Ibritumomab Tiuxetan (Zevalin)+ Rituximab Maintenance
Status: | Terminated |
---|---|
Conditions: | Lymphoma, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 8/11/2018 |
Start Date: | January 25, 2005 |
End Date: | March 2013 |
Ibritumomab Tiuxetan Plus Rituximab as Initial Therapy for Patients With High Tumor Burden, Indolent Histology Non-Hodgkin's Lymphoma
Subjects will receive the Ibritumomab Tiuxetan (Zevalin) therapeutic regimen; then rituximab
consolidation and maintenance therapy every 3 months until disease progression
consolidation and maintenance therapy every 3 months until disease progression
The objective of this study is to estimate the median progression-free survival for patients
receiving this regimen, along with the rate of complete response at 6 months, toxicities
associated with this regimen, and laboratory correlates. Subjects will receive the
Ibritumomab Tiuxetan (Zevalin) therapeutic regimen; then rituximab consolidation and
maintenance therapy every 3 months until disease progression.
receiving this regimen, along with the rate of complete response at 6 months, toxicities
associated with this regimen, and laboratory correlates. Subjects will receive the
Ibritumomab Tiuxetan (Zevalin) therapeutic regimen; then rituximab consolidation and
maintenance therapy every 3 months until disease progression.
Inclusion Criteria:
- Patients with biopsy-proven non-hodgkins lymphoma of follicular grade 1, 2, or 3
- Meeting FLIPI criteria for intermediate or high risk.
- No prior chemotherapy, radiotherapy or immunotherapy for lymphoma;
- Patients may not have known HIV infection, and must not be Hepatitis B Surface Antigen
positive.
Exclusion Criteria:
- May not be pregnant or breastfeeding, have documented CNS (Central Nervous System)
disease, G-CSF (Granulocyte Colony Stimulating Facto) or GM-CSF
(Granulocyte/Macrophage Colony Stimulating Factor) within 2 weeks prior
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