[8] Merck steps into NASH space with early data for its GLP-1/glucagon receptor co-agonist. Retrieved June 14, 2023, from https://endpts.com/merck-steps-into-liver-disease-space-with-early-data-for-its-glp-1-glucagon-receptor-co-agonist/ [9] Can Novo Nordisk's blockbuster weight loss ...
[2] Wharton, Sean et al. “Daily Oral GLP-1 Receptor Agonist Orforglipron for Adults with Obesity.” The New England journal of medicine vol. 389,10 (2023): 877-888. doi:10.1056/NEJMoa2302392 [3] Wilding, John P H et al. “Onc...
[8] Merck steps into NASH space with early data for its GLP-1/glucagon receptor co-agonist. Retrieved June 14, 2023, from https://endpts.com/merck-steps-into-liver-disease-space-with-early-data-for-its-glp-1-glucagon-receptor-co-agonist/ [9] Can Novo Nordisk's blockbuster weight loss ...
GLP-1 agonist medications work bymimickingthis hormone. In medication terms, anagonistis amanufacturedsubstance that attaches to a cell receptor and causes the same action as the naturally occurring substance. In other words, GLP-1 medications bind to GLP receptors to trigger the effects (or roles...
[10] Frias, J. P. Tirzepatide: a glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) dual agonist in development for the treatment of type 2 diabetes. Expert Rev Endocrinol Metab. 2020, 15, 379-394. ...
GLP⁃１是一种由 30个氨基酸组成的肠促胰岛素激素，餐后由我们人体的回肠远端、结肠近端和迷走神经的L...
[3]LY3437943, a novel triple GIP, GLP-1, and glucagon receptor agonist in people with type 2 diabetes: a phase 1b, multicentre, double-blind, placebo-controlled, randomised,multiple-ascending dose trial. [4]行行查.
（图片来源：《Triple–Hormone-Receptor Agonist Retatrutide for Obesity— A Phase 2 Trial》）在主要临床终点上，24周时，体重百分比方面，1 mg Retatrutide组为-7.2%，4 mg组为-12.9%，8mg组为-17.3%，而12 mg的组达到了-17.5%，安慰剂组为-1.6%。此外，次要临床终点48周的体重变化上，12mg组的...
8 Fan, H. et al. The non-peptide GLP-1 receptor agonist WB4-24 blocks inflammatory nociception by stimulating beta-endorphin release from spinal microglia.Br J Pharmacol172, 64-79, doi:10.1111/bph.12895 (2015). 转载须知 【非原创文章】本文著作权归文章作者所有,欢迎个人转发分享,未经作者的允许...
优点是突破产能瓶颈，更适合大规模连续生产，通过优化生物发酵过程和利用微生物高效的生物合成能力，能够进一步降低生产成本。资料来源：Drug Des Devel Ther. Lijing Wang，《Designing a Dual GLP-1R/GIPR Agonist from Tirzepatide: Comparing Residues Between Tirzepatide, GLP-1, and GIP》，X技术，国知局，...