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Optimizing Obesity Trials: Integrating Diverse Endpoints to Holistically Assess Safety and Efficacy of GLP-1 Agonists and Beyond, Upcoming Webinar Hosted by Xtalks

Tuesday, October 22, 2024 Obesity News
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PR Newswire

TORONTO, Oct. 22, 2024

In this free webinar, learn about how obesity and diabetes drug development requires monitoring for hypoglycemia with a blood glucose meter (BGM) for regulatory submission. Attendees will learn how GLP-1 agonists and other obesity drugs can change body composition, liver fat density and the brain's response to food cues. The featured speakers will discuss how loss of muscle poses a significant health risk for individuals experiencing weight loss. The speakers will also share how obesity drug trials often include patients with pre-existing cardiovascular disease, which requires robust cardiac safety testing.
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TORONTO, Oct. 22, 2024 /PRNewswire-PRWeb/ -- An estimated 1 billion people are living with obesity worldwide, with adult obesity rates having doubled since 1990 and quadrupled in children and adolescents. Individuals with obesity are at an increased risk of cardiovascular disease, diabetes and certain cancers, among other comorbidities. This increased prevalence, combined with the clinical and commercial success of glucagon-like peptide (GLP)-1 agonists for treating both obesity and diabetes, has led to a multitude ofmany clinical trials assessing the safety and efficacy of new therapies.
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With these studies, researchers are identifying risks and benefits across health disciplines, including cardiovascular, metabolic, mental health, sleep, endocrine and gastrointestinal impacts. For these reasons, it is essential for drug manufacturers to incorporate comprehensive assessments of safety and efficacy to obtain regulatory approval and maximize market opportunities by generating robust data supporting secondary efficacy claims.

Designing a holistic obesity trial is complex due to the need for endpoints across multiple disciplines, including medical imaging, electronic outcomes assessments and cardiac endpoints for efficacy and safety:

Register for this webinar today to delve into the intricacies of designing holistic obesity trials that incorporate multi-disciplinary endpoints.

Join experts from Clario, Todd Rudo (Moderator), MD, Chief Medical Officer; Paul Strumph, MD, Diabetes & Metabolism Key Opinion Leader, Clinical Science & Consulting; Fabian Chen, MD, VP and Deputy CMO, Cardiology; and Mark W. Tengowski, DVM, MS, PhD, Director Medical & Scientific Affairs, Medical Imaging, for the live webinar on Tuesday, November 12, 2024, at 11am EST (4pm GMT/UK).

For more information, or to register for this event, visit Optimizing Obesity Trials: Integrating Diverse Endpoints to Holistically Assess Safety and Efficacy of GLP-1 Agonists and Beyond.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars and digital content to the global life science, food, healthcare and medical device communities. Every year, thousands of industry practitioners (from pharmaceutical, biotechnology, food, healthcare and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps professionals stay current with industry developments, regulations and jobs. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit https://xtalks.com For information about hosting a webinar visit https://xtalks.com/why-host-a-webinar/

Contact: Vera Kovacevic Tel: +1 (416) 977-6555 x371 Email: [email protected]

Media Contact

Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, [email protected], www.xtalks.com

View original content to download multimedia:https://www.prweb.com/releases/optimizing-obesity-trials-integrating-diverse-endpoints-to-holistically-assess-safety-and-efficacy-of-glp-1-agonists-and-beyond-upcoming-webinar-hosted-by-xtalks-302282724.html

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