An open-label extension multi-centre trial in adult subjects diagnosed with Type 1 diabetes mellitus exploring the effect of long-term Verapamil SR therapy on the preservation of beta-cell function.
Recipient organisationNIHR Sheffield Biomedical Research Centre
NIHR supportRecorded as supported by this research centre
PeriodFeb 2025 — May 2027
In plain English
AI plain-English summary
A daily 360 mg dose of Verapamil SR, a common blood pressure drug, is being tested to see if it can preserve insulin production in adults newly diagnosed with Type 1 diabetes. Type 1 diabetes destroys the pancreas’s beta cells, which produce insulin. Patients must inject insulin for life, but even with careful management, blood sugar control is imperfect. Previous animal and human studies suggest Verapamil may protect these remaining beta cells, allowing the body to produce some of its own insulin. The Ver-A-Long study will test this over 24 months in adults, measuring whether beta-cell function is preserved and whether the drug is safe for long-term use. If Verapamil proves effective, it could change the standard of care for newly diagnosed Type 1 diabetes. Patients might need less injected insulin, experience fewer dangerous blood sugar swings, and face a lower risk of long-term complications like kidney disease or blindness. This would not be a cure, but a practical, repurposed drug that improves daily disease management and long-term health outcomes.
View original technical description
Verapamil SR (sustained release), a medication used for high blood pressure, has been shown to help beta cells in the pancreas produce more insulin. This may help in managing Type 1 diabetes (T1D). Previous studies in animals and humans with newly diagnosed T1D suggest that Verapamil could improve beta-cell function, reduce the need for insulin, and potentially prevent or reverse the disease. The Ver-A-Long study aims to explore whether long-term treatment with Verapamil SR (360 mg daily) can help preserve beta-cell function in adults with T1D and evaluate its safety over 24 months.
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