OncoMatch/Clinical Trials/NCT06581640
Chimeric Antigen Receptor Modified T Cells Targeting BCMA for the Treatment of Relapsed/Refractory Multiple Myeloma
Is NCT06581640 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies CAR-T treatment for multiple myeloma.
Treatment: CAR-T treatment — To evaluate the safety and tolerability of chimeric antigen receptor gene-modified T cells targeting BCMA for the treatment of relapsed/refractory multiple myeloma
Check if I qualifyExtracted eligibility criteria
Cancer type
Multiple Myeloma
Biomarker criteria
Required: BCMA (TNFRSF17) overexpression (positive)
Flow cytometry or histology confirms positive BCMA expression in myeloma cells
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Cannot have received: BCMA-targeted therapy
Previously received treatment targeting BCMA
Cannot have received: autologous hematopoietic stem cell transplantation
Exception: within the last 6 weeks
Underwent autologous hematopoietic stem cell transplantation within the last 6 weeks
Cannot have received: experimental drug
Exception: within the last 3 months
Received other experimental drug treatments within the last 3 months
Lab requirements
Blood counts
ALC ≥0.5 ×10^9/L, PLT >30×10^9/L, Hb >80 g/L
Kidney function
creatinine clearance rate >30 mL/min
Liver function
ALT and AST ≤2.5×ULN, those with liver involvement can be relaxed to ≤5×ULN; serum total bilirubin <34 μmol/L
Cardiac function
heart ejection fraction (EF) ≥40%, no pericardial effusion and significant arrhythmia; indoor SpO2 ≥92%
The patient has good liver, kidney, heart, and lung function: ALT and AST ≤2.5×ULN, those with liver involvement can be relaxed to ≤5×ULN; serum total bilirubin <34 μmol/L; creatinine clearance rate >30 mL/min; heart ejection fraction (EF) ≥40%, no pericardial effusion and significant arrhythmia; indoor SpO2 ≥92%
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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