OncoMatch

OncoMatch/Clinical Trials/NCT06693973

An Early Clinical Study Evaluating the Safety and Efficacy of AcNK-Sup003 Cell Injection in the Treatment of Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma

Is NCT06693973 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies AcNK-Sup003 cell for b-cell non-hodgkin lymphoma (b-nhl).

Early Phase 1RecruitingUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyNCT06693973Data as of May 2026

Treatment: AcNK-Sup003 cellThe purpose of this study is to determine whether AcNK-Sup003 cell injection is safe and effective in the treatment of elapsed or refractory B-cell non-Hodgkin's lymphoma.

Check if I qualify

Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Biomarker criteria

Required: MS4A1 overexpression (CD20+)

Confirmed by pathology to have CD20+ relapsed or refractory B-cell non-Hodgkin's lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 2 prior lines

Must have received: CD20-targeted therapy — second-line or later

must have received CD20-targeted drugs [excluding CD20-negative tumors]

Must have received: anthracycline — second-line or later

must have received...anthracycline drugs

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: within 3 months before lymphodepletion

Received autologous hematopoietic stem cell transplantation or other autologous cell therapy products within 3 months before lymphodepletion

Cannot have received: allogeneic hematopoietic stem cell transplantation

Exception: within 6 months before lymphodepletion

received allogeneic hematopoietic stem cell transplantation or other allogeneic cell therapy products within 6 months before lymphodepletion

Cannot have received: other organ transplant

subjects who have undergone other organ transplants

Cannot have received: anti-tumor drug treatment

Exception: within 4 weeks before lymphodepletion or within 5 half-lives (whichever is shorter)

Received anti-tumor drug treatment or participated in other interventional clinical studies within 4 weeks before lymphodepletion or within 5 half-lives (whichever is shorter), including but not limited to chemotherapy drugs, small molecule targeted drugs, monoclonal antibodies, antibody-drug conjugates, etc.

Lab requirements

Blood counts

Hemoglobin (Hb) ≥80 g/L, ANC ≥1×10^9/L, Platelet Count (PLT) ≥50×10^9/L

Kidney function

Serum creatinine ≤1.5×ULN, or creatinine clearance ≥50 mL/min (Cockcroft-Gault)

Liver function

Total bilirubin ≤1.5×ULN (≤3×ULN for subjects with liver lesions or Gilbert's syndrome); ALT and AST ≤3×ULN (≤5×ULN for subjects with liver lesions)

Cardiac function

QTcF ≤450 ms (males), ≤470 ms (females); LVEF ≥50%; NYHA <II; no serious arrhythmias, acute coronary syndrome, or grade 3+ cardiovascular/cerebrovascular events within 6 months; controlled blood pressure

Hematological parameters...Coagulation function...Hepatic, renal, and pulmonary function must meet the following requirements

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Could you qualify for this trial?

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

Check if I qualify