logo
Vogenx, Inc. to Present Phase 2 Clinical Data on Mizagliflozin at the Endocrine Society (ENDO) 2025 Annual Conference

Vogenx, Inc. to Present Phase 2 Clinical Data on Mizagliflozin at the Endocrine Society (ENDO) 2025 Annual Conference

Data from Phase 2 Trial VGX-001-012 of Mizagliflozin in Post Bariatric Hypoglycemia will be Presented
RALEIGH, NC / ACCESS Newswire / April 15, 2025 / Vogenx, Inc., a clinical-stage developer of novel therapeutics for the treatment of serious metabolic and gastrointestinal diseases, today announced that it will present phase 2 clinical data from Study VGX-001-012 (NCT05721729) at the Endocrine Society (ENDO) 2025 Annual Conference highlighting Mizagliflozin's effect on hypoglycemic events and relevant pharmacodynamic indicators in patients diagnosed with post bariatric hypoglycemia (PBH). Vogenx will present the data during an oral presentation during the ENDO 2025 Conference which will take place July 12-15, 2025 in San Francisco, California.
Abstract Number: 3890
Title: Efficacy and Safety of the SGLT1 Inhibitor Mizagliflozin in Patients with Post-Bariatric Hypoglycemia
Presentation Type: Oral
Session Date & Time: Saturday Jul 12, 2025; 1:45 PM - 3:15 PM
Location: Moscone Convention Center, 747 Howard St, San Francisco, CA 94103
Additional details will be made available prior to the Conference.
About Mizagliflozin
Mizagliflozin is an investigational first-in-class, oral, small molecule drug candidate that reduces postprandial glucose absorption, secretion of insulin, and secretion of gastric inhibitory peptide, also known as glucose-dependent insulinotropic peptide (GIP). The molecule is being developed by Vogenx for the treatment of PBH and gastroparesis, both debilitating diseases with high unmet medical need in underserved patient populations. Mizagliflozin has shown statistically significant reductions in Level 3 hypoglycemia events, postprandial glucose absorption as well as secretion of insulin and GIP in patients diagnosed with PBH.
About Post-Bariatric Hypoglycemia
PBH is an increasingly recognized chronic side effect of bariatric surgeries that are commonly performed as a treatment for obesity and related comorbidities. Neuroglycopenic symptoms can include shakiness, dizziness, confusion, sweating and loss of consciousness. These symptoms can debilitate with a significant negative impact on quality of life, can dangerously impair normal day-to-day activities and can be life-threatening.
Bariatric surgery has proven to be the most effective treatment for severe obesity, leading to significant improvements in body mass index and obesity-related co-morbidities. It is estimated that over 9% of the U.S. population has a body mass index above 40 which is considered severely obese. With over 250,000 bariatric surgery procedures performed per year in the United States, postoperative prevalence of hypoglycemia symptoms in bariatric surgery patients is thought to be as high as 38.5%. There are currently no therapeutics approved by the FDA for the treatment of PBH.
About Vogenx, Inc.
Vogenx, Inc. is a clinical-stage life science company based in Raleigh, North Carolina. Vogenx is focused on developing novel therapeutics for the treatment of serious metabolic and gastrointestinal diseases with high unmet medical need. The company is developing Mizagliflozin for post bariatric hypoglycemia and gastroparesis. For more information about Vogenx, please visit https://vogenx.com.
For more information:
+1 919.659.5677
[email protected]
SOURCE: Vogenx, Inc.
press release

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Applied Medical Technology, Inc. Unveils Redesigned Mobile App Aligned with Recent Website Refresh
Applied Medical Technology, Inc. Unveils Redesigned Mobile App Aligned with Recent Website Refresh

Yahoo

time11 minutes ago

  • Yahoo

Applied Medical Technology, Inc. Unveils Redesigned Mobile App Aligned with Recent Website Refresh

BRECKSVILLE, Ohio., June 10, 2025 /PRNewswire/ -- Applied Medical Technology, Inc. (AMT), a leader in innovative medical devices, is proud to announce the launch of its redesigned mobile application, AMT ONE Source®. This strategic update follows a successful website redesign completed late 2024, ensuring that both platforms now offer a cohesive, user-friendly digital experience. Enhancing User Experience Across PlatformsThe redesigned mobile app mirrors the modern, intuitive design language introduced during the website refresh. With a renewed focus on user experience and engagement, the mobile platform now features streamlined interfaces and updated information. "In today's fast-paced healthcare environment, it is essential that our digital platforms are not only reliable but also easy to navigate and visually appealing," said Bill Bentley, National Sales Manager. "Created with our youngest patients in mind, the redesign was thoughtfully developed to be more engaging, age-appropriate, and easy to navigate—helping children and their families feel more supported and empowered throughout their healthcare journey." Key Features and Benefits Unified Design Aesthetic: The mobile app adopts the clean, modern design previously launched on the website, providing a consistent look and feel across all digital touchpoints. Richer Content Experience: The app now features an expanded content database, providing a broader range of resources and information to support users with timely, relevant, and easy-to-access content. Improved Performance: The redesigned app features enhanced performance, with a new backend architecture that allows for faster content updates, easier maintenance, and more frequent improvements to keep the experience fresh and relevant. AMT partnered with Cleveland-Ohio based software company, Stream 9, on the redesign. Their strong track record in software design and development brought deep technical expertise and a strategic approach. "We're fortunate in our business to develop custom software projects for businesses of all kinds; but it's especially rewarding to work on a project that will deliver such a direct benefit to patients and their caregivers. AMT brought a clear vision to the table, and we worked closely together to translate that into a modern, scalable, and user-friendly digital experience," shared Kirk Miesle, Founder of Stream 9. The AMT ONE Source® app is available now on the App Store and Google Play. About AMT: Applied Medical Technology, Inc. (AMT) is a global leader in enteral and surgical devices committed to improving lives through innovation. For 40 years, AMT has bridged the gap between medical technology and patient needs, collaborating with healthcare professionals and users to develop high-quality, life-enhancing solutions. Our holistic approach prioritizes the well-being of the whole person, not just the device they use. View original content to download multimedia: SOURCE Applied Medical Technology, Inc. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Pennsylvania lawmakers advance bill expanding no-cost breast cancer diagnostics
Pennsylvania lawmakers advance bill expanding no-cost breast cancer diagnostics

Yahoo

time25 minutes ago

  • Yahoo

Pennsylvania lawmakers advance bill expanding no-cost breast cancer diagnostics

HARRISBURG, Pa. (WHTM) — Pennsylvania was one of the first states to require insurance companies to cover breast cancer screenings for high-risk women. Now, lawmakers want to expand on the law. Senate Bill 88 passed out of the insurance committee unanimously on Tuesday. The bill would clarify that insurance companies must cover screenings and diagnostics with no out-of-pocket costs for not just high-risk women but average-risk women, too. Close Thanks for signing up! Watch for us in your inbox. Subscribe Now That covers just about everyone. Governor Josh Shapiro signed Act 1 into law in 2023 as the first bill of his administration. The law, which unanimously passed the Senate and House, required insurance companies to pay for preventative care such as genetic testing, MRIs, and ultrasounds for women at high risk of breast cancer. Insurance companies covered the screenings, but some still charged women for diagnostics if something was found. Governor Shapiro signs historic breast cancer screening bill 'But we know that screening is just one part of early detection, and far too many patients are still being hit with costs for the diagnostic imaging they need next,' said Senate President Pro Tempore Kim Ward (R-Westmoreland), who co-sponsored the bill. 'It's time to finish what we started and make sure every woman has access to the full range of breast imaging, including diagnostic exams, without cost standing in the way.' The bill now heads to the Senate for consideration, where it is likely to pass. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store