Rossi, Maria Chiara http://orcid.org/0000-0001-8696-4238
Bonfanti, Riccardo
Graziano, Giusi
Larosa, Monica
Lombardo, Fortunato
Nicolucci, Antonio
Vespasiani, Giacomo
Zucchini, Stefano
Rabbone, Ivana
Bracciolini, G. P.
Cherubini, V.
Bobbio, A.
Zucchini, S.
Suprani, T.
De Donno, V.
Lombardo, F.
Bonfanti, R.
Franzese, A.
Rabbone, I.
Graziani, V.
Zampolli, M.
Rutigliano, I.
de Sanctis, L.
Guerraggio, L. P.
Franceschi, R.
Tornese, G.
Franco, F.
Maffeis, C.
Arnaldi, C.
,
Funding for this research was provided by:
Statistical analysis and medical writing assistance was funded by Sanofi S.r.l., Milan, Italy.
Article History
Received: 21 February 2024
Accepted: 10 May 2024
First Online: 24 May 2024
Declarations
:
: Maria Chiara Rossi and Antonio Nicolucci have received funding for research from Sanofi, NovoNordisk, Alfasigma, Pikdare, AstraZeneca, Shionogi, SOBI, and Theras. Riccardo Bonfanti has served on advisory board panels for Sanofi, Novonordisk, Lilly, Medtronic, Abbott, Movi and has received speaker’s fees by Novonordisk, Sanofi, Lilly, Movi, Medtronic, Theras and financial support for research by Movi and Lilly. Giusi Graziano has nothing to disclose. Monica Larosa is an employee of Sanofi and may hold shares and/or stock options in the company. Fortunato Lombardo has received consultancy fees from Movi. Stefano Zucchini has served on advisory board panels for Sanofi and Movi. Giacomo Vespasiani is medical consultant of Meteda. Ivana Rabbone has received honoraria for participating in the speaker bureau and consulting fees as a member of Eli Lilly, Menarini, Medtronic, Theras, Novo Nordisk and Sanofi advisory boards.
: All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008. The study protocol was approved by all local ethics committees of the participating centers.
: Due to the study design and the anonymous by design database, based on Italian regulations, the signature of patient informed consent was not requested.