drugset / Trial / NCT01045460

Trial of Activated Marrow Infiltrating Lymphocytes Alone or in Conjunction With an Allogeneic Granulocyte Macrophage Colony-stimulating Factor (GM-CSF)-Based Myeloma Cellular Vaccine in the Autologous Transplant Setting in Multiple Myeloma

NCT01045460

RandomizedParallel-groupOpen-labelTreatment

Summary

Patient Population: Patients with active myeloma (Stage II/III) that have completed induction therapy and are eligible for an autologous stem cell transplant. Number of Patients: Will treat a total of 32 evaluable patients in a 1:1 randomization of aMILs vs aMILs plus vaccine. An evaluable patient is defined as one which has received the activated MILs and is at least 6 months post-transplant. Study Objectives: Disease response as determined by the Blade' criteria will be the primary endpoint of the trial at one year. Additional study endpoints include progression free survival, parameters of T cell reconstitution, anti-tumor immune responses as well as the effect on osteoclastogenesis and clonogenic myeloma precursor cells.

Timeline

Start
2010-01-15
Primary completion
2014-12
Completion
2020-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Activated marrow infiltrating lymphocytes Unknown
Subject Allogeneic Myeloma Vaccine Vaccine
Background Cyclophosphamide Other / unclassified 2.5 g
Background Melphalan Small molecule 100 mg
Background filgrastim Protein / enzyme biologic

Indications