Key Highlights
- Eupraxia Pharmaceuticals shared new RESOLVE trial data for EP-104GI in eosinophilic esophagitis.
- Moderate-to-severe odynophagia rates fell from 62% at baseline to just 25% by weeks 24-52.
- Half of patients reported zero pain upon swallowing by the one-year mark.
- The data underscore a significant and lasting reduction in disease-related symptom burden.
Eupraxia Pharmaceuticals Inc. (NASDAQ: EPRX) shared a fresh look at its RESOLVE trial for EP-104GI in eosinophilic esophagitis, revealing that moderate-to-severe odynophagia rates plunged from 62% at baseline to just 25% by weeks 24 to 52.
What Happened
With half of the patients reporting zero pain upon swallowing by the one-year mark, the data underscore a significant and lasting reduction in disease-related symptom burden.
Market Reaction
The disclosed information does not include stock price or trading data for Eupraxia Pharmaceuticals following the RESOLVE trial update.
Outlook
Continued follow-up on the durability of symptom reduction observed in the RESOLVE trial is likely to remain relevant as Eupraxia Pharmaceuticals advances EP-104GI in eosinophilic esophagitis.
FAQs
Q: What did the RESOLVE trial show for EP-104GI?
A: Moderate-to-severe odynophagia rates fell from 62% at baseline to just 25% by weeks 24-52, with half of patients reporting zero pain upon swallowing at one year.
Q: What condition is EP-104GI being developed to treat?
A: Eosinophilic esophagitis.
Q: What does odynophagia refer to in this trial?
A: Pain upon swallowing, a key symptom measured in the RESOLVE trial.
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