drugset / Trial / NCT01207765

Zevalin for Patients With Incomplete Response to Chemo Prior to Autologous Stem Cell Transplant for Multiple Myeloma

NCT01207765

NaSingle-groupOpen-labelTreatment

Summary

The study involves the use of a targeted form of radiation, in addition to standard high dose chemotherapy and stem cell transplant for multiple myeloma. The use of targeted radiation is designed to kill more multiple myeloma cells while avoiding the side effects of standard radiation. This type of targeted radiation (also known as radioimmunotherapy) has been approved by the Food and Drug Administration (FDA) for the treatment of a related disease, lymphoma under the trade name, Zevalin©. Zevalin© has been added to high dose chemotherapy and stem cell transplants for patients with lymphoma and is now being studied in this clinical trial for patients with multiple myeloma. This trial is only available at Tufts Medical Center. The proposed clinical trial will test whether CD20-targeted radio-immunotherapy can be safe and effective when integrated into a standard regimen of myeloablative chemotherapy and autologous stem cell rescue in patients with measurable disease prior to high dose chemotherapy and autologous stem cell transplant for multiple myeloma.

Timeline

Start
2008-04
Primary completion
2013-01
Completion
2013-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject 90Y Zevalin Monoclonal antibody 14.8 mbq/kg Intravenous
Subject Indium-111 ibritumomab tiuxetan Protein / enzyme biologic 1.5 mg Intravenous
Subject Indium-111 ibritumomab tiuxetan Protein / enzyme biologic 185 mbq Intravenous

Indications