Advancing EoE Care Through Innovation, Collaboration, and Real-World Impact
In 2024, the U.S. Food and Drug Administration (FDA) approved two drugs for patients with eosinophilic esophagitis (EoE)—Dupixent® (dupilumab) in children as young as 1 year of age and Eohilia™ (budesonide oral suspension) in children 11 years and older. Thanks to discoveries from the Cincinnati Center for Eosinophilic Disorders (CCED), researchers now understand more of the basic science behind these drugs’ novel mechanisms of action.
The CCED is one of the first and largest eosinophilic disease programs in the world. As a dedicated research hub, the center plays a pivotal role in several multicenter clinical trials, including the two that resulted in these FDA wins. The seamless interaction between clinical care and research that the CCED fosters helps drive the basic understanding of how these diseases work and keeps the focus on patient and family needs to improve their care.
“We know that a lot of what we’ve done for patients for years works,” explains Vince Mukkada, MD, site principal investigator and author on the budesonide studies. “But we want to push the envelope forward and ask, ‘Are there new approaches that might be novel or offer real advantages to our patients?’ We are constantly trying to advance the field and improve what we do.”