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Home / Company News / Gan & Lee Pharmaceuticals Announced First Participant Dosed in a phase 3b Clinical Stufy (SUPER-8) of Once-weekly Basal Insulin GZR4 Injection in Chinese Adults with Type 2 Diabetes Mellitus
Gan & Lee Pharmaceuticals Announced First Participant Dosed in a phase 3b Clinical Stufy (SUPER-8) of Once-weekly Basal Insulin GZR4 Injection in Chinese Adults with Type 2 Diabetes Mellitus
Date:2025-10-17

Beijing, China, October 17, 2025 — Gan & Lee Pharmaceuticals (hereinafter referred to as "Gan & Lee" stock code: 603087.SH) announced that the first participants has been dosed in a large phase 3b clinical study (SUPER-8), evaluating its once-weekly basal insulin GZR4 injection in Chinese adults with type 2 diabetes mellitus (T2DM) who were previously treated with basal insulin therapy. SUPER-8 is the fourth large-scale phase 3 clinical study conducted for GZR4 injection.


This phase 3b clinical study (clinicaltrials.gov registration number: NCT07165223) designed to compare the efficacy, safety, and patient-reported outcomes of GZR4 injection and Insulin Icodec with or without non-insulin antidiabetic agents in participants with T2DM treated with basal insulin. Professor Ming Liu from Tianjin Medical University General Hospital is the leading principal investigator of SUPER-8. The study plans to enroll 300 participants who will be randomized to receive either GZR4 injection or insulin Icodec. The primary endpoint is the change in glycated hemoglobin (HbA1c) from baseline at week 26.


GZR4 injection has previously conducted three phase 3 clinical trials (SUPER-1 to SUPER-3) in Chinese adults with T2DM, comparing GZR4 injection with once-daily basal insulin regimens in terms of glycemic efficacy and safety. This phase 3b head-to-head SUPER-8 study will further validate the efficacy and safety profile of GZR4 injection.


About GZR4

Gan & Lee Pharmaceuticals' independently developed GZR4  injection is an ultra-long-acting weekly insulin preparation that is expected to provide more stable glucose-lowering effects and reduced intra- or inter-day blood glucose variability. GZR4 is anticipated to help patients with diabetes overcome injection barriers, enable earlier initiation of insulin therapy, optimize long-term diabetes management, and enhance patients' quality of life via once-weekly subcutaneous injection. Early clinical findings indicate that GZR4 demonstrates comparable reduction in HbA1c to insulin degludec in patients with inadequate glycemic control through oral antidiabetic medications. Currently, the global development of GZR4 has entered the Phase 3 clinical trial stage.

 

Forward-looking statements

Forward-looking statements are based on our expectations and assumptions as of the date of the statements. Actual results may differ materially from those expressed in these forward-looking statements due to a variety of factors, and we can give no assurance that such results will be achieved in the future. We undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise.


About Gan & Lee

Gan & Lee Pharmaceuticals developed the first Chinese domestic insulin analog. Currently, Gan & Lee has six core insulin products, including five insulin analog varieties: long-acting glargine injection (Basalin®), fast-acting lispro injection (Prandilin™), fast-acting aspart injection (Rapilin®), mixed protamine zinc lispro injection (25R) (Prandilin™25), aspart 30 injection (Rapilin®30), and one human insulin injection - mixed protamine human insulin injection (30R) (Similin®30). The company has two approved medical devices in China, namely reusable insulin injection pen (GanleePen), and disposable pen needle (GanleeFine®).

 

In China's 2024 National Insulin-Specific Centralized Procurement, Gan & Lee Pharmaceuticals ranked  first among all selected companies in terms of procurement demand for insulin analogs. The company is also making strides in international markets, with the disposable pen needle (GanleeFine®) approved by the US Food and Drug Administration (FDA) in 2020 and received GMP inspection approval from the European Medicines Agency (EMA) in 2024. These achievements significantly boost Gan & Lee’s competitiveness in both international and domestic markets.

 

In the future, Gan & Lee will strive for comprehensive coverage in diabetes treatment. Moving forward with its mission to become a world-class pharmaceutical company, Gan & Lee will also actively develop new chemical entities and biological drugs, focusing on treatments for metabolic diseases, cardiovascular diseases, and other therapeutic areas.

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