Drug intelligence / Profile preview

chiglitazar

Development stage
Phase 3
Lead developer
Akeso
Modality
Small Molecules
Administration
Oral
01

Overview

Chiglitazar is a novel small molecule drug developed as a peroxisome proliferator-activated receptor (PPAR) pan-agonist. It simultaneously activates all three PPAR subtypes (α, γ, and δ), leading to improved insulin sensitivity and regulation of glucose and lipid metabolism. By targeting the core pathophysiology of type 2 diabetes—insulin resistance—chiglitazar modulates gene expression related to fatty acid oxidation, energy conversion, and lipid transport. It is the world’s first approved PPAR pan-agonist for type 2 diabetes mellitus (T2DM), offering a new mechanism distinct from existing antidiabetic agents. The drug was independently developed in China by Chipscreen Biosciences and is indicated for improving glycemic control in adults with T2DM as monotherapy or in combination with other agents such as metformin. Clinical studies have also explored its use in nonalcoholic steatohepatitis (NASH). Metabolism occurs primarily via hepatic CYP3A enzymes[1][2][4][6].

Brand names
双洛平Bilessglu
Other names
西格列他钠Chiglitazar Sodium Tablets
02

Targets

PPARD (Peroxisome proliferator–activated receptor delta)PPARA (Peroxisome proliferator-activated receptor alpha)PPARG (Peroxisome proliferator-activated receptor gamma)

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