NCT00748657 · 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 21 days until disease progression or adverse effects prohibit further treatment
- id
- FG000
- title
- Bevacizumab
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 9/22/2008 and closed to accrual on 1/31/2011 (suspended from 1/4/2010 to 8/9/2010).
Complete source fields
- groups
- description
- Bevacizumab 15 mg/kg IV every 21 days until disease progression or adverse effects prohibit further treatment
- id
- FG000
- title
- Bevacizumab
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 36
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 9/22/2008 and closed to accrual on 1/31/2011 (suspended from 1/4/2010 to 8/9/2010).
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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