Study to Evaluate the Safety and Preliminary Efficacy of CLL1 and CD38 Dual CAR-T in r/r AML

Inclusion Criteria:

1. 18-70 years old (including the critical value) when signing the informed consentform;

2. Diagnosed with acute myeloid leukemia (excluding APL) according to the World HealthOrganization 2016 criteria and relapsed and refractory AML according to the ELN2022criteria;

3. Positive expression of CLL1 and/or CD38 in malignant cells must be detected byimmunohistochemistry or flow cytometry (≥20 % );

4. If there are AEs caused by previous chemotherapy, it must be restored to CTCAE V5.0grade 1;

5. Estimated survival time ≥3 months;

6. ECOG score 0 or 1 during screening period;

7. Hemoglobin ≥80g/L (have not received red blood cell transfusion within 7 days beforescreening, use of recombinant human erythropoietin is allowed);

8. Adequate organ functional reserve:

9. Alanine aminotransferase/aspartate aminotransferase ≤2.5× ULN (upper limit ofnormal value);

10. Serum total bilirubin ≤2× ULN, except for subjects with congenitalbilirubinemia (for subjects with Gilbert syndrome, direct bilirubin needs to be ≤1.5× ULN);

11. Serum creatinine clearance >45mL/min (calculated according to theCockcroft-Gault formula);

12. Left ventricular ejection fraction ≥35%;

13. Basic oxygen saturation in indoor air environment is ≥ 92 %

14. Ability to discontinue corticosteroids (dexamethasone ≥3 mg/day or other equivalentdoses of steroids) starting on day -7 and continuing until 30 days after CAR-T cellinfusion;

15. Women of childbearing age must have a negative pregnancy test for human chorionicgonadotropin (HCG) (immunofluorescence method) during the screening period andbaseline period. Male subjects will need to agree not to donate sperm for at leastone year after reinfusion. Males and sexual partners of childbearing potential agreeto use highly effective contraceptive measures for at least 1 year after infusion;

16. Agree to perform follow-ups in accordance with the requirements of the protocol andinformed consent form;

17. With the consent of the subject and the informed consent form voluntarily signed bythe subject or his legal representative.

Exclusion Criteria:

1. Diagnosis of acute promyelocytic leukemia;

2. clinical trial investigational drugs or cell therapies within 2 weeks or 5half-lives ;

3. Acute myeloid leukemia of unknown lineage ;

4. Those who have active graft-versus-host disease (GVHD) at the time of enrollment ordevelop active acute or chronic GVHD within 4 weeks after enrollment or requireimmunosuppressive drugs to treat GVHD;

5. There is an active infection;

6. Suffering from other malignant tumors (except non-melanoma skin cancer and in situcervical cancer, bladder cancer, and breast cancer with a disease-free survivalperiod of more than 5 years);

7. The subject has had a stroke or epilepsy within 6 months before signing the informedconsent form;

8. The subjects' cardiac function showed the following conditions:

9. New York Heart Association (NYHA) class III or IV heart failure;

10. Myocardial infarction or coronary artery bypass grafting (CABG) occurred within 6 months before signing the informed consent form;

11. A history of clinically significant ventricular arrhythmia or syncope ofunknown origin (not caused by vasovagal or dehydration);

12. Have a history of severe non-ischemic cardiomyopathy;

13. Cardiac dysfunction (left ventricular <35%) assessed by echocardiography ormultiple gated acquisition scans, or other heart disease with clinical symptomswithin 6 months before enrollment;

14. Active or previous central nervous system involvement, or clinically significantclinical manifestations of central nervous system involvement in subjects with acutemyeloid leukemia ;

15. A positive virological test result for any of the following:

16. Human immunodeficiency virus antibodies (HIV antibodies);

17. Hepatitis C virus antibody (HCV antibody), those who are positive need to betested for HCV-RNA, and those whose values are lower than the lower limit ofthe detection value can be enrolled;

18. HBsAg positive; or HBcAb positive; if HBcAb is positive, further testing of HBVDNA copy number is required . Those who are lower than the lower limit of thedetection value can be enrolled;

19. Treponema pallidum antibodies (TPPA antibodies);

20. presence of pulmonary fibrosis;

21. Severe allergic history or allergic constitution;

22. The subject has undergone open injury or major surgery (referring to level IIIsurgery and level IV surgery) within 2 weeks before signing the informed consentform, or plans to have surgery during the trial or within 2 weeks after reinfusion (excluding local anesthesia surgery) ;

23. for cyclophosphamide combined with fludarabine ;

24. Cannulae or drains other than central venous catheters;

25. Pregnant women, lactating women, or men who plan to give birth within 1 year ofreceiving treatment;

26. Any other circumstances that the researcher deems inappropriate for inclusion.