Comparing the Efficacy and Safety Between Continuous Subcutaneous Beinaglutide and CSII for Newly Diagnosed T2DM Patients

Launched by BEIJING HOSPITAL · Jun 13, 2019

Keywords

ClinConnect Summary

This clinical trial is studying two different ways to manage type 2 diabetes in adults who have recently been diagnosed. Specifically, it will compare the effectiveness and safety of a medication called Beinaglutide that is given continuously under the skin, to a traditional method known as continuous subcutaneous insulin infusion (CSII). The goal is to see which method helps control diabetes better and is safer for patients.

To be eligible for this trial, participants must be between 18 and 70 years old, newly diagnosed with type 2 diabetes (within the last year), and have specific blood sugar levels and body weight. People who have other types of diabetes, serious health issues, or certain medical histories may not qualify. Those who join the study can expect to receive careful monitoring and support from the research team. It’s important to note that participants will need to use effective contraception if they have the potential to become pregnant during the study. Overall, this trial aims to improve diabetes management options for newly diagnosed patients.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Age 18 to 70 years (inclusive) at enrollment, regardless of gender.
• • 2. Voluntary signing of the informed consent form.
• • 3. Newly diagnosed type 2 diabetes mellitus patients, diagnosed according to the WHO 1999 criteria, with a disease duration ≤1 year.
• • 4. HbA1c between 7.5% and 10.0%.
• • 5. BMI between 24 kg/m² and 42 kg/m².
• • 6. Subjects who have not taken antidiabetic medications or have used oral antidiabetic medications for less than 3 months and have discontinued for more than 1 month (calculated from the date of signing the informed consent form).
• • 7. Subjects with reproductive potential (including male subjects whose partners have reproductive potential) agree to use effective contraception during the study and for 1 month after study completion.
• Exclusion Criteria:
• • 1. Patients with type 1 diabetes or other types of diabetes.
• • 2. History of obstructive intestinal diseases or potential complications: subjects with post-abdominal surgery or peritoneal infection-related intestinal adhesions, intestinal obstruction sequelae; subjects with intestinal motility disorders, chronic constipation; subjects with a history of Crohn's disease or ulcerative colitis.
• • 3. History of pancreatitis.
• • 4. Family history of medullary thyroid carcinoma.
• • 5. History of malignant tumors.
• • 6. ALT, AST \>3 times the upper limit of normal, and/or total bilirubin \>2 times the upper limit of normal.
• • 7. Moderate to severe renal insufficiency (eGFR \<60 ml/min/1.73m²).
• • 8. Triglycerides ≥5.0 mmol/L.
• • 9. Multiple endocrine neoplasia type 2 (MEN 2).
• • 10. Participation in any pre-marketing drug study within 3 months.
• • 11. Use or expected use of systemic corticosteroids, immunosuppressants, or cytotoxic drugs during the study period.
• • 12. History of diabetic ketoacidosis or non-ketotic hyperosmolar coma within 6 months prior to screening.
• • 13. Blood pressure exceeding the following criteria (untreated or treated): systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg.
• • 14. History of any of the following cardiovascular diseases within 3 months prior to screening: acute myocardial infarction, New York Heart Association functional class III/IV heart failure or left ventricular ejection fraction ≤40%, or cerebrovascular event (stroke).
• • 15. Allergy to binaclotide or any component of the study drug, or allergy to insulin or any component of the insulin used in the study.
• • 16. Presence of other severe diseases that may interfere with the study, as judged by the investigator.
• • 17. Pregnant or breastfeeding women.
• • 18. Poor compliance, as judged by the investigator, and inability to complete the study as required.
• • 19. Inability to undergo continuous pump infusion: subjects allergic to subcutaneous infusion tubes or adhesive tape; subjects unwilling to have long-term subcutaneous infusion tubes or continuous pump use; subjects with psychological aversion to pump therapy; subjects or their families lack relevant knowledge and are unable to master the use after training; subjects with severe psychological disorders or mental abnormalities; subjects who are unable to care for themselves and have no caregivers.
• • 20. Any other factors deemed unsuitable for participation in the study by the investigator.