Drug intelligence / Profile preview

insulin + metformin + polyethylene glycol loxenatide

Development stage
Preclinical
Lead developer
Hansoh Pharmaceutical Group
Modality
Small Molecules, Recombinant Proteins and Enzymes, Peptides, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Oral, Subcutaneous
01

Overview

This is a fixed-dose combination therapy consisting of three active pharmaceutical ingredients used in the management of type 2 diabetes mellitus: - **Insulin** is a peptide hormone that regulates blood glucose by promoting cellular uptake of glucose and inhibiting hepatic glucose production. - **Metformin** is a biguanide oral antihyperglycemic agent that decreases hepatic gluconeogenesis, increases peripheral insulin sensitivity, and reduces intestinal absorption of glucose[3][6][9]. - **Polyethylene glycol loxenatide (PEG-Loxe)** is a long-acting glucagon-like peptide 1 receptor agonist (GLP-1RA), derived from exendin-4 and modified with polyethylene glycol to extend its half-life. It stimulates insulin secretion in a glucose-dependent manner, suppresses glucagon secretion, slows gastric emptying, and promotes weight loss[7][10]. The combination targets multiple pathophysiological mechanisms in type 2 diabetes—insulin deficiency/resistance (insulin), impaired hepatic regulation (metformin), and incretin pathway dysfunction (PEG-loxenatide). PEG-loxenatide has demonstrated efficacy both as monotherapy and in combination with metformin for glycemic control and weight reduction[7][10]. This triple therapy may be considered for patients inadequately controlled on dual or monotherapy.

02

Targets

ND1 (Mitochondrial electron transport chain complex I)INSR (Insulin receptor)GLP1R (GLP-1R)

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