Peptain
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Liraglutide

Also sold as Saxenda, Victoza.

Half-life
13 h
Steady state
~3 d
Class
GLP-1
Category
GLP-1

Published population averages. Steady state is the usual five half-life rule of thumb, not a measurement. See peptide half-life, explained.

Overview

Liraglutide is a GLP-1 receptor agonist with 97% structural homology to native GLP-1. Approved for T2DM (Victoza, 1.8 mg daily) and obesity (Saxenda, 3.0 mg daily). It was one of the first GLP-1 agents to demonstrate cardiovascular benefit in the LEADER trial.

How it works

Binds GLP-1 receptors similarly to semaglutide but with a shorter C-16 fatty acid side chain (palmitoyl), resulting in shorter duration. Enhances glucose-dependent insulin secretion, suppresses glucagon, delays gastric emptying, and reduces appetite. Self-associates into heptamers at the injection site, creating a slow-release depot.

Half-life and peak

Terminal half-life is approximately 13 hours, requiring daily dosing. Peak plasma concentration is reached 8–12 hours post-injection. Steady state achieved within 3 days.

What it is studied for

T2DM glycemic control, chronic weight management, cardiovascular outcomes (LEADER trial), pediatric obesity.

Research status

FDA-approved for T2DM (Victoza, 2010) and weight management (Saxenda, 2014). LEADER trial showed 13% cardiovascular benefit. Well-established safety profile.

Sources

Educational reference only. This page describes what is published about a compound; it is not medical advice, not a recommendation to take anything, and not a dosing guide. Several compounds in this catalog are investigational and are not approved medicines. Talk to a doctor.

Guides that cover it