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Brief Title: Safety Study of NHL With 90Y-hLL2 IgG
Official Title: Phase I/II Radioimmunotherapy of Non-Hodgkin's Lymphoma With Radiolabeled Humanized IMMU-LL2: Treatment With 90Y-hLL2 IgG
Study ID: NCT00421395
Brief Summary: This will be an open label, multiple center, non-randomized, dose-escalation Phase I/II trial, designed to evaluate the safety and effectiveness of a repeated, outpatient regimen utilizing IMMU-hLL2 intact monoclonal antibody IgG labeled with different doses of 90Y for the treatment of patients B-cell lymphoma (NHL).
Detailed Description: 90Y-labeled hLL2 will be administered according to a schedule based upon whether or not a patient had prior high-dose chemotherapy with a marrow or stem cell transplant. Patients with both indolent and aggressive types of NHL will be enrolled at each dose level without segregation. However, at the conclusion of the trial, with the maximum tolerated dose (MTD) defined, a minimum number of 6 patients with indolent NHL, 6 patients with aggressive NHL, and 6 patients with \>25% bone marrow involvement will be studied at that dose level.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Unit 463 INSERM, Nantes, Cedex, France
Service des Maladies du Sang, Lille, , France
University Hospital Dresden, Dresden, , Germany
Klinikum der Georg-August-Universitat Gottingen, Gottingen, , Germany
Universitatsklinikum University of Saarland, Homburg/Saar, , Germany
Name: William A Wegener, MD, PhD
Affiliation: Gilead Sciences
Role: STUDY_CHAIR