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OncoMatch/Clinical Trials/NCT06690827

Clinical Trial of CD123-targeted CAR-NK Therapy for Relapse/refractory AML or BPDCN

Is NCT06690827 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies Anti-CD123 CAR NK cells for aml (acute myeloid leukemia).

Phase 1RecruitingChongqing Precision Biotech Co., LtdNCT06690827Data as of Jun 2026Location: China

Treatment: Anti-CD123 CAR NK cellsThis is a clincal trial initiated by investigator to evaluate the safety and efficacy of anti-CD123 CAR-NK in the treatment of patients with relapsed/refractory acute myeloid leukemia or blastic plasma cell like dendritic cell tumors.

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Extracted eligibility criteria

Treatments studied

Other

Anti-CD123 CAR NK cells

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Required: IL3RA positive expression (positive)

Performance status

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

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: chemotherapy

Exception: except for those who have confirmed disease progression after treatment

Receipt of anti-tumor therapies prior to screening, including chemotherapy, targeted therapy, or other experimental drug treatments within 14 days or at least 5 half-lives (whichever is shorter), except for those who have confirmed disease progression after treatment

Cannot have received: targeted therapy

Exception: except for those who have confirmed disease progression after treatment

Receipt of anti-tumor therapies prior to screening, including chemotherapy, targeted therapy, or other experimental drug treatments within 14 days or at least 5 half-lives (whichever is shorter), except for those who have confirmed disease progression after treatment

Cannot have received: other experimental drug treatments

Exception: except for those who have confirmed disease progression after treatment

Receipt of anti-tumor therapies prior to screening, including chemotherapy, targeted therapy, or other experimental drug treatments within 14 days or at least 5 half-lives (whichever is shorter), except for those who have confirmed disease progression after treatment

Lab requirements

Blood counts

white blood cells >1.0×10^9/l, neutrophils >0.5×10^9/l, lymphocytes >0.5×10^9/l, platelets >50×10^9/l

Kidney function

serum creatinine ≤2.0×uln

Liver function

alt and ast ≤3.0×uln (for patients with liver invasion ≤5.0×uln); total bilirubin ≤2.0×uln (for patients with gilbert's syndrome ≤3.0×uln)

Cardiac function

echocardiography indicates a left ventricular ejection fraction ≥50%, and no significant abnormalities on electrocardiogram

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

Frequently asked questions

Is NCT06690827 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, targeted therapy, other experimental drug treatments disqualifies patients from enrollment.

Does this trial require IL3RA?

Yes, IL3RA positive expression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 75 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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