NCT00054639 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Oblimersen 3 mg/kg/day continuous intravenous infusion daily for 7 days on alternated weeks on week 1, 3 and 5 (days 1 through 7, 15 through 21, and 29 through 35); Rituximab 375 mg/m2 intravenous infusion for six doses on days 3, 8,15, 22, 29, and 36.
- id
- FG000
- title
- Oblimersen + Rituximab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Physician Decision
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 48
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Two participants enrolled but not assigned were not included in baseline measures. Of the total 48 participants enrolled, 42 were evaluable for response and 46 for toxicity.
- recruitment Details
- Recruitment Period: January 07, 2003 to October 01, 2005. Recruitment was done at UT MD Anderson Cancer Center Clinics.
Complete source fields
- groups
- description
- Oblimersen 3 mg/kg/day continuous intravenous infusion daily for 7 days on alternated weeks on week 1, 3 and 5 (days 1 through 7, 15 through 21, and 29 through 35); Rituximab 375 mg/m2 intravenous infusion for six doses on days 3, 8,15, 22, 29, and 36.
- id
- FG000
- title
- Oblimersen + Rituximab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Physician Decision
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 48
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Two participants enrolled but not assigned were not included in baseline measures. Of the total 48 participants enrolled, 42 were evaluable for response and 46 for toxicity.
- recruitment Details
- Recruitment Period: January 07, 2003 to October 01, 2005. Recruitment was done at UT MD Anderson Cancer Center Clinics.
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Preserved source evidence · Not medical advice
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