Zevalin With Non Myeloablative Allogeneic Stem Cell Transplantation in Patients With Non Hodgkin Lymphoma
- Sponsor
- Maisonneuve-Rosemont Hospital
- Study ID
- NCT00807196
- Phase
- PHASE1/PHASE2
- Status
- Unknown
Conditions
- Non-Hodgkins Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Rituximab — DRUG250mg/m2 day -21 and day -14 of preparative regimen
- 90Y ibritumomab tiuxetan (Zevalin) — DRUG0.4 mCi/kg IV on day -14 of preparative regimen
- Cyclophosphamide — DRUG300mg/m2 IV daily for 5 days day -8 to day -4 of preparative regimen
- Fludarabine — DRUG30mg/m2 IV daily for 5 days day -8 to day -4 of preparative regimen
- Non myeloablative allogeneic stem cell transplantation — OTHERBlood stem cell infusion on day 0
Study Details
The purpose of this study is to investigate the ability to combine a radioactive medication directly targeted against lymphoma cells with the immune effects of an allogeneic blood stem cell transplant.
Key Dates
- Start date
- Sep 30, 2008
- Status verified
- Dec 2008
- Primary completion
- Dec 31, 2011
- Completion
- Dec 31, 2012
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: T
Primary Outcome Measure
Engraftment, chimerism, transplant related toxicity, acute and chronic GVHD [ Time Frame: one year ]
Central Contacts
- Thomas Kiss, MD514-252-3404
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