1\. Signed the informed consent form (ICF) before the trial, fully understanding the trial content, process and possible adverse reactions, and being able to comply with the contraindications and restrictions specified in this protocol.
2.At the age of 18-75 (inclusive) at the time of informed consent, male or female.
3.Negative pregnancy test results for serum human chorionic gonadotropin (HCG) in women of childbearing potential at screening.
4.Diagnosed with type 2 diabetes mellitus above or equal to 6 months.
You may not be if
1.Presence or history of malignant neoplasm prior to screening.
2.Known or suspected hypersensitivity to investigational medical product(s) or related products.
3.Severe hypoglycemia (Level 3 hypoglycemia) within 6 months prior to screening.
4.History of acute heart failure within 6 months prior to screening or hospitalization for coronary heart disease, myocardial infarction, unstable angina, stroke within 6 months prior to screening.
5\. Participated in another interventional clinical study within 4 weeks prior to randomization.
