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Friday, March 11 2022 - 03:18
AsiaNet
Gan & Lee Pharmaceuticals Begins First-In-Human Trial in U.S. for Investigational Drug, GZR18
BEIJING and BRIDGEWATER, N.J., Mar 10, 2022, /PRNewswire-AsiaNet/--

Gan & Lee Pharmaceuticals Co., Ltd. (hereinafter referred to as Gan & Lee, 
stock code: 603087.SH), is pleased to announce the first subject has been dosed 
in our Phase I, double-blinded, randomized, placebo-controlled, sequential, 
single, ascending dose clinical study in the U.S. for the company’s 
investigational drug, GZR18. GZR18 is a glucagon-like peptide-1 receptor 
agonist (GLP-1RA) with potential to treat patients with type 2 diabetes. 
Currently, type 2 diabetes mellitus accounts for approximately 90% of all 
diabetes cases while a 46% increase in the number of people with diabetes is 
expected by 2045, globally[1]. Glucagon-like peptide-1 (GLP-1) is an incretin 
hormone responsible for many glucoregulatory effects such as the stimulation of 
insulin secretion and the inhibition of glucagon when blood glucose is high[2]. 
Many of these glucoregulatory effects are often impaired in patients with type 
2 diabetes[3]. 

The primary objective of this Phase 1 study is to investigate the safety and 
tolerability of GZR18 in healthy volunteers. In addition, the secondary 
objective is to determine the pharmacokinetic (PK) parameters of GZR18. “The 
start of this Phase 1 clinical trial of GZR18 at a U.S. site, is a significant 
milestone for our global clinical development program. This trial demonstrates 
Gan & Lee’s long-term commitment to strengthening our pipeline in diabetes and 
other therapeutic areas to benefit the patient and medical community” said Dr. 
Mike Hu, the Chief Executive Officer (CEO) & President of Gan & Lee 
Pharmaceuticals USA Corporation.  

About Gan & Lee
Gan & Lee Pharmaceuticals has developed the first Chinese domestic biosynthetic 
human insulin. Currently, we have five recombinant insulin analogs 
commercialized in China including 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). We have two approved medical 
devices in China, namely reusable insulin injection pen (GanleePen™), and 
disposable pen needle (GanleeFine®).
In the future, Gan & Lee strives to achieve a comprehensive coverage in the 
field of diabetes diagnosis and treatment. Moving forward to advance our goal 
of becoming a world-class pharmaceutical company, we will also take an active 
part in developing new chemical entities, and work on the treatment of 
cardiovascular diseases, metabolic diseases, cancer, and other therapeutics. 
For more information, please contact us at investorrelations@ganlee.us.

References
[1].	International Diabetes Federation. IDF Diabetes Atlas, 10th edn. Brussels, 
Belgium: 2021. Available at: https://www.diabetesatlas.org 
[2].	Nauck MA, Quast DR, Wefers J, Meier JJ. GLP-1 receptor agonists in the 
treatment of type 2 diabetes - state-of-the-art. Mol Metab. 2021 Apr; 
46:101102. doi: 10.1016/j.molmet.2020.101102. Epub 2020 Oct 14. PMID: 33068776; 
PMCID: PMC8085572. Available at: https://www.ncbi.nlm.nih.gov/books/NBK551568/
[3].	Brunton SA, Wysham CH. GLP-1 receptor agonists in the treatment of type 2 
diabetes: role and clinical experience to date. Postgrad Med. 2020 
Nov;132(sup2):3-14. doi: 10.1080/00325481.2020.1798099. Epub 2020 Sep 8. PMID: 
32815454.

Media Contacts: Gina Antonucci, #: 888-288-5395, investorrelations@ganlee.us 

Source: Gan & Lee Pharmaceuticals Co., Ltd.
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