A Study of TG103 Injection Monotherapy in Treatment of Type 2 Diabetes Mellitus

Prior treatment

• 2\. Body weight change more than 5% within 1 month prior to screening;
• 3\. Received any of the following medications:
  • Prior discontinuation of DPP-4 inhibitors or GLP-1 receptor agonists for efficacy, tolerability, and safety reasons;
  • Systemic glucocorticoid and growth hormone have been used within 8 weeks before screening;
• 4\. History of ≥2 episodes of grade 3 hypoglycemia within 6 months prior to screening, or grade 3 hypoglycemia between screening to randomization;
• 5\. Acute complications of diabetes, such as diabetic ketoacidosis and hyperglycemic hyperosmolar status, occurred ≥1 time within 6 months prior to screening;
• 6\. Severe chronic complications of diabetes (e.g., proliferative diabetic retinopathy, severe diabetic neuropathy, diabetic foot, etc.) within 6 months prior to screening
• 7\. History of acute or chronic pancreatitis prior to screening;
• 8\. Subjects with clinically significant gastric emptying abnormalities (e.g., gastric outlet obstruction), severe chronic gastrointestinal diseases (e.g., gastroparesis, inflammatory bowel disease, or intestinal obstruction) within 6 months prior to screening, or who have undergone gastrointestinal surgery that affects gastric emptying;
• 10\. Hemorrhagic stroke or acute ischemic stroke disease occurred within 6 months prior to screening;
• 12\. Any type of malignant tumor treated or untreated within 5 years prior to screening (except for clinically cured basal cell carcinoma or carcinoma in situ);
• 13\. Severe or acute infection within 4 weeks prior to screening, or refractory urinary tract or genital infection within 6 months prior to screening;
• 15\. Subjects with thyroid dysfunction that cannot be controlled by a stable drug dose at screening, or with clinically significant abnormalities in thyroid function examination results requiring drug treatment at screening;
• 19\. Subjects who have lost more than 400 mL blood due to blood donation or other reasons within 3 months prior to screening;
• 20\. Average alcohol intake more than 21 units of alcohol (male)/14 units of alcohol (female) per week within the 3 months prior to screening (1 unit ≈360 mL beer, or 45 mL spirits with 40% alcohol content, or 150 mL wine);
• 21\. Subject participated in any drug or medical device clinical study within 3 months prior to screening (except for screening failure);

Other illness

• 1\. Type 1 diabetes;
• 11\. History of psychiatric diseases (such as depression, anxiety, etc.) during screening; or symptomatic gallbladder disease; or history of other diseases that may endanger the safety of the subject and that the investigator deems inappropriate for enrollment;
• 14\. Having a significant blood system disease (e.g., aplastic anemia, myelodysplastic syndrome) or any disease causing hemolysis or red blood cell instability (e.g., malaria) at screening;
• 16\. Personal or family history of medullary thyroid cancer (MTC) or type 2 multiple endocrine tumor syndrome at screening;
• iii. Serological examination:
  • Human immunodeficiency virus antibody or treponema pallidum antibody is positive;
  • Hepatitis C antibody is positive, and HCV RNA was higher than the lower limit of the detection reference range;
  • Hepatitis B surface antigen is positive, and the quantitative detection result of HBV DNA was higher than the lower limit of the detection reference range;
• 18\. Known allergy to the test drug, Empagliflozin, or related excipients;

Lab values

• 9\. Any of the following cardiovascular events within 6 months prior to screening: decompensated cardiac insufficiency (NYHA class III or IV); history of unstable angina pectoris, myocardial infarction, coronary artery bypass grafting, or coronary stent implantation; long QT syndrome or prolonged QTcF interval (QTcF: male \>450 ms, female \>470 ms) on 12-lead ECG; severe arrhythmias that are evaluated by the investigator to be inappropriate for participation in this clinical trial;
• ii. Laboratory tests show any of the following abnormalities:
  • FPG≥13.9 mmol/L;
  • ALT or AST≥2.5×ULN;
  • Total bilirubin (TBiL) ≥2.0×ULN;
  • Triglyceride \>5.7 mmol/L;
  • eGFR\<45 mL/(min\*1.73 m\^2);
  • Serum amylase and/or lipase ≥3×ULN;
  • Hemoglobin \<100 g/L;
  • Calcitonin≥50 ng/L(pg/mL);

Other

• 17\. Any of the indicators meet the following criteria:
• i. Systolic blood pressure ≥ 160mmHg or diastolic blood pressure ≥ 100mmHg at screening or before randomization;
• 22\. Pregnant or lactating female;
• 23\. Not suitable for this study in the investigator's opinion.

• 1.Subjects have diagnosed with type 2 diabetes according to the Guidelines for prevention and treatment of type 2 diabetes in China (2020 Edition), and have been diagnosed with T2DM for at least 8 weeks before screening;
• 2.Aged 18 to 75 years (inclusive), no gender limitation;
• 3\. Body Mass Index (BMI): 18.5≤BMI≤40;
• 4\. No hypoglycemic drugs have been used within 8 weeks before screening, and the blood glucose control is poor after diet and exercise therapy alone
• 5.The continuous use of insulin ≤14 days (except gestational diabetes), and/or the types of hypoglycemic drugs used in combination \<3 with the continuous use time ≤4 weeks within 1 year (more than 8 weeks) before screening;
• 6.HbA1c must meet the following criteria:
  • Screening: 7.5% ≤ HbA1c ≤ 11.0% (Local laboratory)
  • Baseline: 7.0% ≤ HbA1c ≤ 10.5% (Central laboratory)
• 7.Subjects of childbearing potential must use reliable methods of contraception throughout the study period and at least 3 months after the last dose to avoid pregnancy in female subjects or pregnancy in the male subject's partner;
• 8\. Willing and able to accurately use home glucose meter for self-glucose monitoring;
• 9\. Be able to understand and follow the trial procedure, voluntarily participate in the trial and sign the informed consent form.