Core Insights - Eupraxia Pharmaceuticals Inc. has provided an operational update on the development of EP-104GI, reporting data from Cohort 9 of the RESOLVE trial, where patients received an 8mg dose per injection for the first time [1][2] Clinical Trial Results - Cohort 9 demonstrated the largest improvements in tissue health outcomes and eosinophil reduction to date, with no serious adverse events reported [5][6] - The RESOLVE Safety Committee endorsed the 8mg dose as the second dose for the ongoing Phase 2b study, indicating strong confidence in the dosing strategy [5][6] - The company plans to expand the Phase 2b study from 60 to at least 120 patients, enhancing the statistical power and safety database [8][13] Future Plans - Eupraxia intends to initiate a clinical trial for an additional gastrointestinal indication in the first half of 2026, leveraging recent financing to support this expansion [5][8] - The company aims to disclose additional data from the RESOLVE trial in Q4 2025 and expects top-line data from the Phase 2b trial in Q3 2026 [9][16] Technology and Market Potential - EP-104GI utilizes Eupraxia's proprietary Diffusphere™ technology for localized drug delivery, which may improve safety and efficacy compared to traditional methods [15][16] - Eosinophilic Esophagitis (EoE) affects over 450,000 people in the U.S., indicating a significant market opportunity for effective treatments [11][16]
Eupraxia Pharmaceuticals Announces Positive Data from Highest-Dose Cohort in the Ongoing RESOLVE Trial in Eosinophilic Esophagitis, and Plans for Expansion of EP-104GI Development Programs