Literature DB >> 32072742

Efficacy and safety of insulin glargine/lixisenatide fixed-ratio combination (iGlarLixi) in Japanese patients with type 2 diabetes mellitus inadequately controlled on basal insulin and oral antidiabetic drugs: The LixiLan JP-L randomized clinical trial.

Hideaki Kaneto1, Akane Takami2, Robert Spranger3, Atsushi Amano2, Daisuke Watanabe2, Elisabeth Niemoeller3.   

Abstract

AIMS: To assess efficacy and safety of fixed-ratio (1:1) combination insulin glargine and lixisenatide (iGlarLixi) compared to insulin glargine U100 (iGlar), with metformin, in Japanese patients with type 2 diabetes mellitus (T2DM) inadequately controlled on basal insulin and oral antidiabetic drugs (OADs).
MATERIALS AND METHODS: This 26-week, randomized, open-label study compared iGlarLixi to iGlar, both with metformin in adult Japanese patients with T2DM and hemoglobin (Hb) A1c ≥7.5% to ≤9.5%, treated with basal insulin and 1 or 2 OADs. Five hundred and twelve patients were randomized after a 12-week run-in, when iGlar was introduced and/or further titrated and OADs other than metformin were stopped. The primary endpoint was change in HbA1c from baseline to week 26.
RESULTS: iGlarLixi (n = 255) demonstrated significantly greater reductions in HbA1c (-1.27%) than iGlar (n = 257, -0.53%) (LS mean difference: -0.74%, P < .0001) at week 26, confirming the superiority of iGlarLixi. Significantly, more iGlarLixi patients reached target HbA1c <7% at week 26 (51.8% vs 16.0% for iGlar). iGlarLixi patients lost weight in contrast to iGlar patients (-0.51 kg vs +0.55 kg). Documented symptomatic hypoglycemia (plasma glucose ≤ 3.9 mmol/L) was observed in 18.8% of iGlarLixi patients vs 16.7% of iGlar patients. iGlarLixi patients had more gastrointestinal-related adverse events than iGlar patients (33.3% vs 8.6%), primarily nausea (16.9% vs 0.8%). However, the treatment was generally well-tolerated.
CONCLUSIONS: A once-daily injection of iGlarLixi with metformin is an effective, well-tolerated, and simple therapeutic intervention providing significant improvement in glycemic control in Japanese patients with T2DM inadequately controlled on basal insulin and up to two OADs. Clinical Trial Number: NCT02752412.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  GLP-1 analogue; basal insulin; glycemic control; metformin; phase 3 study; type 2 diabetes

Mesh:

Substances:

Year:  2020        PMID: 32072742     DOI: 10.1111/dom.14005

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  3 in total

1.  Efficacy and safety of iGlarLixi versus IDegAsp: Results of a systematic literature review and indirect treatment comparison.

Authors:  Philip D Home; Roopa Mehta; Khadija A S Hafidh; Olesya Y Gurova; Agustina Alvarez; Paul Serafini; Mir-Masoud Pourrahmat
Journal:  Diabetes Obes Metab       Date:  2021-08-31       Impact factor: 6.408

2.  iGlarLixi reduces residual hyperglycemia in Japanese patients with type 2 diabetes uncontrolled on basal insulin: A post-hoc analysis of the LixiLan JP-L trial.

Authors:  Daisuke Yabe; Katsumi Iizuka; Mike Baxter; Daisuke Watanabe; Hideaki Kaneto
Journal:  J Diabetes Investig       Date:  2021-06-19       Impact factor: 4.232

3.  Benefit of insulin glargine/lixisenatide for reducing residual hyperglycaemia in Japan: Post hoc analysis of the LixiLan JP-O2 trial.

Authors:  Katsumi Iizuka; Mike Baxter; Daisuke Watanabe; Daisuke Yabe
Journal:  Diabetes Obes Metab       Date:  2021-09-23       Impact factor: 6.408

  3 in total

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