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IGlarLixi: A New Once-Daily Fixed-Ratio Combination of Basal Insulin Glargine and Lixisenatide for the Management of Type 2 Diabetes

Overview
Journal Diabetes Spectr
Specialty Endocrinology
Date 2018 May 19
PMID 29773934
Citations 13
Authors
Affiliations
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Abstract

Background: Patients with type 2 diabetes require treatment intensification to maintain glycemic control. Clinician reluctance, patient injection fears, hypoglycemia, weight gain, or other objections may lead to clinical inertia, whereby therapy is not intensified and patients live with uncontrolled hyperglycemia and increased risk for complications. Initiation of injectable therapy with a glucagon-like peptide (GLP)-1 receptor agonist and/or basal insulin is a recommended option for patients with type 2 diabetes inadequately controlled on one or more oral agents.

Purpose: This article reviews clinical evidence and provides information on dosing and administration of iGlarLixi, a titratable fixed-ratio combination of insulin glargine and the GLP-1 receptor agonist lixisenatide that effectively lowers both fasting and postprandial glucose levels.

Findings: In phase 3 trials, iGlarLixi provided greater A1C reduction than insulin glargine or lixisenatide alone, without increased hypoglycemia risk compared with insulin glargine. iGlarLixi did not lead to weight gain versus insulin glargine and was associated with a lower frequency of gastrointestinal adverse effects than lixisenatide. iGlarLixi was recently approved by the U.S. Food and Drug Administration to improve glycemic control in adults with type 2 diabetes inadequately controlled on basal insulin (<60 units daily) or lixisenatide. iGlarLixi is administered by subcutaneous injection once daily, and the dose is titrated based on each patient's insulin needs using a simple titration algorithm.

Conclusion: iGlarLixi offers an effective and well-tolerated treatment option for patients with type 2 diabetes requiring additional glycemic control, with comparable or improved safety outcomes than its separate components. Because of its simple regimen and low rate of adverse effects, iGlarLixi may improve adherence and, consequently, therapeutic outcomes.

Citing Articles

Pharmacokinetics and Safety of iGlarLixi in Healthy Chinese Participants: Results of a Phase 1 Randomized Study.

Xie P, He X, Gao X, Shuai M, Schmider W, Jiang A Diabetes Ther. 2023; 14(8):1387-1397.

PMID: 37329393 PMC: 10299984. DOI: 10.1007/s13300-023-01434-0.


Clinical Benefits of Treating Patients with Type 2 Diabetes Mellitus with iGlarLixi: A Patient-Level Simulation Study.

Chauhan A, Samnaliev M, Ken-Opurum J, Srinivas S, Mehta A, Dex T Diabetes Ther. 2023; 14(8):1331-1344.

PMID: 37289358 PMC: 10299979. DOI: 10.1007/s13300-023-01419-z.


Expert Opinion on Diabetes Management Challenges and Role of Basal Insulin/GLP-1 RA Fixed-Ratio Combination in People with Type 2 Diabetes from Indonesia.

Suastika K, Eliana F, Kshanti I, Mardianto M, Mudjarnako S, Natalia N Diabetes Metab Syndr Obes. 2022; 15:2977-2990.

PMID: 36193540 PMC: 9526452. DOI: 10.2147/DMSO.S367153.


Treatment persistence and adherence in people with type 2 diabetes switching to iGlarLixi vs free-dose combinations of basal insulin and glucagon-like peptide 1 receptor agonist.

Edelman S, Cassarino D, Kayne D, Dex T, Li X, Pasquel F J Manag Care Spec Pharm. 2022; 28(9):958-968.

PMID: 36001104 PMC: 10373043. DOI: 10.18553/jmcp.2022.28.9.958.


Transitioning from basal-bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes.

Mehta R, Billings L, Liebl A, Vilsboll T Diabet Med. 2022; 39(9):e14901.

PMID: 35708737 PMC: 9542161. DOI: 10.1111/dme.14901.


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