Study of SYS6020 in BCMA-positive Multiple Myeloma
Early Phase 1
Not yet recruiting
- Conditions
- Multiple Myeloma
- Interventions
- Biological: BCMA Targeted CAR T-cells
- Registration Number
- NCT06359509
- Lead Sponsor
- Wuhan Union Hospital, China
- Brief Summary
This is a multi-center, phase I trial that studies the efficacy and recommended dose of BCMA CART cells in treating patients with BCMA-positive multiple myeloma (MM) that have not respond or relapsed after chemotherapy. B-cell maturation antigen (BCMA), a cell surface protein expressed on malignant plasma cell, has emerged as a very selective antigen to be targeted in novel immunotherapy for MM.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
-
- ≥ 18 years of age at the time of signing informed consent;
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- Cytology or tissue biopsy meets diagnostic criteria for multiple myeloma (according to IMWG criteria);
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- Bone marrow specimens confirmed positive BCMA expression in plasma cells and myeloma cells by immunohistochemistry or flow cytometry (>5%);
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- Have measurable disease by International Myeloma Working Group (IMWG) criteria based on one or more of the following findings:
- Serum M-protein≥ 1 g/dL（≥10 g/L）
- Urine M-protein ≥ 200 mg/24 hour
- Involved serum free light chain (FLCs) level≥10 mg/dL with FLCs abnormal ratio (<0.26或>1.65)
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- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1;
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- Diagnosis of MM with relapsed or refractory disease and have had at least 1 prior lines of therapy.
Exclusion Criteria
-
- Patients with plasmacytic leukemia or Waldenstrom's macroglobulinemia or POEMS syndrome (polyneuropathy, organ enlargement, endocrinopathy, monoclonal protein and skin lesions) or amyloidosis at screening;
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- Received any prior CAR-T therapy or BCMA targeted therapy;
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- Patients who have received autologous hematopoietic stem cell transplantation (ASCT) within 12 weeks prior to monocyte collection or history of allogeneic stem cell transplantation;
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- A history of immunodeficiency, including a positive HIV antibody test;
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- Hepatitis B surface antigen (HBsAg) positive and HBV-DNA above the lower limit of measurement or 1000 copies /mL (500 IU/mL), (whichever is lower), HCV antibody positive and HCV-RNA above the lower limit of measurement or 1000 copies /mL (whichever is lower);
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- Patients who, in the judgment of the investigator, need but are unable to receive prophylactic treatment for Pneumocystis, Herpes Simplex Virus (HSV), or Herpes Zoster (VZV) prior to initiation of treatment, or Syphilis confirmatory positive;
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- History of Bacillus Tuberculosis (TB) treatment within 2 years prior to first medication;
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- Patients with a history of interstitial lung disease and/or severe lung function impairment;
-
- Have an active bacterial, fungal, or viral infection;
- 10.A history of severe cardiovascular disease.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description SYS6020 BCMA Targeted CAR T-cells Low, medium and high doses of SYS6020 will be given.
- Primary Outcome Measures
Name Time Method Incidence of adverse events (AEs) Up to approximately 6 months Incidence of adverse events (AEs)
Dose limiting toxicities (DLTs) Up to 21 days Dose limiting toxicities (DLTs)
- Secondary Outcome Measures
Name Time Method Percentage of subjects who achieved complete response or strict complete response (CR/sCR) Up to approximately 6 months Percentage of subjects who achieved complete response or strict complete response (CR/sCR)
Percentage of subjects who achieved very good partial response (VGPR) and higher response rate Up to approximately 6 months Percentage of subjects who achieved very good partial response (VGPR) and higher response rate
Overall response rate (ORR) Up to approximately 6 months Overall response rate (ORR)