A Trial Investigating the Efficacy and Safety of Insulin Degludec/Liraglutide Injection in Subjects With Type 2 Diabetes

Phase 3

Not yet recruiting

• Conditions: Type 2 Diabetes
• Interventions: Drug: Insulin Degludec/liraglutide Injection; Drug: XULTOPHY®

• Registration Number: NCT06559722
• Lead Sponsor: Tonghua Dongbao Pharmaceutical Co.,Ltd

Brief Summary

This is a randomised, open-label, multicenter, active-controlled, parallel-design, phase III clinical trial. The purpose of this study to compare the efficacy and safety of Insulin Degludec/Liraglutide Injection with XULTOPHY® once daily via subcutaneous injection in Chinese Subjects with Type 2 Diabetes.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-08
• Study Start: 2024-08
• Study First Submitted: 2024-08-14
• Study First Submitted QC: 2024-08-15
• Last Update Submitted: 2024-08-15
• Study First Posted: 2024-08-19
• Last Update Posted: 2024-08-19
• Primary Completion: 2025-10
• Study Completion: 2026-02

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 510

Inclusion Criteria

• Subjects who voluntarily participate in this clinical trial and signed the informed consent form (ICF);

• Chinese subjects aged 18-75 years (both inclusive) at the time of consent, male or female;

• Type 2 diabetes mellitus (clinically diagnosed for more than 6 months);

• HbA1c7.0-10.0 % (both inclusive) by central laboratory analysis at the time of screening;

• Current treatment for at least 90 calendar days prior to screening with metformin monotherapy or metformin in any combination with 1 additional OADs (including fixed combination): SU, glinides, AGI, SGLT2i or TZD. For ≥ 60 calendar days prior to screening subjects should be on a stable dose of:

  1. Metformin (≥ 1500 mg or at maximum tolerated dose) or
  2. Metformin (≥1500 mg or max tolerated dose) and SU (≥half of the max approved dose according to local label) or
  3. Metformin (≥1500 mg or max tolerated dose) and glinides (≥half of the max approved dose according to local label) or
  4. Metformin (≥1500 mg or max tolerated dose) and AGI (≥half of the max approved dose according to local label) or
  5. Metformin (≥1500 mg or max tolerated dose) and SGLT2i (≥half of the max approved dose or minimum maintenance dose such as empagliflozin 10 mg and canagliflozin 100 mg according to local label) or
  6. Metformin (≥1500 mg or max tolerated dose) and TZD (≥half of the max approved dose according to local label);

• Body mass index (BMI) ≥ 19.0 kg/m2 and ≤ 40 kg/m2;

• Able and willing to adhere to the protocol including performing self-monitoring of plasma glucose profiles, keeping a trial diary and using a pre-filled pen device.

Exclusion Criteria

Subjects who meet any of the following criteria will be excluded from the study:

• Subjects with diabetes of other types than T2DM;
• Known or suspected hypersensitivity to trial product(s) or related components;
• Participated in any clinical trial and Receipt of any treatment of investigational medicinal product (IMP) or medical device within 90 days prior screening;
• Treatment with glucose lowering agent(s) other than stated in the inclusion criteria 5 for cumulatively more than 14 days in a period of 90 days before screening; or treatment with these agent(s) in a period of 30 days before screening and might influence the assessment of efficacy of glycemic control (Judged by the investigator);
• Treatment with systemic corticosteroid for cumulatively more than 14 days in a period of 90 days before screening (including intravenous, muscle and subcutaneous injections, and oral administration, except for local, intraocular, nasal, intraarticular, and inhalation medications); or treatment with these agent(s) in a period of 30 days before screening and might influence the assessment of efficacy (Judged by the investigator);
• Treatment with glucose lowering agent(s) of herbal traditional Chinese medicine or other local herbal medicines for cumulatively more than 14 days in a period of 90 days before screening; or treatment with these agent(s) in a period of 30 days before screening and might influence the assessment of efficacy (Judged by the investigator);
• Treated with stable insulin regimen (except for short-term treatment (e.g., no more than 14 days of continuous treatment)), or treatment with insulin in a period of 30 days before screening and might influence the assessment of efficacy (Judged by the investigator);
• Treatment with GLP-1 receptor agonists or DPP-4 inhibitors within 90 calendar days prior to screening;
• Impaired liver function, defined as aspart aminotransferase (AST) or alanine aminotransferase (ALT) ≥ 2.5 times upper limit of the normal or a total bilirubin level (TBIL) ≥ 1.5 times upper limit of the normal;
• Triglycerides >5.6 mmol/L at screening;
• Impaired renal function, defined as creatinine clearance (Ccr) of less than 60 mL/min (calculated from the Cockcroft-Gault formula);
• Have had 1 or more episodes of severe hypoglycemia within the 6 months prior to screening.
• Have had 1 or more episodes of acute diabetic complications (diabetic ketoacidosis, hyperglycemic hyperosmolar state, diabetic lactic acidosis, etc.) within the 6 months prior to screening.
• With concomitant conditions at screening that may affect the evaluation of the study, including cardiovascular and cerebrovascular diseases, respiratory diseases, gastrointestinal diseases, liver diseases, kidney diseases, nervous system diseases, psychiatric diseases, hematological diseases, immune system diseases, endocrine system diseases, pancreatic diseases, and/or malignant tumors.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Insulin Degludec/liraglutide injection	Insulin Degludec/liraglutide Injection	Subcutaneously (s.c., under the skin) administration once daily in combination with metformin. Dose was individually adjusted.
XULTOPHY®	XULTOPHY®	Subcutaneously (s.c., under the skin)administration once daily in combination with metformin. Dose was individually adjusted.

Primary Outcome Measures

Name	Time	Method
Change from baseline in HbA1c after 26 weeks of treatment	Baseline, Week 26	Calculated based on HbA1c level measured in plasma

Secondary Outcome Measures

Name	Time	Method
Change from baseline in body weight after 12, 26 weeks of treatment	Baseline, Week 12, Week 26	Calculated based on body weight measurement
Number of treatment emergent adverse events	From Baseline to Week 27	Count
Change from baseline in 7-point SMBG values after 12, 26 weeks of treatment	Baseline, Week 12, Week 26	Calculated based on 7-point SMBG values
Changes from baseline in fasting plasma glucose (FPG) after 12, 26 weeks of treatment	Baseline, Week 12, Week 26	Calculated based on FPG level measured in plasma
Proportion of subjects that achieved HbA1c<7% after 12, 26 weeks of treatment	Week 12, Week 26	Calculated based on HbA1c level measured in plasma
Proportion of subjects that achieved HbA 1c ≤ 6.5% after 12, 26 weeks of treatment	Week 12, Week 26	Calculated based on HbA1c level measured in plasma
Number of treatment emergent hypoglycaemic episodes	From Baseline to Week 27	Count
Incidence of anti-drug antibodies (ADA), and neutralising antibodies (if applicable)	Baseline, Week 12, 26, and 27 (if applicable)	Calculated based on the values of anti-drug antibodies (ADA), and neutralising antibodies (if applicable)
Number of participants with injection site reactions	From Baseline to Week 27	Count (spontaneous pain, tenderness, itching, redness, edema, induration/infiltration)
Plasma concentrations of degludec, liraglutide	Baseline, Week 2, 6, 12, 20, 26	Calculated based on plasma concentrations of degludec, liraglutide