# Automated basal insulin delivery versus multiple daily injections in type 1 diabetes: results from a randomized parallel controlled trial

**Authors:** Johan H. Jendle, Satish K. Garg, Charles Thivolet, Ruth S. Weinstock, Irl B. Hirsch, Mark Evans, Kurt J. Griffin, Athena Philis-Tsimikas, Benjamin J. Wheeler, Mark S. Kipnes, Anders L. Carlson, Bruce A. Buckingham, Anuj Bhargava, Bruce W. Bode, Margaret L. Lawson, Amy B. Criego, Janet B. McGill, John “Chip” H. Reed, Gnanagurudasan Prakasam, George Grunberger, Angela Girelli, María Asunción Martinez-Brocca, Mark P. Christiansen, Martin I. de Bock, Yogish C. Kudva, Scott W. Lee, Caroline Yovanovich, John J. Shin, Toni L. Cordero, Jennifer J. F. McVean, Robert A. Vigersky

PMC · DOI: 10.3389/fendo.2025.1716587 · Frontiers in Endocrinology · 2025-12-19

## TL;DR

Automated insulin delivery improved blood sugar control and reduced hypoglycemia compared to daily injections in people with type 1 diabetes.

## Contribution

A large international trial shows automated insulin delivery is safer and more effective than multiple daily injections in managing type 1 diabetes.

## Key findings

- Automated insulin delivery significantly reduced HbA1c levels compared to multiple daily injections.
- Automated systems reduced time spent in hypoglycemia compared to traditional injection methods.
- Rates of severe hypoglycemia and diabetic ketoacidosis were low and met safety criteria for automated systems.

## Abstract

This study evaluated 6-month effectiveness and safety of automated insulin delivery (AID) in comparison with multiple daily injections (MDI) in pediatric and adult type 1 diabetes (T1D).

Individuals with T1D, aged 2–80 years, were enrolled across 32 international centers (in the United States, Europe, Canada, and New Zealand) and randomized 1:1 to AID intervention (MiniMed™ 670G or 770G system) or MDI with or without continuous glucose monitoring. Primary endpoints were change in mean HbA1c for participants with a baseline HbA1c >8.0% (Group 1) and percentage of time spent below 70 mg/dL (%TBR <70 mg/dL [<3.9 mmol/L]) for participants with baseline HbA1c ≤8.0% (Group 2), to show superiority of AID intervention versus MDI. Safety endpoints including rates of severe hypoglycemia and diabetic ketoacidosis (DKA), and difference in diabetes treatment satisfaction score were assessed.

For Group 1, N = 56 participants (aged 29.4 ± 17.0 years) were randomized to AID intervention and N = 54 participants (aged 36.8 ± 19.6 years) were randomized to MDI. For Group 2, N = 73 (aged 37.4 ± 21.0 years) and N = 69 (aged 39.2 ± 19.3 years), respectively, were randomized to AID and MDI. Change in HbA1c (mean [95% CI] difference of −0.7% [−1.1, −0.3], P = 0.0002) and difference in %TBR <70 mg/dL (4.8% [−6.4, −3.1], P<0.001) favored AID intervention versus MDI. Rates of severe hypoglycemia (AID: 1.82/100 patient-years) and DKA (MDI: 3.52/100 patient-years) were low and met preestablished success criteria for safety.

This large, international, multicenter randomized controlled trial demonstrates safety of the MiniMed™ 670G/770G systems. AID significantly improved HbA1c and time spent in hypoglycemia when compared with MDI, in both youth and adults living with T1D.

## Linked entities

- **Diseases:** type 1 diabetes (MONDO:0005147), hypoglycemia (MONDO:0004946), diabetic ketoacidosis (MONDO:0012819)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** diabetes (MESH:D003920), DKA (MESH:D016883), hypoglycemia (MESH:D007003), T1D (MESH:D003922)
- **Chemicals:** glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12757873/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12757873/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12757873/full.md

---
Source: https://tomesphere.com/paper/PMC12757873