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Acknowledgements
Funding
No funding or sponsorship was received for this study or publication of this article.
Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Author Contributions
Nomoto H had the idea for the article. Oe Y and Nomoto H wrote the manuscript. Miya A, Kameda H, Cho KY, Nakamura A, Miyoshi H, and Atsumi T critically revised the manuscript.
Disclosures
This study received no specific financial support. Nakamura A has obtained research support from Mitsubishi Tanabe Pharma, Nippon Boehringer Ingelheim Co., Kissei Pharmaceutical Co., Ltd., and Taisho Pharmaceutical Co., Ltd. Cho KY has received honoraria for lectures from Eli Lilly Japan K.K. Miyoshi H has received honoraria for lectures from Astellas Pharma Inc., Sumitomo Dainippon Pharma Co., Ltd., Eli Lilly Japan K.K., Mitsubishi Tanabe Pharma Co., MSD K.K., Novo Nordisk Pharma Ltd., Kowa Pharmaceutical Co., Ltd., Nippon Boehringer Ingelheim Co., Ono Pharmaceutical Co., Ltd., and Sanofi; and has received research funding from Astellas Pharma Inc., Daiichi Sankyo Co., Sumitomo Dainippon Pharma Co. Ltd., Eli Lilly Japan K.K., Mitsubishi Tanabe Pharma Co., Novo Nordisk Pharma, Kowa Pharmaceutical Co., Ltd., Abbott Japan Co., Nippon Boehringer Ingelheim Co., Ono Pharmaceutical Co., Ltd., LifeScan Japan Inc., and Taisho Pharmaceutical Co., Ltd. Atsumi T has received research grants from Astellas Pharma Inc., Takeda Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Co., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co. Ltd., Otsuka Pharmaceutical Co., Ltd. Pfizer Inc., Alexion Inc., Ono Pharmaceutical Co., Ltd., and Teijin Pharma Ltd.; speaking fees from Mitsubishi Tanabe Pharma Co., Chugai Pharmaceutical Co., Ltd., Astellas Pharma Inc., Takeda Pharmaceutical Co., Ltd., Pfizer Inc., AbbVie Inc., Eisai Co. Ltd., Daiichi Sankyo Co., Ltd., Bristol-Myers Squibb Co., UCB Japan Co. Ltd., Eli Lilly Japan K.K., Novartis Pharma K.K., Eli Lilly Japan K.K., Kyowa Kirin Co., Ltd., and Taiho Pharmaceutical Co., Ltd.; and fees for consultancies from AstraZeneca plc., Medical & Biological Laboratories Co., Ltd., Pfizer Inc., AbbVie Inc., Ono Pharmaceutical Co. Ltd., Novartis Pharma K.K., and Nippon Boehringer Ingelheim Co., Ltd. Oe Y, Nomoto H, Miya A and Kameda H have no conflicts of interest to declare.
Compliance with Ethics Guidelines
This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors. The original study was registered with the University Hospital Medical Information Network (UMIN) (registration number UMIN 000039460) and approved by the Institutional Review Board of Hokkaido University Hospital Clinical Research and Medical Innovation Center (019-0293).
Data Availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Oe, Y., Nomoto, H., Miya, A. et al. Letter to the Editor Regarding Efficacy of IDegLira Versus IDegAsp Therapy in Patients with Type 2 Diabetes: A Randomized Crossover Study by isCGM. Adv Ther 40, 383–386 (2023). https://doi.org/10.1007/s12325-022-02327-7
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DOI: https://doi.org/10.1007/s12325-022-02327-7