NCT00153920 · 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 intravenous bortezomib on a 3-week dosing cycle: 1.3 mg/m2 on days 1, 4, 8 and 11 followed by 10 day rest period for up to 8 cycles or for 2 cycles beyond complete response. Participants with progressive disease or unacceptable toxicity discontinued treatment.
- id
- FG000
- title
- Bortezomib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Progressive Disease
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Lack of Response
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal of Consent before Trt
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Progressive Disease before Trt
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 66
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 64
- type
- Eligible and Treated
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 30
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- 66 participants were enrolled between December 2003 and September 2005.
Complete source fields
- groups
- description
- Participants received intravenous bortezomib on a 3-week dosing cycle: 1.3 mg/m2 on days 1, 4, 8 and 11 followed by 10 day rest period for up to 8 cycles or for 2 cycles beyond complete response. Participants with progressive disease or unacceptable toxicity discontinued treatment.
- id
- FG000
- title
- Bortezomib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Progressive Disease
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Lack of Response
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal of Consent before Trt
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Progressive Disease before Trt
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 66
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 64
- type
- Eligible and Treated
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 30
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- 66 participants were enrolled between December 2003 and September 2005.
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Preserved source evidence · Not medical advice
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