Relapsed or progressive disease after at least 1 prior chemotherapy requiring treatment.
Bidimensionally measurable disease with at least 1 lesion \>= 2.0 cm in a single dimension.
Acceptable hematologic, hepatic, and renal function parameters.
Recovered fully from any significant toxicity associated with prior surgery, radiation treatments, chemotherapy, biological therapy, autologous bone marrow or stem cell transplant, or investigational drugs.
You may not be if
Follicular lymphoma Grade 3b.
Rituximab refractory or refractory to anti-CD20 radioimmunotherapy (no response to prior rituximab or prior rituximab-containing regimen, or a response with a TTP of less than 6 months).
Cancer radiotherapy, biological therapy, or chemotherapy within 3 weeks prior to Study Day 1 (6 weeks if nitrosourea or mitomycin C).
Prior lymphoma vaccine therapy within 12 months prior to Study Day 1.
Prior antibody therapy for lymphoma (including radioimmunotherapy) within 6 months prior to Study Day 1.
Autologous bone marrow or stem cell transplant within 6 months prior to Study Day 1.
Prior allogeneic transplant.
Transfusion-dependent subjects.
Another primary malignancy requiring active treatment (except hormonal therapy).
Serious nonmalignant disease (e.g., congestive heart failure, hydronephrosis); active uncontrolled bacterial, viral, or fungal infections; or other conditions, which would compromise protocol objectives in the opinion of the Investigator and/or the Sponsor.
New York Heart Association Class III or IV cardiac disease or myocardial infarction within 6 months prior to Study Day 1.
Clareo Health | A Study of Galiximab + Rituximab Versus Rituximab + Placebo in Follicular Non-Hodgkin's Lymphoma (NHL)
