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Background: Inadequate dose titration and poor adherence to basal insulin can lead to suboptimal glycemic control in persons with type 2 diabetes (T2D). Once-weekly insulin icodec (icodec) is a basal insulin analogue that is in development and is aimed at reducing treatment burden.
Objective: To compare the effectiveness and safety of icodec titrated with a dosing guide app (icodec with app) versus once-daily basal insulin analogues (OD analogues) dosed per standard practice.
Design: 52-week, randomized, open-label, parallel-group, phase 3a trial with real-world elements. (ClinicalTrials.gov: NCT04760626).
Setting: 176 sites in 7 countries.
Participants: 1085 insulin-naive adults with T2D.
Intervention: Icodec with app or OD analogue (insulin degludec, insulin glargine U100, or insulin glargine U300).
Measurements: The primary outcome was change in glycated hemoglobin (HbA) level from baseline to week 52. Secondary outcomes included patient-reported outcomes (Treatment Related Impact Measure for Diabetes [TRIM-D] compliance domain score and change in Diabetes Treatment Satisfaction Questionnaire [DTSQ] total treatment satisfaction score).
Results: The estimated mean change in HbA level from baseline to week 52 was greater with icodec with app than with OD analogues, with noninferiority ( < 0.001) and superiority ( = 0.009) confirmed in prespecified hierarchical testing (estimated treatment difference [ETD], -0.38 percentage points [95% CI, -0.66 to -0.09 percentage points]). At week 52, patient-reported outcomes were more favorable with icodec with app than with OD analogues (ETDs, 3.04 [CI, 1.28 to 4.81] for TRIM-D and 0.78 [CI, 0.10 to 1.47] for DTSQ). Rates of clinically significant or severe hypoglycemia were low and similar with both treatments.
Limitation: Inability to differentiate the effects of icodec and the dosing guide app.
Conclusion: Compared with OD analogues, icodec with app showed superior HbA reduction and improved treatment satisfaction and compliance with similarly low hypoglycemia rates.
Primary Funding Source: Novo Nordisk A/S.
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http://dx.doi.org/10.7326/M23-1288 | DOI Listing |
Diabetes Obes Metab
October 2025
Department of Internal Medicine/Endocrinology, and Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Aims: In ONWARDS 5 (NCT04760626), a 52-week, Phase 3a trial in insulin-naive type 2 diabetes, 542/1085 participants were randomized to once-weekly insulin icodec with a dosing guide app to assist titration (icodec with app). This post hoc analysis of the icodec with app group assessed titration behaviours and associations between app-based dose guidance adherence and outcomes.
Materials And Methods: App-based dose guidance and manual overrides were assessed.
Diabetes Ther
February 2025
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Introduction: ONWARDS 5 evaluated the effectiveness and safety of insulin icodec (icodec) titrated with a dosing guide app (icodec with app) versus once-daily insulin analogs in insulin-naive adults with type 2 diabetes. The insulin glargine U300 (glargine U300) stratum was too small to enable a robust post hoc efficacy comparison. Augmentation methodology was applied to increase the glargine U300 group size using real-world data (RWD), to facilitate efficacy comparisons of icodec with app versus glargine U300, and to demonstrate the potential of the augmentation methodology to strengthen underpowered treatment comparisons (AUGMENT study).
View Article and Find Full Text PDFDiabetes Res Clin Pract
November 2024
LMC Diabetes & Endocrinology, Concord, ON, Canada.
Ann Intern Med
January 2024
Aristotle University Thessaloniki, Thessaloniki, Greece (A.L., T.K., A.T.).
Bajaj HS, Aberle J, Davies M, et al. Ann Intern Med. 2023;176:1476-1485.
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