A GLP-1 receptor agonist

GLP-1 receptor agonists, combined with nanoparticle delivery and synergistic agents, provide an effective treatment for NAFLD and NASH by reducing hepatic fat, improving liver function, and preventing fibrosis with minimal side effects.

WO2026125953A1PCT designated stage Publication Date: 2026-06-18MAHRAT REEM

Patent Information

Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
MAHRAT REEM
Filing Date
2025-10-10
Publication Date
2026-06-18

AI Technical Summary

Technical Problem

Current treatment options for non-alcoholic fatty liver disease (NAFLD) and its advanced form, non-alcoholic steatohepatitis (NASH), are limited, and there is an urgent need for effective therapeutic interventions that can reduce hepatic fat content, improve liver function, and prevent fibrosis while minimizing side effects.

Method used

The use of GLP-1 receptor agonists, such as liraglutide, semaglutide, exenatide, dulaglutide, or modified GLP-1 analogs, in combination with nanoparticle delivery systems for targeted liver delivery, along with synergistic agents like SGLT-2 inhibitors, PPAR agonists, FXR agonists, and statins, to enhance efficacy and reduce side effects.

🎯Benefits of technology

The GLP-1 receptor agonists effectively reduce hepatic fat content, improve insulin sensitivity, decrease liver inflammation, and prevent fibrosis, with reduced systemic side effects through tissue-specific delivery mechanisms.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present disclosure relates to a GLP-1 receptor agonists to treat non-alcoholic fatty liver disease (NAFLD) and its advanced form, non-alcoholic steatohepatitis (NASH). The present disclosure also relates to the pharmaceutical composition comprising GLP-1 receptor agonists alone or in combination with other therapeutic agents. Moreover, the present disclosure relates to the kit comprising the GLP-1 receptor agonists and delivery system.
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