Triagonist for GLP-1r, GIPR, and gcgr

By designing GLP-1R, GIPR and GCGR triple agonist compounds of specific polypeptide sequences, the limitations of existing drugs in weight loss and glucose reduction effects are solved, and better therapeutic effects of metabolic disorders are achieved.

WO2025162423A1 Publication Date: 2025-08-07HANG ZHOU SCIWIND BIOSCIENCES CO LTD +1
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Patent Information

Application Number
PCT/CN2025/075383
Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Priority Date
2024-02-02
Filing Date
2025-01-27
Publication Date
2025-08-07

AI Technical Summary

Technical Problem

The existing GLP-1R/GIPR/GCGR dual-target drugs have limitations in weight loss and glucose reduction effects, and it is difficult to design multiple active peptides, which is difficult to meet clinical needs.

Method used

A GLP-1R, GIPR and GCGR triple agonist compound with a completely new polypeptide sequence is developed, synthesized by chemical or biological methods, containing specific amino acid sequences and connecting fatty acid side chains to Lys residues, improving activity and stability.

Benefits of technology

It has achieved better blood sugar control and weight loss effects, and showed drug performance that is better than the existing three agonists, which is suitable for the treatment of metabolic disorders such as diabetes and obesity.

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Abstract

A triagonist for GLP-1R, GIPR, and GCGR, which can be used for preventing and / or treating metabolic disorders.
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