NCT02654990 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants received 20 milligrams (mg) panobinostat thrice a week (TIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG000
- title
- Arm A - Panobinostat (20 mg, TIW)
- description
- Participants received 20 mg panobinostat twice a week (BIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG001
- title
- Arm B - Panobinostat (20 mg, BIW)
- description
- Participants received 10 mg panobinostat TIW, 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG002
- title
- Arm C - Panobinostat (10 mg, TIW)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 82
- group Id
- FG001
- num Subjects
- 83
- group Id
- FG002
- num Subjects
- 83
- comment
- Full analysis set (FAS): all participants to whom study treatment was assigned by randomization.
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 79
- group Id
- FG001
- num Subjects
- 82
- group Id
- FG002
- num Subjects
- 80
- comment
- Safety Set: all participants who received any study treatment.
- type
- Received at Least 1 Dose of Study Drug
- achievements
- group Id
- FG000
- num Subjects
- 82
- group Id
- FG001
- num Subjects
- 83
- group Id
- FG002
- num Subjects
- 83
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Participants received 20 milligrams (mg) panobinostat thrice a week (TIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG000
- title
- Arm A - Panobinostat (20 mg, TIW)
- description
- Participants received 20 mg panobinostat twice a week (BIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG001
- title
- Arm B - Panobinostat (20 mg, BIW)
- description
- Participants received 10 mg panobinostat TIW, 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
- id
- FG002
- title
- Arm C - Panobinostat (10 mg, TIW)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 82
- group Id
- FG001
- num Subjects
- 83
- group Id
- FG002
- num Subjects
- 83
- comment
- Full analysis set (FAS): all participants to whom study treatment was assigned by randomization.
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 79
- group Id
- FG001
- num Subjects
- 82
- group Id
- FG002
- num Subjects
- 80
- comment
- Safety Set: all participants who received any study treatment.
- type
- Received at Least 1 Dose of Study Drug
- achievements
- group Id
- FG000
- num Subjects
- 82
- group Id
- FG001
- num Subjects
- 83
- group Id
- FG002
- num Subjects
- 83
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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