NCT00096122 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Cytarabine 1.5 g/m\^2 and Idarubicin 12 mg/m\^2 intravenous (IV) continuously on days 1-3 (or 1-4), with Oral Tipifarnib 200/300 twice daily on days 1-21, repeats every 21 days.
- id
- FG000
- title
- Idarubicin, Cytarabine + Tipifarnib
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 95
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 95
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- One participant enrolled was excluded from the study.
- recruitment Details
- Recruitment Period: 9/16/2004 to 9/22/2006. All patients registered at The University of Texas M.D. Anderson Cancer Center.
Complete source fields
- groups
- description
- Cytarabine 1.5 g/m\^2 and Idarubicin 12 mg/m\^2 intravenous (IV) continuously on days 1-3 (or 1-4), with Oral Tipifarnib 200/300 twice daily on days 1-21, repeats every 21 days.
- id
- FG000
- title
- Idarubicin, Cytarabine + Tipifarnib
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 95
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 95
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- One participant enrolled was excluded from the study.
- recruitment Details
- Recruitment Period: 9/16/2004 to 9/22/2006. All patients registered at The University of Texas M.D. Anderson Cancer Center.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle