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NCT Number: NCT07018453

A Study Comparing SHR-3167 and Insulin Degludec in Type 2 Diabetic Subjects Treated With Basal Insulin With or Without Oral Antidiabetic Drugs

The purpose of this study is to evaluate the glycemic control and safety of SHR-3167 and Insulin Degludec in type 2 diabetic participants treated with basal insulin with or without oral antidiabetic drugs.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital of Chongqing Medical University, Chongqing, Chongqing Municipality, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and females, 18 - 65 years old at the time of signing informed consent.
  • Diagnosed with type 2 diabetes mellitus (T2DM) for at least 6 months prior to the day of screening.
  • Treatment with basal insulin with or without oral antidiabetic drugs at least 90 days prior to the day of screening.
  • 6.5% ≤ HbA1c ≤ 10.0% at screening.

Exclusion criteria

  • Uncontrollable hypertension (with or without antihypertensive treatment) : systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg at screening.
  • Diagnosed or suspected with type 1 diabetes mellitus, latent autoimmune diabetes mellitus in adult (LADA), other special types of diabetes or secondary diabetes.
  • Known or suspected allergy or intolerance to the test drug or excipient.
  • There was a history of diabetic ketoacidosis or hyperglycemic hyperosmolar state within the previous 6 months.
  • There is acute or chronic hepatitis, liver cirrhosis, or a history of other serious liver diseases other than non-alcoholic fatty liver disease.
  • There is hyperthyroidism or hypothyroidism requiring treatment.
  • Malignancy within 5 years prior to screening or high risk of recurrence.
  • Those who have a history of severe cardiovascular and cerebrovascular diseases within 6 months before screening.
  • Participated in clinical trials of any drug or medical device within 3 months prior to screening.

Treatment and study plan

SHR-3167

Drug

SHR-3167 Injection.

insulin degludec

Drug

Insulin Degludec Injection.

Primary outcomes

  1. Change in glycosylated hemoglobin (HbA1c) from baseline.

    Time frame: 16 weeks.

Secondary outcomes

  1. Proportion of subjects with glycosylated hemoglobin (HbA1c) < 7.0% from baseline.

    Time frame: 16 weeks.

  2. Change in fasting plasma glucose (FPG) from baseline.

    Time frame: 16 weeks.

  3. Change in self-measured (capillary) blood glucose (SMBG) from baseline.

    Time frame: 16 weeks.

Sponsors and collaborators

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Industry

Registry information

Official study title

A Randomized, Open-label, Treat-to-target, Parallel-Controlled Phase II Clinical Study Investigating the Efficacy and Safety of SHR-3167 and Insulin Degludec in Type 2 Diabetic Subjects Treated With Basal Insulin With or Without Oral Antidiabetic Drugs

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 12, 2025
Registry last updated
Nov 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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