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Syntara公司骨髓癌治疗临床试验获得美国FDA积极反馈

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-- Syntara(ASX:SNT)周二向澳大利亚证券交易所提交的文件显示,在一次C类会议上,美国食品药品监督管理局(FDA)给予了积极反馈,支持其针对骨髓纤维化治疗药物amsulostat的2b期临床试验方案设计。 该文件指出,该2b期临床试验的主要终点是治疗9个月后总症状评分降低50%,预计将招募约100名患者。 该公司表示,美国FDA的积极反馈使得amsulostat得以进入后期临床开发阶段,并为与潜在商业伙伴的进一步合作铺平了道路。 骨髓纤维化是一种骨髓癌,其特征是瘢痕组织的积聚导致红细胞、白细胞和血小板减少。

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