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NCT Number: NCT06778967

A Phase III Clinical Study to Evaluate the Efficacy and Safety of GZR18 Injection in Adult Type 2 Diabetes Mellitus

The main purpose of this study is to investigate the Efficacy and Safety of GZR18 Injection in Chinese Subjects with Type 2 Diabetes Mellitus and Poor Blood Glucose Control by Metformin Monotherapy or in Combination with Sodium-dependent Glucose Transporter 2 (SGLT2) Inhibitors or Sulfonylureas

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Tianjin Medical University General Hospital

Tianjin, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • T2DM is diagnosed for at least 12 weeks according to the diagnostic criteria of diabetes mellitus issued by the World Health Organization (WHO) in 1999 and the supplementary diagnostic criteria of WHO in 2011 (HbA1c diagnosis is recommended).
  • Antidiabetic drugs that meet any of the following within 8 weeks before screening:
  • A stable dose of metformin hydrochloride monotherapy at a dose of ≥ 1500 mg/day or the maximum tolerated dose ;
  • A stable dose of metformin (≥ 1500 mg/day or the maximum tolerated dose ) in combination with SGLT2 inhibitors;
  • A stable dose of metformin (≥1500 mg/day or a maximum tolerated dose < 1500 but ≥ 1000 mg/day) in combination with a stable daily dose of sulfonylureas.
  • HbA1c ≥ 7.5% and ≤ 11% at screening (central laboratory).
  • BG < 15 mmol/L at screening (central laboratory).

Exclusion criteria

  • Type 1 diabetes mellitus or special type of diabetes mellitus.
  • Diabetic ketoacidosis, diabetic lactic acidosis or hyperosmolar state within 6 months before screening, or diabetic ketosis at screening/before randomization.
  • Severe chronic complications of diabetes (such as proliferative retinopathy or maculopathy, diabetic painful neuropathy, intermittent claudication, or diabetic foot) at screening or before randomization.
  • History of acute or chronic pancreatitis and pancreatic injury before screening.
  • History or relevant family history of medullary thyroid cancer, multiple endocrine neoplasia (MEN) 2A or 2B before screening.
  • Any laboratory test indicator meeting the following criteria at screening or before randomization:
  • Calcitonin level ≥ 50 ng/L (pg/mL) at screening.
  • ALT ≥ 3.0 × upper limit of normal (ULN) or AST ≥ 3.0 × ULN or total bilirubin ≥ 2.0 × ULN.
  • Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m2, calculated using CKD-EPI equation (see Appendix 3).
  • Fasting triglyceride (TG) ≥ 5.7 mmol/L or 500 mg/dL.
  • Blood amylase or lipase > 1.5 × ULN.
  • Hemoglobin ≤ 100 g/L for women and ≤ 110 g/L for men.

Treatment and study plan

GZR18

Drug

Administered SC

semaglutide

Drug

Administered SC

Primary outcomes

  1. Change from Baseline in Hemoglobin A1c (HbA1c)(%)

    Time frame: Baseline, Week 44

Secondary outcomes

  1. Change from baseline in mean 7-point self-measured blood glucose (SMBG)

    Time frame: week 44

  2. Proportion of subjects with salvage therapy.

    Time frame: week 44

  3. Change from baseline in weight (kg)

    Time frame: week 44

  4. Percent change in weight from baseline (%)

    Time frame: week 44

  5. Proportion of subjects with ≥ 5% and 10% decrease in weight from baseline.

    Time frame: week 44

  6. Treatment emergent adverse events (TEAEs)

    Time frame: week 44

Sponsors and collaborators

Lead sponsor

Gan & Lee Pharmaceuticals.

Industry

Registry information

Official study title

A Multicenter, Randomized, Active-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of GZR18 Injection in Chinese Subjects With Type 2 Diabetes Mellitus and Poor Blood Glucose Control by Metformin Monotherapy or in Combination With Sodium-dependent Glucose Transporter 2 (SGLT2) Inhibitors or Sulfonylureas

Acronym: Optimum 2

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 16, 2025
Registry last updated
Nov 25, 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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