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NCT Number: NCT06359509

Study of SYS6020 in BCMA-positive Multiple Myeloma

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. ≥ 18 years of age at the time of signing informed consent;
  • 2. Cytology or tissue biopsy meets diagnostic criteria for multiple myeloma (according to IMWG criteria);
  • 3. Bone marrow specimens confirmed positive BCMA expression in plasma cells and myeloma cells by immunohistochemistry or flow cytometry (>5%);
  • 4. 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)
  • 5. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1;
  • 6. Diagnosis of MM with relapsed or refractory disease and have had at least 1 prior lines of therapy.

Exclusion criteria

  • 1. Patients with plasmacytic leukemia or Waldenstrom's macroglobulinemia or POEMS syndrome (polyneuropathy, organ enlargement, endocrinopathy, monoclonal protein and skin lesions) or amyloidosis at screening;
  • 2. Received any prior CAR-T therapy or BCMA targeted therapy;
  • 3. Patients who have received autologous hematopoietic stem cell transplantation (ASCT) within 12 weeks prior to monocyte collection or history of allogeneic stem cell transplantation;
  • 4. A history of immunodeficiency, including a positive HIV antibody test;
  • 5. 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);
  • 6. 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;
  • 7. History of Bacillus Tuberculosis (TB) treatment within 2 years prior to first medication;
  • 8. Patients with a history of interstitial lung disease and/or severe lung function impairment;
  • 9. Have an active bacterial, fungal, or viral infection;
  • 10.A history of severe cardiovascular disease.

Treatment and study plan

BCMA Targeted CAR T-cells

Biological

Each patient will receive BCMA Targeted CAR T-cells by intravenous infusion.

Primary outcomes

  1. Incidence of adverse events (AEs)

    Time frame: Up to approximately 6 months

    Incidence of adverse events (AEs)

  2. Dose limiting toxicities (DLTs)

    Time frame: Up to 21 days

    Dose limiting toxicities (DLTs)

Secondary outcomes

  1. Overall response rate (ORR)

    Time frame: Up to approximately 6 months

    Overall response rate (ORR)

  2. Percentage of subjects who achieved complete response or strict complete response (CR/sCR)

    Time frame: Up to approximately 6 months

    Percentage of subjects who achieved complete response or strict complete response (CR/sCR)

  3. Percentage of subjects who achieved very good partial response (VGPR) and higher response rate

    Time frame: Up to approximately 6 months

    Percentage of subjects who achieved very good partial response (VGPR) and higher response rate

Sponsors and collaborators

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Other

Registry information

Official study title

A Phase І Study of BCMA-targeted Chimeric Antigen Receptor T Cell (SYS6020) Injection in Relapsed or Refractory Multiple Myeloma

Important dates

Study start
2024
Primary completion
2027
Study completion
2032
First posted
Apr 11, 2024
Registry last updated
Apr 11, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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