NCT00621244 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every week, as part of a 28-day treatment cycle. Group X indications (AML, CML-BC, AP, CP, ALL, MDS (RAEB-1, -2), MMM, CMML, aCML, CLL, and PLL) is a sub-arm, based on disease indication.
- id
- FG000
- title
- Arm 1, Group X
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every week, as part of a 28-day treatment cycle. Group Y indications (MM, HL, and NHL) is a sub-arm, based on disease indication.
- id
- FG001
- title
- Arm 1, Group Y
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every other week, as part of a 28-day treatment cycle. Group X indications (AML, CML-BC, AP, CP, ALL, MDS (RAEB-1, -2), MMM, CMML, aCML, CLL, and PLL) is a sub-arm, based on disease indication.
- id
- FG002
- title
- Arm 2, Group X
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every other week, as part of a 28-day treatment cycle. Group Y indications (MM, HL, and NHL) is a sub-arm, based on disease indication.
- id
- FG003
- title
- Arm 2, Group Y
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 44
- group Id
- FG001
- num Subjects
- 20
- group Id
- FG002
- num Subjects
- 20
- group Id
- FG003
- num Subjects
- 15
- type
- Disease progression
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 27
- group Id
- FG001
- num Subjects
- 7
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 2
- type
- Administrative problems
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 86
- group Id
- FG001
- num Subjects
- 34
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 23
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 86
- group Id
- FG001
- num Subjects
- 34
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 23
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every week, as part of a 28-day treatment cycle. Group X indications (AML, CML-BC, AP, CP, ALL, MDS (RAEB-1, -2), MMM, CMML, aCML, CLL, and PLL) is a sub-arm, based on disease indication.
- id
- FG000
- title
- Arm 1, Group X
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every week, as part of a 28-day treatment cycle. Group Y indications (MM, HL, and NHL) is a sub-arm, based on disease indication.
- id
- FG001
- title
- Arm 1, Group Y
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every other week, as part of a 28-day treatment cycle. Group X indications (AML, CML-BC, AP, CP, ALL, MDS (RAEB-1, -2), MMM, CMML, aCML, CLL, and PLL) is a sub-arm, based on disease indication.
- id
- FG002
- title
- Arm 2, Group X
- description
- panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF), every other week, as part of a 28-day treatment cycle. Group Y indications (MM, HL, and NHL) is a sub-arm, based on disease indication.
- id
- FG003
- title
- Arm 2, Group Y
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 44
- group Id
- FG001
- num Subjects
- 20
- group Id
- FG002
- num Subjects
- 20
- group Id
- FG003
- num Subjects
- 15
- type
- Disease progression
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 27
- group Id
- FG001
- num Subjects
- 7
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 2
- type
- Administrative problems
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 86
- group Id
- FG001
- num Subjects
- 34
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 23
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 86
- group Id
- FG001
- num Subjects
- 34
- group Id
- FG002
- num Subjects
- 33
- group Id
- FG003
- num Subjects
- 23
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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