NCT00425750 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Docetaxel will be given first at 40 mg/m2 IV on days 1 and 8 of a 21-day cycle except the first dose is held only on Day 1 of Cycle 1. Immediately afterwards, Bortezomib will be given at 1.6 mg/m2 IV on days 1 and 8 of a 21-day cycle. The first dose is given as a single agent only on Day 1 of Cycle 1.
- id
- FG000
- title
- Bortezomib; Docetaxel
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 18
- type
- Progression of disease
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Twenty-seven patients consented, two of which were ineligible.
- recruitment Details
- This study was open to accrual from 8/25/2005 through 5/20/2008.
Complete source fields
- groups
- description
- Docetaxel will be given first at 40 mg/m2 IV on days 1 and 8 of a 21-day cycle except the first dose is held only on Day 1 of Cycle 1. Immediately afterwards, Bortezomib will be given at 1.6 mg/m2 IV on days 1 and 8 of a 21-day cycle. The first dose is given as a single agent only on Day 1 of Cycle 1.
- id
- FG000
- title
- Bortezomib; Docetaxel
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 18
- type
- Progression of disease
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Twenty-seven patients consented, two of which were ineligible.
- recruitment Details
- This study was open to accrual from 8/25/2005 through 5/20/2008.
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Preserved source evidence · Not medical advice
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