Clinical Research Directory

Inclusion Criteria: 1. Age ≥ 55 and ≤ 85 on the date of signing the informed consent, males or females; 2. BMI ≥ 19 kg/m2 and ≤ 32 kg/m2, weight ≥ 45 kg and ≤ 100 kg at screening or baseline; 3. Must meet the diagnostic criteria for MCI due to AD or mild AD; 4. The total score of HAMD-17 should be ≤ 10 scores at screening and baseline; 5. The score of Hachinski ischemic scale should be ≤ 4 scores at screening and baseline; 6. Qualitative amyloid PET scan results from the central laboratory confirmed the presence of pathological changes in AD; 7. Agreed to test ApoE genotype; 8. Have a stable caregiver; where symptomatic drugs for AD is used, they must be stable for at least 3 months prior to the baseline visit. Exclusion Criteria: 1. Cognitive impairment of subjects due to other medical or neurological factors (other than AD); 2. History of stroke or transient ischemic attack, seizures, or other unexplained loss of consciousness within the past year; 3. Any psychiatric diagnosis that may interfere with the subject's cognitive assessment; 4. Cannot tolerate MRI or has contraindications to MRI, has significant lesions shown on MRI during screening, or has other conditions that the investigator believes may bring a significant risk to the subject; 5. Suspected allergy to Aβ antibody drugs and excipients; 6. Patients who had severe trauma or had undergone surgery within 6 months prior to screening, or were scheduled to undergo surgery during the trial; 7. History of moderate (3b) or severe renal failure or insufficiency; 8. Uncontrolled hypertension: systolic blood pressure \> 160 mmHg and diastolic blood pressure \>100 mmHg in supine position during screening or baseline; 9. 12-lead ECG showed QTcF \> 450ms for male and \> 470ms for female during screening; 10. History of hypoglycemic coma or uncontrolled diabetes 6 months prior to the screening period; 11. Thyroid dysfunction; 12. Had unstable or clinically significant cardiovascular disease within 1 year prior to the screening period, had or currently has atrial fibrillation; 13. History of malignancy within 5 years prior to screening; 14. Patients with clinically significant systemic immunosuppression due to the persistent effects of immunosuppressive drugs; 15. Human immunodeficiency virus antibody (HIV-Ab), treponema pallidum antibody and hepatitis C virus antibody (HCV-Ab) were positive during screening. Hepatitis B active subjects (Hepatitis B virus surface antigen (HBsAg) positive with HBV DNA \> upper limit of normal); 16. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) exceeding 3 times ULN, or total bilirubin exceeding 2 times ULN; 17. Folic acid or vitamin B12 below the lower limit of normal; 18. coagulation disorders; 19. According to the investigators, the subjects were suicidal or had committed suicidal behavior in the six months before the screening period; 20. Severe visual or hearing impairment, unable to cooperate with the completion of the scale; 21. A woman who is pregnant, or a woman of childbearing potential whose pregnancy test results are positive, or who is breastfeeding; or has a plan to have a child, unwilling or unable to take effective contraceptive measures within 30 days prior to the screening period or six months after the last use of the investigational drug; 22. History of drug abuse or addiction; 23. Three months prior to the randomization period or planned to use dual antiplatelet or anticoagulant drugs during the trial; 24. Received any passive immunotherapy or other long-acting biologics used to prevent or delay cognitive decline within 1 year prior to screening; 25. Investigators and relevant staff of the research Centre or others directly involved in programme implementation; 26. The investigator considers that there are any circumstances that would cause the subject to be unable to complete the study or pose a significant risk to the subject or other factors that would interfere with the subject's ability to complete the study evaluation.