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Not yet recruitingNCT06359509Updated Apr 11, 2024

Study of SYS6020 in BCMA-positive Multiple Myeloma

An Early Phase 1 interventional study of BCMA Targeted CAR T-cells in Multiple Myeloma, sponsored by Wuhan Union Hospital, China. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-04-11.

Sponsored by Wuhan Union Hospital, China · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study 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.

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Conditions studied

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In context

Multiple Myeloma

3,632 studies on the registry are indexed under Multiple Myeloma; 745 are open to participants now.

This study's planned enrollment of 10 is below the median of 41 across 2,907 interventional studies indexed under Multiple Myeloma.

Browse Multiple Myeloma studies →

Lead sponsor

Wuhan Union Hospital, China is the lead sponsor of 230 studies on the registry; 104 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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;
    1. Received any prior CAR-T therapy or BCMA targeted therapy;
    1. Patients who have received autologous hematopoietic stem cell transplantation (ASCT) within 12 weeks prior to monocyte collection or history of allogeneic stem cell transplantation;
    1. A history of immunodeficiency, including a positive HIV antibody test;
    1. 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);
    1. 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;
    1. History of Bacillus Tuberculosis (TB) treatment within 2 years prior to first medication;
    1. Patients with a history of interstitial lung disease and/or severe lung function impairment;
    1. Have an active bacterial, fungal, or viral infection;
  • 10.A history of severe cardiovascular disease.
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Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    SYS6020

    Low, medium and high doses of SYS6020 will be given.

    Biological: BCMA Targeted CAR T-cells

Interventions

  • BiologicalBCMA Targeted CAR T-cells

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

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What researchers measure

Primary outcomes

  1. Incidence of adverse events (AEs)

    Incidence of adverse events (AEs)

    Time frame: Up to approximately 6 months

  2. Dose limiting toxicities (DLTs)

    Dose limiting toxicities (DLTs)

    Time frame: Up to 21 days

Secondary outcomes

  1. Overall response rate (ORR)

    Overall response rate (ORR)

    Time frame: Up to approximately 6 months

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

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

    Time frame: Up to approximately 6 months

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

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

    Time frame: Up to approximately 6 months

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06359509
Lead sponsor
Wuhan Union Hospital, China
Responsible party
MEI HENG (Proferssor Cheif Doctor, Wuhan Union Hospital, China) — Principal investigator
First posted
Apr 11, 2024
Start date
Apr 2024 (estimated)
Primary completion
May 2027 (estimated)
Completion
May 2032 (estimated)
Last update
Apr 11, 2024

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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