Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Biogen
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Histologically confirmed, relapsed or refractory CD20+ follicular B-cell NHL within 12 months of Study Day 1 (without clinical evidence of transformation). NHL must require treatment as determined by an increase in overall tumor size. The presence of B symptoms, and/or the presence of masses which are causing ongoing clinical symptoms.
Bidimensionally measurable disease meeting the minimum requirement of at least 1 lesion \>/= 2.0 cm in a single dimension.
No lymphoma therapy for 3 weeks prior to Study Day 1.
Patients must be recovered from all toxicities associated with prior surgery, radiation therapy, chemotherapy, or immunotherapy.
Signed IRB-approved informed consent.
Greater than 18 years of age.
Expected survival \>/= 3 months.
WHO performance status of \</= 2.
Acceptable hematologic status, liver function, renal function, and pulmonary function.
Female patients who are not pregnant or lactating.
Men and women of reproductive potential who are following accepted birth control methods.
You may not be if
Patients with impaired bone marrow reserve, which may be indicated by prior myeloablative therapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell (PBSC) rescue.
Prior radioimmunotherapy, including the Zevalin regimen.
Prior immunotherapy, including Rituxan therapy within 6 months of Study Day 1.
Rituxan-refractory (no response to most recent Rituxan-containing regimen, or TTP was \< 6 months).
Presence of CNS lymphoma.
Patients with chronic lymphocytic leukemia (CLL).
Known history of HIV or AIDS.
Serious nonmalignant disease or infection
Major surgery, other than diagnostic surgery, within 4 weeks of Study Day 1.
Patients who received investigational product within 4 weeks of Study Day 1 or patients who may experience long-term toxicity from a previous investigational therapy.
Clareo Health | Safety and Efficacy of Zevalin in the Treatment of Non-Hodgkin's Lymphoma
