NCT01613768 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Eribulin mesylate (1.4 mg/m2) administered intravenously (IV) over 2-5 minutes on days 1 and 8 of a 21 day cycle. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Treatment (Eribulin Mesylate)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 29
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 29
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Twenty-nine patients were consented and treated.
- recruitment Details
- Seattle Cancer Care Alliance/University of Washington Phase II open label study enrolled patients at a single site between May 2012 and August 2015.
Complete source fields
- groups
- description
- Eribulin mesylate (1.4 mg/m2) administered intravenously (IV) over 2-5 minutes on days 1 and 8 of a 21 day cycle. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Treatment (Eribulin Mesylate)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 29
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 29
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Twenty-nine patients were consented and treated.
- recruitment Details
- Seattle Cancer Care Alliance/University of Washington Phase II open label study enrolled patients at a single site between May 2012 and August 2015.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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