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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 (Jun 2026). This Phase 2 trial studies CAR-T treatment for multiple myeloma.

Phase 2RecruitingThe First Affiliated Hospital of Xiamen UniversityNCT06581640Data as of Jun 2026Location: China

Treatment: CAR-T treatmentTo evaluate the safety and tolerability of chimeric antigen receptor gene-modified T cells targeting BCMA for the treatment of relapsed/refractory multiple myeloma

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Extracted eligibility criteria

Treatments studied

Other

CAR-T treatment

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)

Demographics

Ages ≤ 80

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.

Frequently asked questions

Is NCT06581640 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior BCMA-targeted therapy, autologous hematopoietic stem cell transplantation, experimental drug disqualifies patients from enrollment.

Does this trial require TNFRSF17?

Yes, TNFRSF17 overexpression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 80 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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