Effectiveness and Safety of iGlarLixi (Insulin Glargine 100 U/mL Plus Lixisenatide) in Type 2 Diabetes According to the Timing of Daily Administration: Data from the REALI Pooled Analysis.

Fixed-ratio combination Insulin glargine Lixisenatide Time of administration Type 2 diabetes

Journal

Diabetes therapy : research, treatment and education of diabetes and related disorders
ISSN: 1869-6953
Titre abrégé: Diabetes Ther
Pays: United States
ID NLM: 101539025

Informations de publication

Date de publication:
Apr 2023
Historique:
received: 16 12 2022
accepted: 23 01 2023
medline: 15 2 2023
pubmed: 15 2 2023
entrez: 14 2 2023
Statut: ppublish

Résumé

iGlarLixi (insulin glargine 100 U/mL plus lixisenatide) has demonstrated glycaemic efficacy and safety in adults with inadequately controlled type 2 diabetes mellitus (T2DM). Per the European Medicines Agency's product label, iGlarLixi should be injected once a day within 1 h prior to a meal, preferably the same meal every day when the most convenient meal has been chosen. It is however unknown whether iGlarLixi administration timing affects glycaemic control and safety, as clinical trial evidence is mainly based on pre-breakfast iGlarLixi administration. Therefore, we assessed the effectiveness and safety of iGlarLixi in clinical practice, according to its administration timing. Data were pooled from two prospective observational studies including 1303 European participants with T2DM inadequately controlled on oral antidiabetic drugs with or without basal insulin who initiated iGlarLixi therapy for 24 weeks. Participants were classified into four subgroups based on daily timing of iGlarLixi injection: pre-breakfast (N = 436), pre-lunch (N = 262), pre-dinner (N = 399), and those who switched iGlarLixi injection time during the study (N = 206). No meaningful differences in baseline characteristics were observed between the study groups. Least-squares mean reductions in haemoglobin A1c (HbA1c) from baseline to week 24 were substantial in all groups, with the numerically largest decrease observed in the pre-breakfast group (1.57%) compared with the pre-lunch (1.27%), pre-dinner (1.42%), or changed injection time (1.33%) groups. Pre-breakfast iGlarLixi injection also resulted in a numerically greater proportion of participants achieving HbA1c < 7.0% at week 24 (33.7% versus 19.0% for pre-lunch, 25.6% pre-dinner, and 23.2% changed injection time). iGlarLixi was well tolerated across all groups, with low rates of gastrointestinal disorders and hypoglycaemia. Mean body weight decreased similarly in all groups (by 1.3-2.3 kg). iGlarLixi was effective and safe regardless of its daily administration time. However, pre-breakfast iGlarLixi injection resulted in a more effective glycaemic control.

Identifiants

pubmed: 36787044
doi: 10.1007/s13300-023-01375-8
pii: 10.1007/s13300-023-01375-8
pmc: PMC10064361
doi:

Types de publication

Journal Article

Langues

eng

Pagination

639-652

Informations de copyright

© 2023. The Author(s).

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Auteurs

Martin Haluzík (M)

Institute for Clinical and Experimental Medicine and Charles University, Prague, Czech Republic.

Jochen Seufert (J)

Division of Endocrinology and Diabetology, Department of Medicine II, Medical Centre-Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Cristian Guja (C)

Department of Diabetes, Nutrition and Metabolic Diseases, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Mireille Bonnemaire (M)

General Medicines, Sanofi, Paris, France. mireille.bonnemaire@sanofi.com.

Gregory Bigot (G)

IVIDATA Group, Paris, France.

Mathilde Tournay (M)

International Drug Development Institute (IDDI), Louvain-la-Neuve, Belgium.

János Tibor Kis (JT)

Department of Internal Medicine Centrum, Szent János Hospital, Budapest, Hungary.

Nick Freemantle (N)

Institute of Clinical Trials and Methodology, University College London, London, UK.

Classifications MeSH