Carr, Alice L. J.
Sutton, Hannah
Agesen, Rikke M.
Bonifacio, Ezio
Bosi, Emanuele
Gillard, Pieter
Swaby, Rabbi
Vercauteren, Jurgen
Besser, Rachel E. J.
Funding for this research was provided by:
European Federation of Pharmaceutical Industries and Associations
BreakthroughT1D
European Union’s Horizon Europe
Leona M. and Harry B. Helmsley Charitable Trust
Innovative Health Initiative Joint Undertaking (101132379)
Vaccines Europe
UK Research and Innovation
MedTech
European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry
NIHR Oxford Biomedical Research Centre
JDRF/Wellcome Strategic Award (4-SRA-2017-473-A-N)
JDRF/Wellcome Strategic Award (107212/A/15/Z)
EuropaBio
Article History
Received: 14 October 2025
Accepted: 27 January 2026
First Online: 9 March 2026
Funding
: ALJC is supported by the Critical Path Institute, Breakthrough T1D, the Charles A. Allard Chair in Diabetes Research, the Blanch family, the Alberta Diabetes Institute and the Chan family. REJB, EBon, EBos, PG and JV are supported by European action for the Diagnosis of Early Non-clinical Type 1 diabetes For disease Interception (EDENT1FI). REJB additionally receives support from the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC) and a JDRF/Wellcome Strategic Award (4-SRA-2017-473-A-N; 107212/A/15/Z). RS was supported by the Novo Nordisk UK Research Foundation through a research fellowship. EDENT1FI is supported by the Innovative Health Initiative Joint Undertaking (IHI JU) under grant agreement no 101132379. The JU receives support from the European Union’s Horizon Europe research and innovation programme, the Leona M. and Harry B. Helmsley Charitable Trust, Breakthrough T1D, EFPIA, COCIR, Vaccines Europe EuropaBio and MedTech. Additional funding is provided to associated UK partners through the UK Research and Innovation (UKRI) Guarantee Fund. Views and opinions expressed are those of the author(s) only and do not necessarily reflect those of the European Union, the private members and contributing partners of the IHI JU, the NHS, the NIHR or the Department of Health or other aforementioned parties. The aforementioned parties cannot be held responsible for them.
: REJB reports receiving speaker honoraria from Eli Lilly and Springer Healthcare, sitting on the Novo Nordisk UK Foundation Research Selection Committee on a voluntary basis and acting as an independent advisor for Provent Bio, and has received speaking honoraria from Sanofi and Medscape that were donated to an education research fund. RS has received speaker honoraria for type 1 diabetes-related symposia sponsored by Sanofi. RMA is an employee and shareholder of Novo Nordisk A/S. PG’s institution has received grants from Novo Nordisk, Sanofi, Dexcom, Tandem, Medtronic, Abbott and Roche. In addition, PG has received consultancy fees from Abbott, Medtronic and Bayer; payments or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing or educational events from Medtronic, Novo Nordisk, Abbott, Ypsomed, Vitalaire, Dexcom, Bayer and Insulet; support for attending meetings and/or travel from Sanofi, Novo Nordisk, Medtronic and Roche; and payments for participation on advisory boards from Insulet, Dexcom, Tandem and Ypsomed. Additionally, PG’s institution has received equipment including Dexcom CGMs for the ALERTT1 trial and Medtronic 780G devices for the CRISTAL trial from the respective sponsors. JV presented the EDENT1FI programme at the Medtronic industry symposium at the 61st Annual Meeting of the EASD in 2025. JV is a member of Sanofi’s Advisory Committee for the BR1DGE programme. JV also serves on the Steering Committee of Sanofi’s TH1NK Ahead initiative. The authors declare that there are no other relationships or activities that might bias, or be perceived to bias, their work.
: All authors were responsible for drafting the article and reviewing it critically for important intellectual content. All authors approved the version to be published.