Lixisenatide: first global approval.
Drugs · 2013
Last updated 2026-05-28Lixisenatide is a once-daily injectable drug for type 2 diabetes that mimics a natural hormone to help control blood sugar. It has been approved in the EU, Iceland, Liechtenstein, Norway, and Mexico, and is under review in several other countries including the USA.
AI summary of the abstract below.
| Journal | Drugs, 2013 |
|---|---|
| Citations | 26 |
| Relative citation ratio | 0.85 |
| NIH percentile | 45 |
| Molecules | lixisenatide |
| Conditions studied | Type 2 Diabetes |
Abstract
The selective once-daily prandial glucagon-like peptide-1 (GLP-1) receptor agonist lixisenatide (Lyxumia(®)) is under development with Sanofi for the treatment of type 2 diabetes mellitus. Lixisenatide belongs to a class of GLP-1 compounds designed to mimic the endogenous hormone GLP-1. Native GLP-1 stimulates insulin secretion in a glucose-dependent manner, as well as suppressing glucagon production and slowing gastric emptying. A once-daily subcutaneous formulation of lixisenatide has been approved in the EU, Iceland, Liechtenstein, Norway and Mexico for the treatment of type 2 diabetes, and is under regulatory review in the USA, Switzerland, Brazil, Canada, Ukraine, South Africa, Japan and Australia. This article summarizes the milestones in the development of lixisenatide, leading to this first approval for use in adults with type 2 diabetes.
Verbatim abstract via PubMed 23558600 ↗
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- Contrasting Effects of Lixisenatide and Liraglutide on Postprandial Glycemic Control, Gastric Emptying, and Safety Parameters in Patients With Type 2 Diabetes on Optimized Insulin Glargine With or Without Metformin: A Randomized, Open-Label Trial.
- Benefits of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide, Versus Insulin Glargine and Lixisenatide Monocomponents in Type 2 Diabetes Inadequately Controlled on Oral Agents: The LixiLan-O Randomized Trial.