Eupraxia Reports Positive EoEHSS Sub-Score Data in Phase 1b/2a RESOLVE Trial

  • Eupraxia Pharmaceuticals released EoEHSS sub-score data from its ongoing Phase 1b/2a RESOLVE trial for eosinophilic esophagitis (EoE) at Digestive Disease Week.
  • EoEHSS sub-scores for inflammation showed improvements across all cohorts at 12 and 36 weeks.
  • EoEHSS sub-scores for tissue architecture (fibrosis) improved in most cohorts at 12 and 36 weeks.
  • The highest dose cohort (Cohort 9) demonstrated the largest improvements, with over 90% improvement in inflammation and over 83% in fibrosis.

Eupraxia's positive EoEHSS sub-score data from the RESOLVE trial highlights the potential of its Diffusphere technology to deliver targeted, extended-release treatments for EoE. The results suggest a significant step forward in addressing the unmet medical need in EoE, a disease affecting over 450,000 people in the U.S. The strategic focus on local, controlled drug delivery could position Eupraxia as a key player in the inflammatory gastrointestinal disease space.

Clinical Efficacy
How sustained improvements in EoEHSS sub-scores will impact the Phase 2b portion of the RESOLVE trial.
Dose Optimization
Whether the highest dose (Cohort 9) will be the focus of future trials and regulatory filings.
Market Differentiation
The pace at which Eupraxia can position EP-104GI as a differentiated treatment for EoE.