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Spots Global Cancer Trial Database for Safety Study of NHL With 90Y-hLL2 IgG

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Trial Identification

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

Interventions

90Y-hLL2

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: William A Wegener, MD, PhD

Affiliation: Gilead Sciences

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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