Achievement of glycaemic targets with weight loss and without hypoglycaemia in type 2 diabetes with the once-weekly glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist tirzepatide: A post hoc analysis of the SURPASS-1 to -5 studies.


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
04 2023
Historique:
revised: 30 11 2022
received: 03 10 2022
accepted: 08 12 2022
pubmed: 15 12 2022
medline: 8 3 2023
entrez: 14 12 2022
Statut: ppublish

Résumé

To assess composite endpoints combining glycaemic control (HbA1c < 7.0%, ≤ 6.5% or < 5.7%) with weight loss (≥ 5%, ≥ 10% or ≥ 15%) and without hypoglycaemia with tirzepatide in type 2 diabetes (T2D). Data from the phase 3 SURPASS programme were evaluated post hoc by trial. Participants with T2D were randomized to tirzepatide (5, 10 and 15 mg), placebo (SURPASS-1,5), semaglutide 1 mg (SURPASS-2) or titrated basal insulin (SURPASS-3,4). The proportions of participants achieving the composite endpoints were compared between tirzepatide and the respective comparator groups at week 40/52. The proportions of participants achieving an HbA1c value of less than 7.0% with 5% or more weight loss and without hypoglycaemia ranged from 43% to 82% with tirzepatide across the SURPASS-1 to -5 trials versus 4%-5% with placebo, 51% with semaglutide 1 mg and 5% with basal insulin (P < .001 vs. all comparators). The proportions of participants achieving an HbA1c value of less than 7.0% with 10% or more, or 15% or more weight loss and without hypoglycaemia were significantly higher with all tirzepatide doses versus comparators across trials (P < .001 or P < .05). Similar results were observed for all other combinations of endpoints with an HbA1c value of 6.5% or less, or less than 5.7%, with more tirzepatide-treated participants achieving these endpoints versus those in the comparator groups, including semaglutide. Across the SURPASS-1 to -5 clinical trials, more tirzepatide-treated participants with T2D achieved clinically meaningful composite endpoints, which included reaching glycaemic targets with various degrees of weight loss and without hypoglycaemia, than those in the comparator groups.

Identifiants

pubmed: 36514843
doi: 10.1111/dom.14943
doi:

Substances chimiques

Hypoglycemic Agents 0
tirzepatide OYN3CCI6QE
Glucagon-Like Peptide-1 Receptor 0
Glycated Hemoglobin 0
Gastric Inhibitory Polypeptide 59392-49-3
Insulins 0
Glucose IY9XDZ35W2

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

965-974

Informations de copyright

© 2022 Eli Lilly and Company. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

Références

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Auteurs

Ildiko Lingvay (I)

Department of Internal Medicine/Endocrinology and Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.

Alice Yy Cheng (AY)

Division of Endocrinology and Metabolism, Department of Medicine, Trillium Health Partners and Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.

Joshua A Levine (JA)

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana.

Elisa Gomez-Valderas (E)

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana.

Sheryl E Allen (SE)

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana.

Kari Ranta (K)

Eli Lilly and Company, Helsinki, Finland.

Amelia Torcello-Gómez (A)

Eli Lilly and Company, Cork, Ireland.

Vivian T Thieu (VT)

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana.

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