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Senseonics Holdings, Inc. Announces Data From the Eversense® Post Approval Study to Be Presented at the 17th International Conference on Advanced Technologies and Treatments for Diabetes
GERMANTOWN, Md.--(BUSINESS WIRE)-- Senseonics Holdings, Inc. (NYSE American: SENS), a medical technology company focused on the development and manufacturing
About this update from Senseonics Holdings, Inc.
[{"type":"text","content":" GERMANTOWN, Md.--(BUSINESS WIRE)--\nSenseonics Holdings, Inc. (NYSE American: SENS), a medical technology company focused on the development and manufacturing of long-term, implantable continuous glucose monitoring (CGM) systems for people with diabetes, today announced data from the Eversense® Post Approval Study is to be presented at the 17th International Conference on Advanced Technologies and Treatments for Diabetes (“ATTD”) in Florence, Italy.\n\n\nDr. Kashif Latif, Principal Investigator, Medical Director, and practicing physician in Endocrinology from AM Diabetes & Endocrinology in Bartlett, TN, is scheduled to give an oral presentation on People Reported Outcomes (“PROs”) from the U.S. Eversense Post Approval Study on Saturday, March 09, 2024 at 11:30 CET at Fortezza da Basso, Hall D.\n\n\n“This study is the first real-world evaluation of how people using Eversense feel about their diabetes and how Eversense helps them manage their condition over two years of repeated sensor insertions and removals. We are pleased the data shows high satisfaction scores, improved diabetes distress scores, and no evidence that repeated insertions and removals impact satisfaction,” said Francine Kaufman, M.D., Chief Medical Officer of Senseonics. “As patients and providers consider the best options to help manage diabetes, presenting this additional compelling data continues to raise the awareness of the benefits of Eversense. We look forward to sharing the results with our colleagues at ATTD.”\n\n\nThe Post Approval Study was a prospective, multicenter 2-year evaluation of Eversense CGM System use in adults 18 years of age and older with either type 1 or 2 diabetes (T1D or T2D). Participants were initially inserted with the 90-day Eversense CGM System and then transitioned to the 180-day Eversense E3 CGM System after approval in 2022, in accordance with labeling at the time over their 2 years of study participation. The DDS-17 (a questionnaire designed to measure four critical dimensions of distress with diabetes: emotional burden, regimen distress, interpersonal distress and physician distress) was administered to participants at the start of the study. Both the DDS-17 and CGM-Sat (a 44-item questionnaire designed to measure the impact of using CGM on diabetes management and family relationships regarding satisfaction with emotional, b...