Drug intelligence / Profile preview

saroglitazar magnesium

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

Overview

Saroglitazar magnesium is a dual peroxisome proliferator-activated receptor (PPAR) agonist. It is the magnesium salt (2:1) of saroglitazar, which is its parent compound. Through dual activation of PPAR-α and PPAR-γ, it aims to regulate both lipid and glucose homeostasis. The PPAR-α activation leads to increased hepatic oxidation of fatty acids, reduced synthesis and secretion of triglycerides, increased lipolysis, activation of lipoprotein lipase (LPL), reduced production of Apo C-III, reduced plasma LDL-C, and increased synthesis of apolipoproteins A-I and A-II, and HDL-C. In India, saroglitazar (as Lipaglyn™) is approved for diabetic dyslipidemia and hypertriglyceridemia with type 2 diabetes mellitus not controlled by statin therapy. It is also being investigated for other conditions including primary biliary cholangitis (PBC) and nonalcoholic steatohepatitis (NASH).

Brand names
Lipaglyn
Other names
Saroglitazar
02

Targets

PPARG (Peroxisome proliferator-activated receptor gamma)PPARA (Peroxisome proliferator-activated receptor alpha)

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