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Article Abstract

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/M23-1288DOI Listing

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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.

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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).

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Article Synopsis
  • The ONWARDS phase 3a trials compared once-weekly insulin icodec to once-daily basal insulin for managing type 2 diabetes, focusing on participant and physician experiences.
  • Patient-reported outcomes showed significantly greater treatment satisfaction with insulin icodec, particularly due to its less frequent injection schedule and ease of use.
  • Both participants and physicians expressed a strong preference for once-weekly injections over daily ones, highlighting the advantages of convenience and willingness to continue treatment.
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