NCT00022659 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Bevacizumab 15 mg/kg IV, every 3 weeks (one cycle) until disease progression or adverse effects prohibit further therapy
- id
- FG000
- title
- Bevacizumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Ineligible: wrong primary
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Never treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 64
- type
- STARTED
- achievements
- comment
- Eligible and treated patients.
- group Id
- FG000
- num Subjects
- 62
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 4/29/2002 and closed to accrual on 8/25/2004 (suspended from 10/6/2003 to 12/1/2003).
Complete source fields
- groups
- description
- Bevacizumab 15 mg/kg IV, every 3 weeks (one cycle) until disease progression or adverse effects prohibit further therapy
- id
- FG000
- title
- Bevacizumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Ineligible: wrong primary
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Never treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 64
- type
- STARTED
- achievements
- comment
- Eligible and treated patients.
- group Id
- FG000
- num Subjects
- 62
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 4/29/2002 and closed to accrual on 8/25/2004 (suspended from 10/6/2003 to 12/1/2003).
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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