Monoclonal Antibody Therapy in Treating Patients With Non-Hodgkin's Lymphoma

PHASE3TerminatedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

November 30, 1998

Primary Completion Date

April 30, 2002

Study Completion Date

November 30, 2012

Conditions
Lymphoma
Interventions
RADIATION

tositumomab and iodine I 131 tositumomab

Dosimetric Dose:Unlabeled anti-B1 (450mg) will be given as peripheral or central IV infusion over one hour or longer depending upon rate-dependent side effects. A trace-labeled dose of 131I-anti-B will be infused over 20 minutes, if rate-dependent side effects permit. An amount of unlabeled Anti-B1 Antibody is added to the 5 mCi of Iodine-131 Anti-B1 Antibody sufficient to result in a final amount of 35 mg of Anti-B1 antibody. On study Day 7 (may be delayed up to study Day 14), patients will receive the therapeutic dose, which consists of an infusion of 450mg of Anti-B1 Antibody followed by an infusion of Iodine-131 Anti-B1 Antibody.

Trial Locations (1)

68198-3330

University of Nebraska Medical Center, Omaha

Sponsors
All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

collaborator

Coulter Pharmaceutical, Inc.

INDUSTRY

lead

University of Nebraska

OTHER

NCT00004874 - Monoclonal Antibody Therapy in Treating Patients With Non-Hodgkin's Lymphoma | Biotech Hunter | Biotech Hunter