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
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.
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 →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.
Have measurable disease by International Myeloma Working Group (IMWG) criteria based on one or more of the following findings:
Exclusion Criteria:
Low, medium and high doses of SYS6020 will be given.
Biological: BCMA Targeted CAR T-cells
Each patient will receive BCMA Targeted CAR T-cells by intravenous infusion.
Incidence of adverse events (AEs)
Incidence of adverse events (AEs)
Time frame: Up to approximately 6 months
Dose limiting toxicities (DLTs)
Dose limiting toxicities (DLTs)
Time frame: Up to 21 days
Overall response rate (ORR)
Overall response rate (ORR)
Time frame: Up to approximately 6 months
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
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
No study locations are listed for this record.
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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Wuhan Union Hospital, China