Finding studies
Finding studies
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Lead
Thomas Martin, MD
PRIMARY OBJECTIVES: Dose Escalation: I. To evaluate the safety and toxicity of administering Chimeric Antigen Receptor T Cells (CAR-T) cells targeting BCMA to participants with Relapsed or Refractory Multiple Myeloma (RRMM). II. To determine the maximum tolerated dose (MTD) for anti-BCMA CAR-T cells. Dose Expansion: III. Determine whether administering conforming CAR T-cell product targeting BCMA to participants with RRMM increases the overall response rate (ORR) compared with historical data for non-CAR agents per International Myeloma Working Group (IMWG) response criteria. IV. Determine whether administering conforming CAR T-cell product targeting BCMA to participants with RRMM lowers the Grade 2 or greater neurologic events to \<10% in RRMM. SECONDARY OBJECTIVES: Dose Expansion: I. To describe the efficacy of conforming CAR-T cell product targeting BCMA in participants with RRMM. II. To evaluate the feasibility of manufacturing anti-BCMA CAR T-cells locally and ability to produce adequate quantities of vector positive T-cells. III. To evaluate the safety and toxicity of conforming CAR-T cell product targeting BCMA to participants with RRMM. EXPLORATORY OBJECTIVES: I. To determine the degree and impact of CAR-T persistence following anti-BCMA CAR-T cell infusion, on clinical outcomes and safety. II. Describe changes in health-related quality of life (HRQoL) using the European Organization for Research and Treatment of Cancer - Quality of Life C30 questionnaire (EORTC-QLQ-C30). III. To describe the efficacy of CAR-T cells targeting BCMA in participants with relapsed or refractory BCMA+ RRMM who were treated with product that did not meet one or more pre-specified release criteria (non-conforming product cohort). OUTLINE: Participants in both cohorts will undergo leukapheresis, receive lymphodepleting chemotherapy and then receive a single infusion of BCMA CAR-T therapy. After completion of study treatment, participants are followed up at 30, 60 and 90 days, 6 and 12 months, and then yearly for up to 15 years.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
