsor decision
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 240
- group Id
- FG001
- num Subjects
- 236
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 240
- group Id
- FG001
- num Subjects
- 236
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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