A Trial Comparing HR17031 With Insulin Glargine in Patients With Type 2 Diabetes

NCT06871761 | Completed Phase 3

• 1 other identifier: HR17031-302
• Study Type: interventional
• Target: 393
• Locations: 1 country
• Sites: 1

Brief Summary

To compare the efficacy and safety of HR17031 injection and insulin glargine, including the changes of efficacy indicators such as HbA1c, fasting blood glucose, body weight and safety indicators such as adverse events and hypoglycemic events.

Conditions

Adult Patients With Type 2 Diabetes

Outcome Measures

Primary Outcomes (1)

• Changes in HbA1c from baseline to week 26

  from baseline to week 26

Secondary Outcomes (8)

• Proportion of subjects achieved HbA1c<7.0% at week 26

  at week 26

• Change in body weight from baseline to week 26

  from baseline to week 26

• Proportion of subjects achieved HbA1c<7.0% and no weight gain at week 26

  at week 26

• Daily Insulin dose at week 26

  at week 26

• The proportion of subjects achieved HbA1c≤6.5% at week 26

  at week 26

Study Arms (2)

Treatment group A: HR17031 injection

EXPERIMENTAL

Drug: HR17031 injection

Treatment group B: insulin glargine

ACTIVE COMPARATOR

Drug: insulin glargine

Interventions

HR17031 injection DRUG

HR17031 injection

Treatment group A: HR17031 injection

insulin glargine DRUG

insulin glargine

Treatment group B: insulin glargine

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female, aged 18-75 years at the time of signing the informed consent (both ends included)
• Body Mass index (BMI) of 20.0-40.0 kg/m2 (both ends included)
• Diagnosed with type 2 diabetes for at least 90 days prior to screening
• Tested by local laboratory, HbA1c is 7.5%-10.5% (including both ends)
• Before screening, the daily basal insulin dose had been stabilized at 20-40U/ day (including both ends) for at least 60 days
• Stable treatment with metformin alone or in combination with another OAD for ≥60 days prior to screening. Metformin dose ≥1500 mg/ day or maximum tolerated dose.
• Ability and willingness to comply with protocol requirements, including self-monitoring of blood glucose, recording subject diary, and using pre-filled injection pen.

You may not qualify if:

• Known or suspected allergy to the investigational drug product or its components or excipients;
• Systemic glucocorticoid use within 3 months prior to screening
• Use of weight loss drugs within 3 months prior to screening
• Insulin therapy other than basal insulin was used within 3 months prior to screening
• Cardiovascular disease, defined as congestive heart failure (NYHA III-IV), unstable angina pectoris, stroke (except lacunar infarction without symptoms), myocardial infarction, coronary revascularization within 6 months prior to screening; And/or coronary, carotid, or peripheral arterial revascularization is planned at screening
• (with or without treatment) uncontrolled severe hypertension (systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg)
• Proliferative retinopathy or macular degeneration requiring acute treatment, painful diabetic neuropathy, diabetic foot ulcers, intermittent claudication at screening;
• Patients diagnosed with mental disorders; Mentally incapacitated or speech impediment, unable to fully understand the trial protocol or unwilling to collaborate;
• Known or suspected abuse of alcohol or narcotics;
• Previous history of pancreatitis (acute or chronic)
• During pregnancy or lactation;fertile women (WOCBP) or men who have fertility plan or unwilling to use appropriate contraceptive methods from the signing of the informed consent to 3 months after last use of the investigational drug product;
• Any condition, determined by the investigator, interfere with the efficacy or safety results of the trial.

Sponsors & Collaborators

• Jiangsu HengRui Medicine Co., Ltd.: lead

Study Sites (1)

Shanghai Zhu Xianyi Memorial Hospital, Tianjin Medical University

Tianjin, Tianjin Municipality, 300400, China

Location

MeSH Terms

Interventions

Insulin Glargine

Intervention Hierarchy (Ancestors)

Insulin, Long-Acting; Insulins; Pancreatic Hormones; Peptide Hormones; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Peptides; Amino Acids, Peptides, and Proteins

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 26, 2025
• First Posted: March 12, 2025
• Study Start: May 8, 2024
• Primary Completion: May 13, 2025
• Study Completion: May 13, 2025
• Last Updated: January 13, 2026

Record last verified: 2025-02

Locations

CN (1)