-- Eupraxia Pharmaceuticals (EPRX.TO) 周二公布了 Resolve 试验剂量递增部分最高剂量组的最新 36 周结果。 该公司表示,与基线水平相比,第 9 组患者在组织健康和症状缓解方面均表现出“显著”改善。第 9 组患者在第 36 周时症状临床缓解率达到 66%。声明补充道,该缓解水平在第 8 周首次达到,并持续至第 36 周。 Resolve 试验是一项多中心、剂量递增研究,旨在测试 Eupraxia 的 EP-104GI 治疗活动性嗜酸性粒细胞性食管炎 (EoE) 成人患者的疗效和安全性。该疗法通过 4 至 20 次食管壁注射单次给药,患者对该药物的耐受性良好。 “这些数据与我们此前在该剂量水平下观察到的显著结果一致,凸显了单次注射EP-104GI后即可获得强效且持久疗效的潜力。此外,试验中所有剂量组的安全性均表现优异,我们持续未观察到任何与药物相关的严重不良事件(SAE)或血糖、皮质醇水平的显著升高,这令我们倍感欣慰。”首席执行官詹姆斯·哈利韦尔博士表示。 Resolve试验2b期部分的主要数据预计将于今年第四季度公布。 周一,Eupraxia股票在多伦多证券交易所收盘上涨0.16美元,至9.90美元。
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