联邦制药(03933.HK)UBT251注射液获美FDA批准新药临床试验

阿斯达克财经
04 Mar

联邦制药(03933.HK) 公布,全资附属联邦生物科技(珠海横琴)自主研发的1类创新药UBT251注射液获美国药品监督管理局“FDA”许可,同意开展慢性肾脏病“CKD”适应症II期临床试验。此前,CKD适应症已获得中国国家药品监督管理局临床试验批准。(de/d)(港股报价延迟最少十五分钟。沽空资料截至 2025-03-03 16:25。)

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