NCT00546377 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- To determine the dose of mitoxantrone that can be safely administered with pentostatin, cyclosphosphamide, and rituximab in previously treated patient with CLL and other low grade B-cell malignancies.
- id
- FG000
- title
- Pentostatin,Cyclophosphamide,Rituximab & Mitoxantrone
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Deemed ineligible
- reasons
- group Id
- FG000
- num Subjects
- 6
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 43
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- To determine the dose of mitoxantrone that can be safely administered with pentostatin, cyclosphosphamide, and rituximab in previously treated patient with CLL and other low grade B-cell malignancies.
- id
- FG000
- title
- Pentostatin,Cyclophosphamide,Rituximab & Mitoxantrone
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Deemed ineligible
- reasons
- group Id
- FG000
- num Subjects
- 6
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 43
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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