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ID 69625
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Kamiya, Hideki Division of Diabetes, Department of Internal Medicine, Aichi Medical University School of Medicine
Suzuki, Ryo Department of Diabetes, Metabolism and Endocrinology, Tokyo Medical University
Wada, Jun Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University ORCID Kaken ID publons researchmap
Deguchi, Takahisa Department of Diabetes, Metabolism and Endocrinology, Kagoshima University Graduate School of Medical and Dental Sciences
Himeno, Tatsuhito Division of Diabetes, Department of Internal Medicine, Aichi Medical University School of Medicine
Yamamoto, Shuhei Data Intelligence Department, Daiichi Sankyo Co., Ltd.
Toyama, Taiki Primary Medical Science Department, Daiichi Sankyo Co., Ltd.
Nakamura, Jiro Division of Diabetes, Department of Internal Medicine, Aichi Medical University School of Medicine
Abstract
Background/Objectives: The exact prevalence of and recent changes in diabetic polyneuropathy (DPN) and diabetic peripheral neuropathic pain (DPNP) in Japan are unclear. The oral gabapentinoid, mirogabalin besylate (mirogabalin), is effective with a good safety profile for DPNP with moderate-to-severe pain (numerical rating scale [NRS] scores ≥ 4). However, clinical evidence for mild pain (NRS scores ≤ 3) is unclear. The Dia-NeP study aims to examine: (1) the prevalences of DPN and DPNP and background factors in patients with type 2 diabetes mellitus (T2DM); and (2) the efficacy and safety of mirogabalin in patients with DPNP, including those with mild pain.
Methods: The Dia-NeP study is a multicenter, prospective study consisting of two parts, a baseline survey and an interventional study, to be conducted from March 2025 to August 2026 in patients with T2DM in Japan. The baseline survey is the observational study investigating the epidemiology of DPN and DPNP, and the interventional study is an exploratory, single-arm, open-label study of 12-week mirogabalin treatment. Of patients with T2DM enrolled in the baseline survey, those diagnosed with DPNP who have an NRS score for pain ≥ 1 will be included in the interventional study. The target sample size is 1000 to 3000 patients for the baseline survey and 100 for the interventional study.
Planned Outcomes: The primary endpoint is the change from baseline in the NRS score at week 12 in the interventional study. The safety endpoint is adverse events. This study will not only show the latest prevalence of DPN and DPNP in Japan, but is also the first study to investigate the efficacy and safety of mirogabalin in patients with DPNP having mild pain, as well as moderate-to-severe pain, and is expected to provide useful evidence for future DPN and DPNP treatment.
Trial Registration: Japan Registry of Clinical Trials (jRCTs031240623, registered 20/January/2025, https://jrct.mhlw.go.jp/en-latest-detail/jRCTs031240623).
Keywords
Diabetic peripheral neuropathic pain
Diabetic polyneuropathy
Epidemiological survey
Exploratory study
Mirogabalin
Quality of life
Published Date
2025-10-24
Publication Title
Diabetes Therapy
Volume
volume16
Issue
issue12
Publisher
Springer Science and Business Media LLC
Start Page
2351
End Page
2363
ISSN
1869-6953
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2025
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Web of Science KeyUT
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isVersionOf https://doi.org/10.1007/s13300-025-01809-5
License
http://creativecommons.org/licenses/by-nc/4.0/
Citation
Kamiya, H., Suzuki, R., Wada, J. et al. A Multicenter, Prospective, Observational, and Single-Arm Interventional Study of Mirogabalin in Diabetic Peripheral Neuropathic Pain: Rationale and Design of Dia-NeP. Diabetes Ther 16, 2351–2363 (2025). https://doi.org/10.1007/s13300-025-01809-5
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( 第一三共株式会社 / Daiichi Sankyo Co., Ltd. )