OncoMatch

OncoMatch/Clinical Trials/NCT07480954

Dual-Targeting CAR-NK Cells for Recurrent Ovarian Cancer (MSLN, FRα, MUC16)

Is NCT07480954 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Dual-target CAR-NK cell product and Lymphodepleting chemotherapy for epithelial ovarian cancer.

Phase 1/2RecruitingBeijing BiotechNCT07480954Data as of May 2026

Treatment: Dual-target CAR-NK cell product · Lymphodepleting chemotherapyThis Phase 1/2 study evaluates the safety, tolerability, and preliminary anti-tumor activity of dual-targeting chimeric antigen receptor natural killer (CAR-NK) cells in participants with recurrent or refractory epithelial ovarian, primary peritoneal, or fallopian tube cancer. At screening, each participant's tumor is assessed for expression of Mesothelin (MSLN), Folate Receptor alpha (FRalpha/FOLR1), and MUC16 (CA 125). Participants are assigned to the dual-target CAR-NK product that best matches their tumor antigen profile to reduce the risk of antigen escape.

Check if I qualify

Extracted eligibility criteria

Cancer type

Ovarian Cancer

Biomarker criteria

Required: MSLN overexpression above protocol-defined threshold (protocol-defined threshold)

Tumor expresses at least two of the following targets above protocol-defined threshold: MSLN, FRalpha (FOLR1), MUC16 (CA 125)

Required: FOLR1 overexpression above protocol-defined threshold (protocol-defined threshold)

Tumor expresses at least two of the following targets above protocol-defined threshold: MSLN, FRalpha (FOLR1), MUC16 (CA 125)

Required: MUC16 overexpression above protocol-defined threshold (protocol-defined threshold)

Tumor expresses at least two of the following targets above protocol-defined threshold: MSLN, FRalpha (FOLR1), MUC16 (CA 125)

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: platinum-based chemotherapy

Cannot have received: gene-modified cellular therapy (car-t, car-nk)

Exception: within 6 months (or any prior therapy directed to the same target, per protocol)

Lab requirements

Blood counts

anc >= 1.0 x 10^9/l; platelets >= 75 x 10^9/l; hemoglobin >= 8 g/dl

Kidney function

creatinine clearance >= 50 ml/min

Liver function

ast/alt <= 3 x uln (<= 5 x uln with liver metastases); total bilirubin <= 1.5 x uln

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