NCT00698685 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Pentostatin and Alemtuzumab as a Preparative Regimen for Allogeneic \[related or unrelated\] Hematopoietic SCT. Pentostatin: 4 mg/m2/24 hour IV continuously over 72 hours on days -8 to -6. Alemtuzumab: 20 mg per dose IV over 8 hours on days -5 to -1. Patients then received infusion of related or unrelated donor peripheral blood progenitor cells on day 0. Patients also receive cyclosporine IV continuously beginning on day -2, continuing (IV or orally) until day 100, followed by a taper.
- id
- FG000
- title
- Preparative Regimen of Pentostatin and Alemtuzumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Sister withdrew as donor
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Off study pre transplant by clinic MD
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 14
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 12
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Following consent process, subjects who consented to participate were screened per the selection criteria in the study.
- recruitment Details
- Following University of Arizona IRB review and approval, the study opened to accrual on November 2005 at the Arizona Cancer Center clinic and University Medical Center sites \[Tucson, Arizona\].
Complete source fields
- groups
- description
- Pentostatin and Alemtuzumab as a Preparative Regimen for Allogeneic \[related or unrelated\] Hematopoietic SCT. Pentostatin: 4 mg/m2/24 hour IV continuously over 72 hours on days -8 to -6. Alemtuzumab: 20 mg per dose IV over 8 hours on days -5 to -1. Patients then received infusion of related or unrelated donor peripheral blood progenitor cells on day 0. Patients also receive cyclosporine IV continuously beginning on day -2, continuing (IV or orally) until day 100, followed by a taper.
- id
- FG000
- title
- Preparative Regimen of Pentostatin and Alemtuzumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Sister withdrew as donor
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Off study pre transplant by clinic MD
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 14
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 12
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Following consent process, subjects who consented to participate were screened per the selection criteria in the study.
- recruitment Details
- Following University of Arizona IRB review and approval, the study opened to accrual on November 2005 at the Arizona Cancer Center clinic and University Medical Center sites \[Tucson, Arizona\].
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle