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789
新冠肺炎主要侵袭肺脏,新药可改善发炎状况、修复细胞,可望成为治疗新希望。
随著新冠肺炎疫情持续扩大,死亡人数不断攀升,现在又出现新药治疗希望!宣捷细胞生物制药由脐带间质干细胞所研发的新药UMC119-06,原本用于治疗急性呼吸窘迫症候群,先后通过卫福部及美国食品药物管理局(FDA)核准可进行临床一期试验,成为全台唯一研发中新药被核准执行治疗急性和慢性肺病临床一期试验的细胞新药公司,不但为目前新冠肺炎患者带来治疗新希望,也等于替台湾抗疫增添一道防线。
根据中国周二统计,新冠肺炎确诊病例高达4万2708例,死亡病例1017宗,重症患者会因免疫系统受到病毒感染伤害,淋巴细胞减少,免疫力失调、抵抗力下降而引发肺炎,是新冠肺炎患者死亡的主要原因之一。
对此,宣捷制药多年来专注于人类脐带间质干细胞新药研发,其中同种异体研发中新药UMC119-06原本用于治疗慢性阻塞性肺疾病(COPD)和ARDS新药临床试验(IND)审查核准。由于脐带间质干细胞具有增进内源干细胞生长与分化,以及免疫调节的药物作用机制,从动物功效性试验发现,UMC119-06注射至慢性发炎小鼠,结果证实能改善肺脏发炎,降低全身性发炎因子,组织切片显示具有改善肺泡结构和肺气肿之功效。另外,注射至急性肺损伤小鼠,不仅能改善小鼠肺脏的过度炎症,对于受损的肺泡组织及肺水肿具有显著的修复作用,由此可见,UMC119-06具有治疗急慢性肺病的潜力,无疑替目前无药可医的新冠肺炎患者带来治疗新希望。
宣捷制药董事长宣昶有表示,研发团队将秉持人溺己溺,兼善天下之胸怀,全力配合政府阻止疫情加重的一切努力,若卫福部需要UMC119-06细胞新药用于新冠肺炎患者之治疗,宣捷制药将履行研发细胞新药,造福全球病患之企业社会责任,必将戮力配合。
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